The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index; 19 of the 43 sources its claims cite were checked for support.
Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation*
Open accessAbstract
The regulation of synthesis, degradation, and distribution of lipids is crucial for homeostasis of organisms and cells. The sterol regulatory element-binding protein (SREBP) transcription factor family is post-translationally activated in situations of reduced lipid abundance and activates numerous genes involved in cholesterol, fatty acid, and phospholipid synthesis. In this study, we provide evidence that the primary transcript of SREBP2 contains an intronic miRNA (miR-33) that reduces cellular cholesterol export via inhibition of translation of the cholesterol export pump ABCA1. Notably, miR-33 also inhibits translation of several transcripts encoding proteins involved in fatty acid β-oxidation including CPT1A, HADHB, and CROT, thereby reducing fatty acid degradation. The genetic locus encoding SREBP2 and miR-33 therefore contains a protein that increases lipid synthesis and a miRNA that prevents export and degradation of newly synthesized lipids. These results add an additional layer of complexity to our understanding of lipid homeostasis and might open possibilities for future therapeutic intervention.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
miR-33a is encoded in an intron of SREBP2 and directly represses ABCA1, CPT1A, HADHB, and CROT, thereby reducing cholesterol export and fatty acid β-oxidation while increasing cellular lipids. This bifunctional locus couples lipid synthesis with suppression of lipid export and degradation.
Key findings
- miR-33a localizes to an intron of SREBP2 and is evolutionarily conserved; reporter assays show it targets the ABCA1 3′ UTR, and seed-region mutations abolish this response.
- Overexpression of miR-33 reduces endogenous ABCA1 protein and apoAI-dependent cholesterol export in HepG2 and THP1 cells; miR-33 sponges and antagomirs increase ABCA1 protein and cholesterol export.
- miR-33 targets CPT1A, HADHB, and CROT 3′ UTRs; overexpression suppresses HADHB and CPT1A protein, reduces CROT mRNA, causes a 20% reduction in mitochondrial β-oxidation, and increases cellular free fatty acids and triacylglycerides.
- The Drosophila CPT1 3′ UTR contains a conserved functional miR-33 binding site, suggesting ancient regulation of β-oxidation.
Methods
- Reporter assays used luciferase constructs containing wild-type or mutated 3′ UTRs cotransfected with pre-miR-33 or control; lentiviral miR-33 overexpression, miRNA sponges, and antagomirs were tested in HepG2, THP1, Y1, and 293T cells, with Western blot, qPCR, and Northern blot readouts.
- Cholesterol export was measured using [1,2-3H]cholesterol and apoAI; β-oxidation was measured by conversion of [9,10-3H]palmitic acid to water in the presence or absence of etomoxir; lipids were analyzed by TLC.
- Male C57/BL6 mice were fed chow or a high-fat diet (60% calories from fat) for 16 weeks starting at 4 or 8 weeks of age; miR-33 levels were assessed by Northern blot. Analyses used normalized luciferase activity, Student’s t tests, and means ± S.D. or S.E.
Limitations
- Stated: no specific CROT Western blot was obtained; miR-33 inhibition did not reproducibly increase β-oxidation or HADHB/CPT1A protein in HepG2 cells; fasting and high-fat-diet mouse livers showed no significant miR-33 changes, with only a small non-significant trend toward lower levels on high-fat diet; preliminary TLC/gas chromatography did not support altered fatty acid chain lengths; future in vivo experiments are needed.
- Evident: many mechanistic conclusions rely on cell lines, overexpression, and reporter assays, so in vivo regulation and therapeutic relevance remain unestablished; several results are described as data not shown.
Model-written summary. Check it against the paper before relying on it.
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Verification
Claims the paper makes
19 of 43 cited sources checked · 10 supported · 0 flagged · accuracy not yet measured
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Interestingly, the dominant allosteric inhibitor malonyl-CoA regulates CROT similarly to CPT1A (28,52).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [28] Saggerson, 2008, Annu. Rev. Nutr. source
- Partly supportedcites [52] A'Bháird, 1992, Biochem. J. sourceExperimental — accuracy not yet measured
In the 'Kinetics of COT assayed in peroxisomes' section, the paper says malonyl-CoA inhibits peroxisomal COT more selectively than other short-chain acyl-CoA esters and that features of this inhibition resemble CPT-I. It does not establish that the inhibition is allosteric: a separate regulatory binding site is proposed as a possibility, while inhibition of purified COT is described as competitive. Page numbers were not supplied with these passages. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesEvery source the paper cites for this claim was checked and supports it.
In the paper
“Surprisingly, there is evidence that reduced gene dosage or activity of this enzyme complex leads to the accumulation of lipids in the liver (hepatic steatosis) (32,33).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Supportedcites [32] Ibdah, 2005, Gastroenterology source
The Discussion reports that heterozygosity for an MTP defect causes fatty liver disease in aging mice and links impaired fatty-acid oxidation to hepatic steatosis. The Results specify that steatosis developed in aging, but not young, heterozygous mice; the citing sentence's 'there is evidence' framing is consistent with that finding. (LLM, conf=0.92)
- Supportedcites [33] Kao, 2006, Hum. Mol. Genet. source
The Western blot and enzyme activity assay section reports reduced mitochondrial trifunctional protein subunits and enzyme activities in affected mice, with similar findings in liver tissue. The Histopathological analyses section reports increased lipid droplets in their hepatocytes, consistent with hepatic steatosis. The paper supports the reduced-activity part of the claim. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“As shown in Fig. 6A, miR-33 suppresses HADHB and CPT1A protein levels.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
- Rests on an assumption: The antibodies used for Western blot analysis specifically detect their intended targets (ABCA1, HADHB, CPT1A, HADHA, GAPDH, and β-actin).
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“As shown in Fig. 6C, overexpression of miR-33 is associated with a 20% reduction of mitochondrial -oxidation.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“miR-33a and miR-33b are localized in corresponding introns of the human SREBP2 and SREBP1 genes, respectively (Fig. 1A and supplemental Fig. S3).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33a Is Produced from an Intron of the SREBP2 Gene and
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“the cell line transduced with the conditional miR-33a lentivirus shows strong reduction of ABCA1 levels upon treatment with doxycyclin (Fig. 4A, fifth to eighth lanes).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“we loaded cells with radioactively labeled cholesterol, and observed significantly reduced apoAI-dependent cholesterol export in the HepG2 liver cancer cell line (Fig. 3B) and THP1 monocytic leukemia cell line derived from macrophages (Fig. 4B).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“As shown in Fig. 6B, CROT mRNA levels were significantly reduced in cell lines overexpressing miR-33 to a degree that is similar to the reduction of ABCA1 and CPT1A”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We observed that miR-33a causes a marked decrease of ABCA1 protein levels (Fig. 3A, lanes 1 and 2) as assessed by immunoblot analysis.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
- Rests on an assumption: The antibodies used for Western blot analysis specifically detect their intended targets (ABCA1, HADHB, CPT1A, HADHA, GAPDH, and β-actin).
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Cotransfection of preMIR-33a significantly reduced the activity of the reporter construct containing the 3Ј UTR of ABCA1 (Fig. 2B).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- Probably not a substantial claim. 32
- It may state two separate claims as one. 30
- The quote only partly states this claim. 1
Every source the paper cites for this claim was checked and supports it.
In the paper
“However, SREBPs not only activate cholesterol synthesis but also fatty acid and phospholipid synthesis (2).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Supportedcites [2] Horton, 2002, J. Clin. Invest. source
The Abstract states that SREBPs activate genes involved in the synthesis of cholesterol, fatty acids, and phospholipids. The “SREBPs: two genes, three proteins” section also identifies an SREBP-1c target gene encoding an enzyme involved in phospholipid synthesis. Page numbers are not supplied for these passages. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“High levels of low density lipoprotein cholesterol are a major risk factor for the development of arteriosclerosis and death from cardiovascular causes (41).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Supportedcites [41] Nabel, 2003, N. Engl. J. Med. source
The section on elevated LDL cholesterol and coronary artery disease states that LDL is a causal agent in many forms of coronary heart disease. It also reports that people with markedly elevated LDL due to homozygous familial hypercholesterolemia develop severe coronary atherosclerosis and usually die from myocardial infarction. (LLM, conf=0.89)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Genes involved in its synthesis are coordinately up-regulated by the action of SREBP transcription factors (2).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > DISCUSSION
What the sources say
- Supportedcites [2] Horton, 2002, J. Clin. Invest. source
The “Function of individual SREBP isoforms in vivo” section reports that overexpressing SREBP-2 increases mRNAs encoding all cholesterol biosynthetic enzymes. The “SREBPs: two genes, three proteins” section also identifies SREBP-2 as preferentially activating cholesterol synthesis. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“It has been previously shown that the homologs of SREBPs do not respond to changes in cholesterol, but rather changes in palmitate and/or phospholipids (39,40).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
What the sources say
- Not checked — no full text of the sourcecites [39] Dobrosotskaya, 2002, Science source
- Partly supportedcites [40] Seegmiller, 2002, Dev. Cell sourceExperimental — accuracy not yet measured
The Results report that palmitate reduced nuclear dSREBP in Drosophila S2 cells, whereas a cholesterol-containing sterol mixture failed to do so. The Discussion proposes that palmitic acid or a lipid derived from it regulates this pathway, but does not establish phospholipids as the signal. The claim also generalizes beyond the Drosophila homolog studied here. (LLM, conf=0.86)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“It has been previously noted that cellular miR-33 levels are dependent on culture conditions and exogenous lipid supply (36).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
What the sources say
- Partly supportedcites [36] Tsuchiya, 2009, Nucleic Acids Res. sourceExperimental — accuracy not yet measured
The Results (Screening of miRNAs related with differentiation; page unavailable) report that miR-33a increased in T84 cells between culture days 0 and 7, supporting a limited link between its level and culture conditions. The paper does not report that exogenous lipid supply affects miR-33 levels; its cell-culture methods describe serum-containing medium, not a lipid-supply comparison. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This process seems to be essential for the formation of HDL particles because liver-and intestine-specific knockout mice for ABCA1 show strong reductions in HDL levels (45)(46)(47).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Not checked — no full text of the sourcecites [45] Brunham, 2009, Arterioscler. Thromb. Vasc. Biol. source
- Partly supportedcites [46] Singaraja, 2006, Arterioscler. Thromb. Vasc. Biol. sourceExperimental — accuracy not yet measured
The Abstract reports an 80% reduction in plasma HDL cholesterol in liver-specific ABCA1 knockout mice, supporting the liver-specific part of the claim. The paper does not report an intestine-specific knockout or its HDL levels. Its Discussion also says low HDL reflects increased catabolism as well as decreased synthesis, so the reduction alone does not establish a defect solely in particle formation. Page numbers are unavailable in our copy. (LLM, conf=0.88)
- Supportedcites [47] Brunham, 2006, J. Clin. Invest. source
The Introduction says ABCA1 promotes cholesterol and phospholipid efflux to apoA-I in the rate-controlling step of HDL particle formation. The Discussion describes hepatic ABCA1 as essential to HDL biogenesis and reports that intestinal ABCA1 deletion significantly reduces plasma HDL; the Results quantify the intestinal-knockout reduction at approximately 30%. (LLM, conf=0.92)
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In a process termed reverse cholesterol transport, peripheral tissues export their excess cholesterol to HDL using the cholesterol export pumps ABCA1 and ABCG1 (44).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Partly supportedcites [44] Yvan-Charvet, 2007, J. Clin. Invest. sourceExperimental — accuracy not yet measured
The Introduction (page not provided) describes HDL-mediated cholesterol removal from peripheral tissues and identifies ABCA1 and ABCG1 as cholesterol-efflux transporters. It distinguishes their acceptors, however: ABCA1 exports to lipid-poor apoA-1, not mature HDL particles, whereas ABCG1 exports to HDL. Thus the claim is too broad in saying both pumps export cholesterol to HDL. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Previous studies have shown that reduction of one or the other component in heterozygote knock-out mice leads to a concomitant reduction of the other subunit (31)(32)(33).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
What the sources say
- Supportedcites [31] Ibdah, 2001, J. Clin. Invest. source
The section “Generation and molecular characterization of MTP-deficient mice” reports that heterozygous Mtpa knockout mice had intermediate expression of both α and β subunits. This supports the claim for reduction of the α component in heterozygous mice accompanied by reduction of the β component. (LLM, conf=0.90)
- Partly supportedcites [32] Ibdah, 2005, Gastroenterology sourceExperimental — accuracy not yet measured
The Assessment of the Temporal Relationship section (page unavailable) reports lower hepatic MTP α-subunit expression in α-heterozygous mice than in wild-type mice. The Background & Aims section says α-null homozygotes lack both subunits, but the paper does not show a concomitant reduction of the β-subunit in heterozygotes or examine β-heterozygous knockouts. (LLM, conf=0.85)
- Partly supportedcites [33] Kao, 2006, Hum. Mol. Genet. sourceExperimental — accuracy not yet measured
The Discussion and Western blot and enzyme activity assay section report that both MTP subunits were reduced in affected mice with a mutation in the β-subunit. But the Identification of the mutated gene section identifies the affected mice as homozygous for a missense mutation, not heterozygous knockout mice; the paper therefore does not establish the claim for that genotype. (LLM, conf=0.89)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The reciprocal relationship also appears to be true in that increased gene dosage of ABCA1 increases plasma HDL levels and protects from arteriosclerosis in animal models of hyperlipidemia (48).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Partly supportedcites [48] Singaraja, 2001, J. Biol. Chem. sourceExperimental — accuracy not yet measured
The Results report significantly higher HDL-C in ABCA1 BAC transgenic mice than in control littermates, including when fed an atherogenic diet. The paper does not report an arteriosclerosis outcome or establish protection from arteriosclerosis in hyperlipidemic animal models; feeding an atherogenic diet does not by itself establish that protection. (LLM, conf=0.88)
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“D. melanogaster is a cholesterol auxotroph and activation of SREBP is regulated by reduced levels of palmitate and/or phospholipids.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Not checked — no full text of the sourcecites [39] Dobrosotskaya, 2002, Science source
- Partly supportedcites [40] Seegmiller, 2002, Dev. Cell sourceExperimental — accuracy not yet measured
The paper says insects require dietary sterols, supporting the description of D. melanogaster as a cholesterol auxotroph. The Results and Discussion show that added palmitate inhibits dSREBP processing in cultured Drosophila cells, but the Discussion says it is not clear whether palmitate itself or a more complex lipid, possibly a phospholipid, is responsible. It does not establish that reduced phospholipid levels activate SREBP. (LLM, conf=0.85)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“The mitochondrial trifunctional protein consists of an ␣ subunit (encoded by HADHA) and a  subunit (encoded by HADHB) (31).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
What the sources say
- Supportedcites [31] Ibdah, 2001, J. Clin. Invest. source
The Introduction states that mitochondrial trifunctional protein is a hetero-octamer of α and β subunits and explicitly identifies the genes coding for them as HADHA and HADHB, respectively. (LLM, conf=0.95)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This was observed both in mice that carry a hypomorphic allele of the HADHB gene and, notably, in mice heterozygote for a null mutation of the HADHA gene (encoding the ␣-subunit) (32,33).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Supportedcites [32] Ibdah, 2005, Gastroenterology source
The Background & Aims identifies the studied mice as heterozygous for an MTP α-subunit null allele, and Evaluation for Nonalcoholic Fatty Liver Disease reports hepatic steatosis in those mice. The finding was in aging mice; the paper reports no steatosis in young heterozygous mice. The separate HADHB example is not attributed to this source alone in the two-citation sentence. (LLM, conf=0.92)
- Supportedcites [33] Kao, 2006, Hum. Mol. Genet. source
The Identification of the mutated gene section identifies a homozygous Hadhb M404K mutation in the affected mice, and the Abstract reports hepatic steatosis in those mice. The enzyme activity results show reduced, rather than absent, activity, consistent with a hypomorphic allele. The HADHA heterozygote clause is accompanied by a separate citation and is not attributed to this paper. (LLM, conf=0.91)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Localization and sequence of this miRNA family is highly conserved down to insects and chordates, but not in worms.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33a Is Produced from an Intron of the SREBP2 Gene and
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Cotransfection of these constructs with preMIR-33 significantly reduced activation of constructs containing the wild type 3Ј UTR when compared with transfection with a preMIR control (Fig. 5, B, D, and F).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“With regard to their sequence, miR-33a and miR-33b differ only by two nucleotides outside the seed sequence (Fig. 1B).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33a Is Produced from an Intron of the SREBP2 Gene and
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Most species (including the mouse), however, only possess miR-33a in the SREBP2 gene and have lost the sequence of miR-33b within the SREBP1 gene (Fig. 1A and supplemental Fig. S3).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33a Is Produced from an Intron of the SREBP2 Gene and
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“overexpression of competitive antagonists of miR-33 action (i.e.miRNA sponges) in HepG2 cells led to an up-regulation of ABCA1 protein levels, which was accompanied by a significant increase in apoAI-dependent cellular cholesterol export (Fig. 3, C and D).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The miRNA sponges and antagomirs specifically inhibit miR-33 without off-target effects.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Several explanations seem possible to explain why we did not observe an increase in -oxidation and HADHB levels upon inhibition of miR-33.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The discovery that miR-33 inhibits ABCA1 expression and consequentially cellular cholesterol export suggests that one genetic locus increases synthesis and limits export of cholesterol through two distinct mechanisms (Fig. 8A).”
- Also stated in: § miR-33 in Cholesterol and Fatty Acid Metabolism · plain
“miR-33 reduces endogenous ABCA1 protein levels and modulates cellular cholesterol export in HepG2 cells.”
- Also stated in: § miR-33 in Cholesterol and Fatty Acid Metabolism · plain
“miR-33 reduces endogenous ABCA1 protein levels and modulates cellular cholesterol export in THP1 macrophages.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > DISCUSSION
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Also stated in: § miR-33 in Cholesterol and Fatty Acid Metabolism · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Inhibition of miR-33 with miRNA sponges or antisense oligonucleotides did not cause a reproducible increase in fatty acid -oxidation or alteration of HADHB and CPT1A protein levels in HepG2 cells (data not shown).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The miRNA sponges and antagomirs specifically inhibit miR-33 without off-target effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Site-directed mutagenesis of one or two of the predicted seed binding sites completely abolished this response (mutated nucleotides indicated by asterisks).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe quote only partly states this claim.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Culturing cells at high density and/or in lipid-free medium leads to an increase of miR-33 (supplemental Fig. S12A).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Notably, these two changes lead to a perfect complementarity of miR-33b with the CROT 3Ј UTR over a total of 18 nucleotides, which could allow miR-33b to induce Ago2-dependent cleavage of the CROT transcript (supplemental Fig. S8, B versus C).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“It should be noted that several prediction algorithms do not recognize CPT1A as a miR-33 target gene.This is due to the fact that these algorithms utilize a short 3Ј UTR generated from an alternative exon (supplemen- tal Fig. S9A).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When analyzing cellular extracts by TLC we observed a significant increase in cellular free fatty acid levels and triacylglycerides (Fig. 6D and supplemental Fig. S11).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 Inhibits Cellular Fatty Acid
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“miR-33 reduces endogenous ABCA1 protein levels and modulates cellular cholesterol export in HepG2 cells.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“miR-33 reduces endogenous ABCA1 protein levels and modulates cellular cholesterol export in THP1 macrophages.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“miR-33a localization within SREBP2 and sequences are evolutionary conserved.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In fact, there was a small, but not significant, trend for reduced miR-33 levels, as one might intuitively expect in a situation of hyperalimentation.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:plain· not yet calibratedn = 2Tests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“miR-33 reduces -oxidation and alters cellular fatty acid metabolism.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“CPT1A is the liver-specific isoform of the enzyme that converts acyl-CoA to acylcarnitine and thereby allows fatty acids to enter the mitochondrion where fatty acid -oxidation takes place (27).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [27] Bonnefont, 2004, Mol. Aspects Med. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“ABCA1 acts as a cellular cholesterol export pump.Although there are a number of cholesterol efflux pumps, ABCA1 has the unique capability to export cholesterol to lipid-free apolipoprotein AI (apoAI) and is therefore involved in the initial step of high-density lipoprotein particle formation in liver, as well as reverse cholesterol transport (26).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [26] Tall, 2008, Cell Metab. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The genetic locus encoding SREBP2 and miR-33 therefore contains a protein that increases lipid synthesis and a miRNA that prevents export and degradation of newly synthesized lipids.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“CROT, sometimes abbreviated COT, is a peroxisomal enzyme that couples short chain fatty acids to carnitine and thereby allows their entry in the mitochondrial matrix.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [29] Wanders, 2010, Biochim. Biophys. Acta source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Although not strictly an enzyme of the -oxidation, the activity of CPT1A is rate-limiting for oxidation, and is the most highly regulated element in this metabolic pathway (28).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [28] Saggerson, 2008, Annu. Rev. Nutr. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Taken together, our data suggest that endogenous miR-33 targets and represses translation of ABCA1, and reduces cellular cholesterol export.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“It has recently been noted that cancer cell lines and proliferative cells often express transcripts with shorter 3Ј UTRs (51).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [51] Sandberg, 2008, Science source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Loss-of-function alleles of ABCA1 are associated with a decrease in HDL levels and might be associated with an increase in cardiovascular mortality (42,49).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Given its preventive effect in mice, increasing ABCA1 protein levels by inhibiting miR-33 might therefore prove useful in the prevention of cardiovascular diseases.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“Inactivating mutations in ABCA1 lead to the development of Tangier disease, which is characterized by the absence of HDL and the accumulation of cholesterol in peripheral tissues (42).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
- Not checked — no full text of the sourcecites [42] Brunham, 2008, JAMA source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Although CROT is localized to the peroxisomes, it serves to transfer remnants from peroxisomal -oxidation to the mitochondria and therefore fuels mitochondria with fatty acids independently of CPT1A (29).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [29] Wanders, 2010, Biochim. Biophys. Acta source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When decreases in cellular cholesterol levels trigger the activation of SREBP transcription factors, the presence of miR-33 prevents cholesterol from leaving the cell by suppressing expression of ABCA1, thus allowing cellular cholesterol levels to be restored (Fig. 8A).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > DISCUSSION
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“On the other hand, elevated levels of high density lipoprotein cholesterol reduces the risk of arteriosclerosis (42,43).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The gene HADHB encodes for the -subunit of the mitochondrial trifunctional protein that carries out the last three steps of -oxidation (30).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [30] Eaton, 2000, Biochem. Soc. Trans. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Peroxisomal -oxidation is limited to the degradation of long-and medium-chain fatty acids as it is not able to oxidize short chain fatty acids (29).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [29] Wanders, 2010, Biochim. Biophys. Acta source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Agents that alter HDL cholesterol levels therefore carry the potential to reduce cardiovascular diseases.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > JOURNAL OF BIOLOGICAL CHEMISTRY 33657
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Presently, non-alcoholic fatty liver disease (NAFLD) is by far the most common liver ailment (53).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [53] Angulo, 2002, N. Engl. J. Med. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Likewise, altering the levels of HADHB might change the potential maximum flux through -oxidation, but might have little influence under most conditions where fatty acid supply in the mitochondria is rate-limiting for -oxidation.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Protein amounts of SREBPs therefore represent the maximum potential to respond to changes in lipid levels.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Interfering with miR-33 function in vivo therefore not only holds promise in increasing HDL cholesterol levels but may also prove beneficial for treatment of NAFLD and NASH.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“With the increasing prevalence of obesity, it affects 10 -25% of the general population and up to 75% of obese type II diabetic patients (54).”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [54] Marchesini, 2008, J. Clin. Endocrinol. Metab. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“A recent study of Cabellero and co-workers (55) suggests that SREBP2 transcript levels in NAFLD and NASH are elevated 3-and 7-fold, respectively.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
What the sources say
- Not checked — no full text of the sourcecites [55] Caballero, 2009, J. Hepatol. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The relevance of targeting HADHB is not quite as apparent, although reduced HADHB concentrations might help maintain adequate intermediary product levels in a situation where the enzyme that supplies the substrates for -oxidation (CPT1A and CROT) is inhibited.”
§ Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation * □ S > miR-33 in Cholesterol and Fatty Acid Metabolism
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
The paper relies on this without support.
The 500-bp genomic region surrounding miR-33a used in lentiviral vectors specifically expresses miR-33a without affecting other genes or small RNAs.
“we transduced HepG2 cells with a lentiviral expression vector constitutively driving expression of a 500-bp genomic region surrounding the miR-33a sequence.”
The paper relies on this without support.
The antibodies used for Western blot analysis specifically detect their intended targets (ABCA1, HADHB, CPT1A, HADHA, GAPDH, and β-actin).
“Antibodies were used at the following dilutions: ABCA1 at 1:1,000 (AB.H10, Santa Cruz Biotechnologies), HADHB at 1:1,000 (ARP48133, Aviva Systems Biology, San Diego, CA), HADHA at 1:1,000 (HPA015536, Sigma), CPT1 1:1000 (Proteintech, Manchester, UK), GAPDH at 1:2,000 (6C5, Pierce-ThermoFisher), and -actin at 1:10,000 (AC-40, Sigma).”
The paper relies on this without support.
The miRNA sponges and antagomirs specifically inhibit miR-33 without off-target effects.
“miR-33 antagomir denotes a 1:1 mixture of miR-33a and miR-33b antagomir.”
The paper relies on this without support.
D. melanogaster and other Drosophilids are cholesterol auxotrophs (cannot synthesize cholesterol).
“Notably, miR-33 is highly conserved in D. melanogaster (and other Drosophilids), which are auxotrophs for cholesterol, i.e. they cannot synthesize cholesterol.”
The paper relies on this without support.
SREBPs of higher organisms help to coordinately induce genes involved in cholesterol, fatty acid, and phospholipid synthesis.
“As mentioned above, SREBPs of higher organisms help to coordinately induce genes involved in cholesterol, fatty acid, and phospholipid synthesis.”
The paper relies on this without support.
Activation of SREBPs stimulates transcription of several genes involved in fatty acid synthesis.
“Activation of SREBPs stimulates transcription of several genes involved in fatty acid synthesis.”
The paper relies on this without support.
CPT1A is the rate-limiting and most highly regulated step in β-oxidation.
“As mentioned before, CPT1A is the rate-limiting and most highly regulated step in -oxidation.”
The paper relies on this without support.
CROT and CPT1A are enzymes that couple fatty acids to carnitine.
“CROT and CPT1A are enzymes that couple fatty acids to carnitine.”
The paper relies on this without support.
The protein product of the HADHB transcript forms the β-subunit of the mitochondrial trifunctional protein, which carries out three steps of β-oxidation.
“The protein product of the HADHB transcript forms the -subunit of the mitochondrial trifunctional protein, which carries out three steps of -oxidation.”
The paper relies on this without support.
No single mouse model or feeding regimen reliably reproduces the features of NAFLD and NASH.
“Unfortunately, no single mouse model or feeding regimen reliably reproduces the features of NAFLD and NASH.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“miR-33a and miR-33b help prevent further loss of lipids by targeting genes involved in cholesterol trafficking and efflux”
From Genetic dissection of the impact of miR-33a and miR-33b during the progression of atherosclerosis (2017) · cites this paper as Gerin et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In miR-33a knockout mice or when miR-33a is suppressed by synthetic nucleic acids such as antagomirs, the expression of ABCA1 in macrophages and the liver is increased 11 - 15) .”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [15]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Two miR-33 genes are present in humans: miR-33b, which is present in intron 17 of the Srebp-1 gene on chromosome 17, and miR-33a, which is located in intron 16 of the Srebp-2 gene on chromosome 22.”
From miR-33a/b contribute to the regulation of fatty acid metabolism and insulin signaling (2011) · cites this paper as [11]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In mice, however, there is only one miR-33 gene, which is conserved with human miR-33a and located within intron 15 of the mouse Srebp-2 gene.”
From miR-33a/b contribute to the regulation of fatty acid metabolism and insulin signaling (2011) · cites this paper as [11]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The most well-known target gene of miR-33a/b is ATP-binding cassette subfamily A member 1 (ABCA1).”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [15]
The cited source says what the claim attributes to it.
In the citing paper
“MiR-33 suppresses genes involved in mitochondrial β-oxidation, such as carnitine palmitoyltransferase 1A (CPT1A), hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit b (HADHB), and carnitine O-octanoyltransferase (CROT) 15 , 17 , 34 , 35) .”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [15]
The cited source says what the claim attributes to it.
In the citing paper
“We and others provided identification of a highly conserved miRNA family, miR-33, within the intronic sequences of the Srebp genes in organisms ranging from Drosophila to humans (11–14).”
From miR-33a/b contribute to the regulation of fatty acid metabolism and insulin signaling (2011) · cites this paper as [11]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Two articles are cited with a three-reference range
MinorThe addendum says two articles were presented online but cites references 56-58, a range containing three separately listed articles.
“two articles were presented online describing the effect of miR-33 on ABCA1 and cholesterol metabolism (56 -58).”
“58. Marquart, T. J., Allen, R. M., Ory, D. S., and Balda ´n, A. (2010) Proc. Natl. Acad. Sci. U.S.A. 107, 12228 -12232”
Cholesterol-export error bars are described as both SD and SE
MinorThe cholesterol-export methods say the displayed values are means ± SD, whereas the Figure 3 legend describes the cholesterol-export results as means ± SE. These are different measures of variability.
“Experiments were performed using 5 to 8 replicates per experimental condition and values shown represent mean Ϯ S.D.”
“Values represent mean Ϯ S.E. of 6 replicates.”
Citations
Cites
A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES
Folch, J., Lees, M., & Stanley, G. H. S. (1957) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)64849-5 · Cited by 65,189
MicroRNAs: Target Recognition and Regulatory Functions
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Nonalcoholic Fatty Liver Disease
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SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver
Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15593 · Cited by 4,794
Combinatorial microRNA target predictions
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SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver
Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215593 · Cited by 4,092
Silencing of microRNAs in vivo with ‘antagomirs’
Krützfeldt, J., Rajewsky, N., Braich, R., Rajeev, K. G., Tuschl, T., Manoharan, M., & Stoffel, M. (2005) · Nature · doi:10.1038/nature04303 · Cited by 3,949
MicroRNA Targeting Specificity in Mammals: Determinants beyond Seed Pairing
Grimson, A., Farh, K. K.-H., Johnston, W. K., Garrett-Engele, P., Lim, L. P., & Bartel, D. P. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.06.017 · Cited by 3,766
The impact of microRNAs on protein output
Baek, D., Villén, J., Shin, C., Camargo, F. D., Gygi, S. P., & Bartel, D. P. (2008) · Nature · doi:10.1038/nature07242 · Cited by 3,592
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Items 101–200 of 383
SREBP-1c/MicroRNA 33b Genomic Loci Control Adipocyte Differentiation
Price, N. L., Holtrup, B., Kwei, S. L., Wabitsch, M., Rodeheffer, M. S., Bianchini, L., Suárez, Y., & Fernandez-Hernando, C. F. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00745-15 · Cited by 61
Canfrán‐Duque, A., Ramírez, C. M., Goedeke, L., Lin, C., & Fernandez-Hernando, C. F. (2014) · Cardiovascular Research · doi:10.1093/cvr/cvu140 · Cited by 59
Post-transcriptional Regulation of PCSK9 by miR-191, miR-222, and miR-224
Naeli, P., Mirzadeh Azad, F., Malakootian, M., Seidah, N. G., & Mowla, S. J. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00189 · Cited by 58
“Cholesterol synthesis rate was also decreased upon miR-122 inhibition (Esau et al., 2006). miR-33 is one of the well-studied miRNAs related to lipid and cholesterol metabolism. miR-33 is encoded within the sterol-regulatory element-binding factor-2 (SREBP2), a transcription factor that regulates lipid metabolism and r…”
The investigations of genetic determinants of the metabolic syndrome
Dizaji, B. F. (2018) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2018.04.009 · Cited by 68
Wang, H., Luo, J., Zhang, T., Tian, H., Ma, Y., Xu, H., Yao, D., & Loor, J. J. (2016) · RNA Biology · doi:10.1080/15476286.2016.1164365 · Cited by 58
“MiR-33a/b act in concert with SREBF2 to control cholesterol homeostasis.(14,17)”
BackgroundmicroRNAs in lipoprotein and lipid metabolism: from biological function to clinical application
Desgagné, V., Bouchard, L., & Guérin, R. (2016) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2016-0575 · Cited by 57
Deciphering Non-coding RNAs in Cardiovascular Health and Disease
Das, A., Samidurai, A., & Salloum, F. N. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00073 · Cited by 56
Self-citationEyeballing cholesterol efflux and macrophage function in disease pathogenesis
Sène, A., & Apte, R. S. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.10.007 · Cited by 56
Efferocytosis and Atherosclerosis: Regulation of Phagocyte Function by MicroRNAs
Tajbakhsh, A., Bianconi, V., Pirro, M., Hayat, S. M. G., Johnston, T. P., & Sahebkar, A. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.07.006 · Cited by 57
Key events in cancer: Dysregulation of SREBPs
Li, Y., Wu, S., Zhao, X., Hao, S., Li, F., Wang, Y.-X., Liu, B., Zhang, D., Wang, Y., & Zhou, H. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1130747 · Cited by 62
“, 2010) but also works with miR-33b and their SREBP host gene products to regulate intracellular fatty acid and lipid levels (Gerin et al., 2010; Dávalos et al., 2011).”
BackgroundRelevance of microRNA in metabolic diseases
Price, N. L., Ramírez, C. M., & Fernandez-Hernando, C. F. (2014) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408363.2014.937522 · Cited by 55
Systematic analysis of the regulatory functions of microRNAs in chicken hepatic lipid metabolism
Li, H., Ma, Z., Jia, L., Li, Y., Xu, C., Wang, T., Han, R., Jiang, R., Li, Z., Sun, G., et al. (2016) · Scientific Reports · doi:10.1038/srep31766 · Cited by 56
MicroRNAs in lipid metabolism and atherosclerosis
Giral, H., Kratzer, A., & Landmesser, U. (2016) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2016.11.010 · Cited by 55
Posttranscriptional regulation of lipid metabolism by non-coding RNAs and RNA binding proteins
Singh, A. K., Aryal, B. K., Zhang, X., Fan, Y., Price, N. L., Suárez, Y., & Fernandez-Hernando, C. F. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.11.026 · Cited by 55
“Among the miRNAs involved in regulation of HDL-C metabolism, miR-33 is deemed to be one of the most important, due to its ability to regulate numerous key functions including cholesterol efflux, transport and uptake; HDL biogenesis; bile acid synthesis and secretion; and fatty acid degradation [40, 53-58].”
BackgroundBenraiss, A., Mariani, J. N., Osipovitch, M., Cornwell, A., Windrem, M. S., Villanueva, C. B., Chandler-Militello, D., & Goldman, S. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109308 · Cited by 52
Zhang, P., Huang, C., Fu, C., Tian, Y., Hu, Y., Wang, B., Strasner, A., Song, Y., & Song, E. (2015) · Oncotarget · doi:10.18632/oncotarget.3383 · Cited by 54
“miR-33 also binds to 3’UTR of carnitine O-octaniltransferase (CROT), Carnitine palmitoyltransferase 1A (CPT1a) and hydroxyacylCoA-dehydrogenase (HADHB) to regulate fatty acid metabolism [47].”
Tarling, E. J., & Edwards, P. A. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2011.07.011 · Cited by 54
Antipsychotics Promote Metabolic Disorders Disrupting Cellular Lipid Metabolism and Trafficking
Vantaggiato, C., Panzeri, E., Citterio, A., Orso, G., & Pozzi, M. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.01.003 · Cited by 56
Complexity of microRNA function and the role of isomiRs in lipid homeostasis
Vickers, K. C., Sethupathy, P., Baran‐Gale, J., & Remaley, A. T. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r034801 · Cited by 52
Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression
Link, J. C., Hasin-Brumshtein, Y., Cantor, R. M., Chen, X., Arnold, A. P., Lusis, A. J., & Reue, K. (2017) · BMC Genomics · doi:10.1186/s12864-017-3484-1 · Cited by 52
“For example, miR-33a and miR33b, which are embedded within genes for sterol regulatory element-binding proteins Srebf2 and Srebf1, respectively, have key roles in the modulation of cholesterol homeostasis [14, 15].”
BackgroundNovák, J., Vašků, J. B., Kára, T., & Novák, M. (2014) · Mediators of Inflammation · doi:10.1155/2014/275867 · Cited by 52
“OxLDL molecules may be”
BackgroundExosomes in Cardiovascular Disease: From Mechanism to Therapeutic Target
Reiss, A. B., Ahmed, S., Johnson, M., Saeedullah, U., & Leon, J. D. (2023) · Metabolites · doi:10.3390/metabo13040479 · Cited by 54
Dávalos, A., & Fernandez-Hernando, C. F. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.02.005 · Cited by 52
Gracia, A., Miranda, J., Fernández‐Quintela, A., Eseberri, I., Garcia-Lacarte, M., Milagro, F. I., Martínez, J. A., Aguirre, L., & Portillo, M. P. (2016) · Food & Function · doi:10.1039/c5fo01090j · Cited by 50
Horie, T., Nishino, T., Baba, O., Kuwabara, Y., Nakao, T., Nishiga, M., Usami, S., Izuhara, M., Nakazeki, F., Ide, Y., et al. (2014) · Scientific Reports · doi:10.1038/srep05312 · Cited by 49
Price, N. L., Zhang, X., Fernández-Tussy, P., Singh, A. K., Burnap, S. A., Rotllan, N., Goedeke, L., Sun, J., Canfrán-Duque, A., Aryal, B., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2006478118 · Cited by 50
microRNAs: A connection between cholesterol metabolism and neurodegeneration
Goedeke, L., & Fernandez-Hernando, C. F. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.05.034 · Cited by 49
“2013 Rayner KJ, Esau CC, Hussain FN, McDaniel AL, Marshall SM, van Gils JM, Ray TD, Sheedy FJ, Goedeke L, Liu X, Khatsenko OG, Kaimal V, Lees CJ, Fernandez-Hernando C, Fisher EA, Temel RE, Moore KJ. Inhibition of miR-33a/b in non-human primates raises plasma HDL and lowers VLDL triglycerides.”
BackgroundInfluentialLi, H., Xi, Q., Xiong, Y., Liu, X., Cheng, X. L., Shu, G., Wang, S., Wang, L., Gao, P., Zhu, X., et al. (2012) · Animal Genetics · doi:10.1111/j.1365-2052.2012.02332.x · Cited by 48
“…have consistently indicated that miRNAs are involved in adipocyte differentiation and fat metabolism, including reducing fatty acid degradation (Gerin et al. 2010), promoting the differentiation of preadipocytes into mature adipocytes (Esau et al. 2004; Li et al. 2011) and impairing adipocyte…”
BackgroundFisetin protects against hepatosteatosis in mice by inhibiting miR-378
Jeon, T., Park, J. W., Ahn, J., Jung, C. H., & Ha, T. Y. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201300071 · Cited by 47
Microtargeting cancer metabolism: opening new therapeutic windows based on lipid metabolism
de Cedrón, M. G., & de Molina, A. R. (2016) · Journal of Lipid Research · doi:10.1194/jlr.r061812 · Cited by 49
microRNAs and cancer metabolism reprogramming: the paradigm of metformin.
Pulito, C., Donzelli, S., Muti, P. C., Puzzo, L., Strano, S., & Blandino, G. (2014) · PubMed Central · doi:10.3978/j.issn.2305-5839.2014.06.03 · Cited by 49
“In addition, this condition induced fatty acid degradation in human liver cells, through the lack of modulation in the expression of genes involved in the oxidation of fatty acid (77,80).”
BackgroundGebreyesus, G., Buitenhuis, B., Poulsen, N. A., Visker, M. H. P. W., Zhang, Q., van Valenberg, H. J. F., Sun, D., & Bovenhuis, H. (2019) · BMC Genomics · doi:10.1186/s12864-019-5573-9 · Cited by 47
Therapeutic Potential of Modulating microRNAs in Atherosclerotic Vascular Disease
Araldi, E., Chamorro-Jorganes, A., Solingen, C. V., Fernandez-Hernando, C. F., & Suárez, Y. (2015) · Current Vascular Pharmacology · doi:10.2174/15701611113119990012 · Cited by 47
Steen, V. M., Skrede, S., Polushina, T. V., López, M., Andreassen, O. A., Fernø, J., & Hellard, S. L. (2016) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.07.011 · Cited by 48
Zhu, T., Corraze, G., Plagnes-Juan, E., Quillet, E., Dupont-Nivet, M., & Skiba-Cassy, S. (2018) · American Journal of Physiology. Regulatory Integrative and Comparative Physiology · doi:10.1152/ajpregu.00179.2017 · Cited by 45
miRNA regulation of LDL-cholesterol metabolism
Goedeke, L., Wagschal, A., Fernández-Hernando, C., & Näär, A. M. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2016.03.007 · Cited by 39
Gerin, I., Noël, G., Bolsée, J., Haumont, O., SCHAFTINGEN, E. V., & Bommer, G. T. (2014) · Biochemical Journal · doi:10.1042/bj20130841 · Cited by 48
Self-citationThe role of DNA methylation in dyslipidaemia: A systematic review
Braun, K. V. E., Voortman, T., Dhana, K., Troup, J., Bramer, W. M., Troup, J., Chowdhury, R., Dehghan, A., Muka, T., & Franco, O. H. (2016) · Progress in Lipid Research · doi:10.1016/j.plipres.2016.10.002 · Cited by 45
HADHB, a fatty acid beta-oxidation enzyme, is a potential prognostic predictor in malignant lymphoma
Sekine, Y., Yamamoto, K., Kurata, M., Honda, A., Onishi, I., Kinowaki, Y., Kawade, G., Watabe, S., Nomura, S., Fukuda, S., et al. (2021) · Pathology · doi:10.1016/j.pathol.2021.06.119 · Cited by 47
The Regulation of Reverse Cholesterol Transport and Cellular Cholesterol Homeostasis by MicroRNAs
DiMarco, D. M., & Fernández, M. (2015) · Biology · doi:10.3390/biology4030494 · Cited by 33
Xu, F., Wang, X., Feng, Y., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104371 · Cited by 44
“The PLOS ONE | www.plosone.org 4 August 2014 | Volume 9 | Issue 8 | e104371 products of the SREBF family are post-translationally activated in situations with reduced lipid abundance and are responsible for cholesterol, fatty acid, and phospholipid synthesis, while miR-33 reduces the degradation of these materials by…”
BackgroundXu, J., Hu, G., Lu, M. H., Xiong, Y., Li, Q., Chang, C. C. Y., Song, B., Chang, T., & Li, B.-L. (2013) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmt096 · Cited by 43
miRNA and cholesterol homeostasis
Jeon, T.-I., & Osborne, T. F. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2016.01.005 · Cited by 43
Gadde, S., & Rayner, K. J. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.307481 · Cited by 44
Han, Q., Su, D., Shi, C., Liu, P., Wang, Y., Zhu, B., & Xia, X. (2020) · Food & Function · doi:10.1039/c9fo02471a · Cited by 44
MicroRNA regulation of cholesterol metabolism
Citrin, K. M., Fernandez-Hernando, C. F., & Suárez, Y. (2021) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14566 · Cited by 45
Regulation of cholesterol biosynthesis and lipid metabolism: A microRNA management perspective
Bhattarai, A., Likos, E., Weyman, C. M., & Shukla, G. C. (2021) · Steroids · doi:10.1016/j.steroids.2021.108878 · Cited by 44
MicroRNAs in Cardiometabolic Disease
Najafi-Shoushtari, S. H. (2011) · Current Atherosclerosis Reports · doi:10.1007/s11883-011-0179-y · Cited by 41
Christian, P., & Su, Q. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00194.2014 · Cited by 42
“FASN FA synthesis 1 Plasma TG ACC2 FA synthesis 1 Lipid synthesis SCD1 FA synthesis 2 FA oxidation ACLY FA synthesis AMPK FA oxidation miR-33a/b HADHB FA oxidation 2 FA oxidation (18, 26, 33, 61, 65)”
BackgroundInfluentialDong, J., Liang, Y., Zhang, J., Wu, L., Wang, S., Hua, Q., & Yan, Y.-X. (2016) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.35923 · Cited by 41
Ortega, R., Liu, B., & Persaud, S. J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310777 · Cited by 45
“For this purpose, different strategies, including genetic miR-33 ablation [17,35] and pharmacological modulation of miR-33 expression using lentivirus or antisense nucleotides [27,36], have been pursued, but further investigations are needed to clarify the beneficial effects of targeting miR-33 on specific organs and…”
BackgroundHDL—A molecule with a multi-faceted role in coronary artery disease
Arora, S., Patra, S. K., & Saini, R. (2015) · Clinica Chimica Acta · doi:10.1016/j.cca.2015.10.021 · Cited by 40
MicroRNAs and lipoproteins: a connection beyond atherosclerosis?
Norata, G., Sala, F., Catapano, A., & Fernández-Hernando, C. (2012) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2012.11.019 · Cited by 43
“Over-expression of miR-33 in hepatic cells significantly reduces the degradation of fatty acids leading to an accumulation of neutral lipids [8, 28].”
BackgroundInfluentialmiR-33a is a tumor suppressor microRNA that is decreased in prostate cancer
Karatas, O., Wang, J.-H., Shao, L.-J., Ozen, M., Zhang, Y.-Q., Creighton, C., & Ittmann, M. (2017) · OncoTarget · doi:10.18632/oncotarget.19521 · Cited by 40
“Similar results were seen with the correlation between SREBF2 and HADHA, which have been shown to be downregulated in parallel to a well-known miR-33a target, HADHB [26] (Figure 7D).”
BackgroundResultInfluentialControl of very low-density lipoprotein secretion by N-ethylmaleimide-sensitive factor and miR-33
Allen, R. M., Marquart, T. J., Jesse, J. J., & Baldán, Á. (2014) · Circulation Research · doi:10.1161/circresaha.115.303100 · Cited by 38
Villacorte-Tabelin, M., Delmarcelle, A.-S., Lernoux, M., Bouquet, M., Lemoine, P., Bolsée, J., Umans, L., Lopes, S. M. C. D. S., Smissen, P. V. D., Sasaki, T., et al. (2016) · Development · doi:10.1242/dev.134171 · Cited by 38
“Lentiviral infection Lentiviral constructs driving expression of shRNA against laminin α1 were generated as described previously (Gerin et al., 2010).”
MethodSelf-citationMicroRNA-33 in atherosclerosis etiology and pathophysiology.
Chen, W.-J., Zhang, M., Zhao, G.-J., Fu, Y., Zhang, D.-W., Zhu, H.-B., & Tang, C.-K. (2013) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2012.11.025 · Cited by 41
“SLC25A25 Sapiens solute carrier family 25 [16,33,56]”
BackgroundInfluentialJia, L., Song, N., Yang, G.-L., Ma, Y.-X., Li, X.-T., Lu, R., Cao, H., Zhang, N., Zhu, M.-L., Wang, J., et al. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.5133 · Cited by 36
“In the current study, miR-33a expression was observed to be upregulated, whilst the expression levels of ABCA1 and ABCG1 were reduced in the liver tissues of HLP rats, which further supports that ABCA1 and ABCG1 are the miR-33a target genes.”
InfluentialmiR‐33 in cardiometabolic diseases: lessons learned from novel animal models and approaches
Price, N. L., Goedeke, L., Suárez, Y., & Fernández‐Hernando, C. (2021) · EMBO Molecular Medicine · doi:10.15252/emmm.202012606 · Cited by 36
“In addition to controlling fatty acid metabolism, miR-33 also regulates insulin signaling and glucose metabolism (Gerin et al, 2010; Davalos et al, 2011; Ramirez et al, 2013).”
BackgroundInfluentialWang, Y., Zhou, X., Shan, B., Han, J., Wang, F., Fan, X., Lv, Y., Chang, L., & Liu, W. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4296 · Cited by 36
“…cycle arrest in G 1 phase. miRNAs have roles of post-transcriptional regulation by inhibiting the expression of their target genes. miR-33a regulates cholesterol levels by targeting Abca1, Abcg1 and Npc1 (9-11) as well as fatty acid metabolism by targeting Ampk, Cpt1a, Crot, Hadhb and Sirt6 (8,12).”
CryomiRs: Towards the identification of a cold-associated family of microRNAs
Lyons, P. J., Lang-Ouellette, D., & Morin, P. (2013) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2013.10.001 · Cited by 36
Posttranscriptional Regulation of ATP-Binding Cassette Transporter A1 in Lipid Metabolism
Lv, Y.-C., Yin, K., Fu, Y., Zhang, D., Chen, W., & Tang, C. (2013) · DNA and Cell Biology · doi:10.1089/dna.2012.1940 · Cited by 36
“MiR-33a and miR-33b differ by only two nucleotides outside the seed sequence (Gerin et al ., 2010).”
Mitochondrial miRNAs in diabetes: just the tip of the iceberg
Baradan, R., Hollander, J. M., & Das, S. (2017) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2016-0580 · Cited by 36
Ren, J., Tian, W., Jiang, K., et al. (2021) · BMC Genomics · doi:10.1186/s12864-021-07679-y · Cited by 36
“Several other differentially expressed known miRNAs participate in lipid metabolism, including miR33 [23], miR-10b [24], and miR-30e [25].”
BackgroundNovel concepts in HDL pharmacology
Remaley, A. T., Norata, G. D., & Catapano, A. L. (2014) · Cardiovascular Research · doi:10.1093/cvr/cvu141 · Cited by 36
MicroRNA-33a/b in Lipid Metabolism
Ono, K., Horie, T., Nishino, T., Baba, O., Kuwabara, Y., Yokode, M., Kita, T., & Kimura, T. (2015) · Circulation Journal · doi:10.1253/circj.cj-14-1252 · Cited by 34
MicroRNA-221 may be involved in lipid metabolism in mammary epithelial cells
Chu, M., Zhao, Y. M., Yu, S., Hao, Y., Zhang, P., Feng, Y., Zhang, H., Ma, D., Liu, J., Cheng, M. Y., et al. (2018) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2018.02.014 · Cited by 34
Are microRNAs the Molecular Link Between Metabolic Syndrome and Alzheimer’s Disease?
Codocedo, J. F., Ríos, J. A., Godoy, J. A., & Inestrosa, N. C. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9201-7 · Cited by 34
“cholesterol, primarily through the transcriptional repression of the ATP-binding cassette transporters 1 (ABCA1) [99], which mediates an essential step in the formation of high-density”
BackgroundThe Complexity of Thyroid Transcription Factor 1 with Both Pro- and Anti-oncogenic Activities
Mu, D. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.r113.491647 · Cited by 33
Post-transcriptional regulation in metabolic diseases
Kim, W., & Lee, E. K. (2012) · RNA Biology · doi:10.4161/rna.20091 · Cited by 33
Wang, J., Lu, R., Sun, J.-J., Xie, D., Yang, F., & Nie, G.-X. (2016) · Aquaculture Research · doi:10.1111/are.13228 · Cited by 33
The salient role of microRNAs in atherogenesis
Donaldson, C. J., Lao, K. H., & Zeng, L. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.08.004 · Cited by 32
Wan, N., Xu, Z., Chi, Q.-R., Hu, X.-Y., Pan, T., Liu, T., & Li, S. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28050 · Cited by 33
“…only is it involved in the regulation of lipid metabolism, fatty acid oxidation, phospholipid and triglyceride metabolism, and bile acid metabolism (Gerin et al., 2010; Ho, Chang, Chuang, & Wei, 2011; Rayner et al., 2011a), but it also participates in the regulation of other signaling pathways…”
Background‘Micro‐managers’ of hepatic lipid metabolism and NAFLD
Liu, W., Cao, H., Yan, J., Huang, R., & Ying, H. (2015) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1295 · Cited by 33
Expression of miR-33 from an SREBF2 Intron Targets the FTO Gene in the Chicken
Shao, F., Wang, X., Yu, J., Jiang, H., Zhu, B., & Gu, Z. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091236 · Cited by 33
“Research by multiple groups has shown that miR-33 analogs regulate cholesterol and fatty acid metabolism in mammalian systems, corresponding with the function of its host gene [10,11].”
BackgroundSocial status affects lipid metabolism in rainbow trout,Oncorhynchus mykiss
Kostyniuk, D. J., Culbert, B. M., Mennigen, J. A., & Gilmour, K. M. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00402.2017 · Cited by 32
“Functionally, several studies in mammalian models provide evidence for a role of srebp2 intronencoded miRNA-33 in stimulating hepatic cholesterol abundance by limiting cholesterol efflux via abc transport proteins (32, 36, 41, 65, 72), thus augmenting the principal role of its srebp2 host gene as a key transcription f…”
BackgroundMicroRNAs as Regulators of Cancer Cell Energy Metabolism
Natarajaseenivasan, S. M., Velusamy, P., Mercy, C. S. A., Langford, D., Natarajaseenivasan, K., & Shanmughapriya, S. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12081329 · Cited by 35
“The miR-33a/b-encoding genes are present within the intron sequences of human SREBF genes, and miR-33a/b is known to regulate the expression of ATP-binding cassette transporter ABCA1 [164,165].”
BackgroundHuang, J., Li, Y., Ma, F., et al. (2018) · Gene · doi:10.1016/j.gene.2018.09.012 · Cited by 32
MicroRNA-126 participates in lipid metabolism in mammary epithelial cells
Chu, M., Zhao, Y. M., Feng, Y., Zhang, H., Liu, J., Cheng, M. Y., Li, L., Shen, W., Cao, H., Li, Q., et al. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.05.039 · Cited by 32
“miR-33a and miR-33b regulate cholesterol metabolism (Rayner et al., 2011; Marquart et al., 2010; Gerin et al., 2010; Horie et al., 2010; NajafiShoushtari et al., 2010); miR-27b binds to the 30-UTR of several lipid-associated genes: heparan sulfate N-deacetylase/N-sulfotransferase 1 (NDST1), angiopoietin-like 3 (ANGPTL…”
BackgroundMacrophage MicroRNAs as Therapeutic Targets for Atherosclerosis, Metabolic Syndrome, and Cancer
Wei, Y., Zhu, M., & Schober, A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061756 · Cited by 32
“carnitine palmitoyltransferase 1A, hydroxyacyl-CoA dehydrogenase, Sirtuin 6, and AMP kinase subunit-α [45,46].”
BackgroundRNAs with multiple personalities
Maute, R. L., Dalla‐Favera, R., & Basso, K. (2013) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1193 · Cited by 30
Non-Coding RNAs and Lipid Metabolism
Smolle, E., & Haybaeck, J. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150813494 · Cited by 32
“The expression of several miR-33b target genes, all involved in fatty acid oxidation, was also increased, namely CROT, CPT1A, HADHB and PRKAA1.”
BackgroundGrowth Hormone-Regulated mRNAs and miRNAs in Chicken Hepatocytes
Wang, X.-G., Yang, L., Wang, H.-J., Shao, F., Yu, J.-F., Jiang, H.-L., Han, Y., Gong, D., & Gu, Z. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112896 · Cited by 32
“miR-33 is another miRNA involved in liver metabolism: it regulates cholesterol efflux and high-density lipoprotein metabolism by targeting ATP-binding cassette, subfamily A (ABC1), member 1 and ATP-binding cassette, sub-family G (WHITE), member 1 [19], and it reduces fatty acid degradation by targeting multiple genes…”
BackgroundChen, W., Huang, Q.-Y., Wang, Z., Zhuang, X., Lin, S., & Shi, Q. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.918805 · Cited by 30
The interplay between microRNAs and Twist1 transcription factor: a systematic review
Khanbabaei, H., Teimoori, A., & Mohammadi, M. (2016) · Tumor Biology · doi:10.1007/s13277-016-4960-y · Cited by 30
“The miR-33 family has two members in the human genome, miR-33b and miR-33a [78].”
BackgroundRegulation of HDL Genes: Transcriptional, Posttranscriptional, and Posttranslational
Kardassis, D., Gafencu, A. V., Zannis, V. I., & Dávalos, A. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-09665-0_3 · Cited by 30
“Although miR-33a and miR-33b target different genes involved in lipid homeostasis, fatty acid β-oxidation, insulin signaling, and biliary transporters (Gerin et al. 2010; Davalos et al. 2011; Rayner et al. 2011a; Allen et al. 2012; Horie et al. 2013), their effects are mediated mainly by ABCA1.”
BackgroundThe diverse roles of macrophages in metabolic inflammation and its resolution
Ray, A. G., Odum, O., Wiseman, D., & Weinstock, A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1147434 · Cited by 31
“, 2012), miR-33 (Gerin et al., 2010; Horie et al., 2010; Najafi-Shoushtari et al., 2010; Rayner et al., 2010; Rayner et al., 2011a; Rayner et al., 2011b), miR-106 (Kim et al.”
MicroRNAs and Lipoprotein Metabolism
Horie, T., Baba, O., Kuwabara, Y., Yokode, M., Kita, T., Kimura, T., & Ono, K. (2014) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.20859 · Cited by 29
The role of microRNAs in liver injury at the crossroad between hepatic cell death and regeneration
Lauschke, V. M., Mkrtchian, S., & Ingelman-Sundberg, M. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.10.084 · Cited by 29
Effects of hypoxic exercise training on microRNA expression and lipid metabolism in obese rat livers
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“Previous studies supported that overexpression of miRNA378/378* may up-regulate a series of lipogenic genes levels through increasing expression of PPARγ2, and then increase the size of the lipid droplets and the production of TG (Gerin et al., 2010b).”
BackgroundTXNIP regulates myocardial fatty acid oxidation via miR-33a signaling
Chen, J., Young, M. E., Chatham, J. C., Crossman, D. K., Dell’Italia, L. J., & Shalev, A. (2016) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00151.2016 · Cited by 28
Intersections of post-transcriptional gene regulatory mechanisms with intermediary metabolism
Arif, W., Datar, G. K., & Kalsotra, A. (2017) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2017.01.004 · Cited by 28
Metformin: On Ongoing Journey across Diabetes, Cancer Therapy and Prevention
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“human liver cells induces fatty acid degradation, through the lack of modulation in the expression of genes involved in the oxidation of fatty acid [56,57].”
BackgroundZhang, D., Wang, D., Wang, Z., Wang, Y., Li, G., Sun, G., Tian, Y., Han, R., Li, Z., Jiang, R., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051624 · Cited by 27
“The literature showed that gga-miR-33 can participate in lipid metabolism by targeting fat mass and obesity-associated (FTO) genes associated with obesity in chicken liver [1], and miR-33 can regulate cholesterol and fatty acid metabolism in mammals (humans and mice), which corresponds to the function of the host gene…”
BackgroundSmolka, C., Schlösser, D., Hohnloser, C., Bemtgen, X., Jänich, C., Schneider, L. A., Martin, J., Pfeifer, D., Moser, M., Hasselblatt, P., et al. (2021) · Molecular Medicine · doi:10.1186/s10020-021-00364-6 · Cited by 27
Sommerauer, C., & Kutter, C. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00232.2022 · Cited by 27
Tuersuntuoheti, M., Zhang, J., Zhou, W., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0283383 · Cited by 26
“MiR-33 was found to target the silencing of fatty acid β oxidation-related genes CROT and HADHB [20,21].”
BackgroundWang, W.-S., Du, Z.-Q., Cheng, B.-H., Wang, Y.-X., Yao, J., Li, Y.-M., Cao, Z.-P., Luan, P., Wang, N., & Li, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117843 · Cited by 30
Hepatic ELOVL6 mRNA is regulated by the gga-miR-22-3p in egg-laying hen
Ma, Z., Li, H., Zheng, H., Jiang, K., Yan, F., Tian, Y., Kang, X., Wang, Y., & Liu, X. (2017) · Gene · doi:10.1016/j.gene.2017.04.040 · Cited by 26
microRNA-33 controls hunger signaling in hypothalamic AgRP neurons
Price, N. L., Fernández-Tussy, P., Varela, L., Cardelo, M. P., Shanabrough, M., Aryal, B., de Cabo, R., Suárez, Y., Horvath, T. L., & Fernández-Hernando, C. (2024) · Nature Communications · doi:10.1038/s41467-024-46427-0 · Cited by 25
“…been shown to suppress numerous factors involved in mitochondrial biogenesis and function, including AMP-activated protein kinase subunit-a ( Prkaa1 ), peroxisome proliferator-activated receptor gamma, coactivator 1 alpha ( Ppargc1a ), and carnitine palmitoyl-transferase 1 ( Cpt1a ) 6,22 – 25 .”
Background
Metadata
- Authors
- Gerin, I., Clerbaux, L.-A., Haumont, O., Lanthier, N., Das, A. K., Burant, C. F., Leclercq, I. A., MacDougald, O. A., & Bommer, G. T.
- Affiliations
- de Duve Institute (BE)
- UCLouvain (BE)
- Michigan Medicine (US)
- University of Michigan (US)
- Corresponding author
- Bommer, Guido T.
- ORCID
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2010-10
- Volume
- 285
- Issue
- 44
- Pages
- 33652-33661
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC2962463
- OpenAlex
- W2012616814
- Cited by
- 382
- References
- 60
- Citations by year
- 2026: 12 · 2025: 10 · 2024: 14 · 2023: 16 · 2022: 17 · 2021: 29 · 2020: 15 · 2019: 18 · 2018: 24 · 2017: 25 · 2016: 42 · 2015: 28 · 2014: 36 · 2013: 50 · 2012: 23
- FWCI
- 29.85
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (submittedVersion)
- PubMed Central (submittedVersion)
- Digital Access to Libraries (submittedVersion)
- Funders
- Fonds pour la Formation à la Recherche dans l’Industrie et dans l’Agriculture
- National Institute of Diabetes and Digestive and Kidney Diseases (5P30DK089503, R01 DK051563, DK-51563, P30 DK089503)
- Michigan Nutrition Obesity Research Center, Medical School, University of Michigan
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- miR-33, SREBP2, intronic microRNA, ABCA1, cholesterol export, fatty acid beta-oxidation, CPT1A, HADHB, lipid homeostasis, SREBP, protein synthesis inhibition
- MeSH terms
- Animals, Cholesterol, Fatty Acids, Gene Expression Regulation, Humans, Introns, Male, Mice, Inbred C57BL, Phospholipids, Lentivirus, MicroRNAs, Mice, Sterol Regulatory Element Binding Protein 2
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