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miR-27b inhibits LDLR and ABCA1 expression but does not influence plasma and hepatic lipid levels in mice

Goedeke, Leigh, Rotllan, Noemi, Ramírez, Cristina M., Aranda, Juan F., Canfrán-Duque, Alberto, Araldi, Elisa, Fernández-Hernando, Ana, Langhi, Cedric, de Cabo, Rafael, Baldán, Ángel, Suárez, Yajaira, Fernández-Hernando, Carlos·2015·Atherosclerosis

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Crossref · 10.1016/j.atherosclerosis.2015.09.033

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  • Numerous miRNAs directly bind LDLR mRNA 3′UTR and decrease its expression, including miR-27a, miR-27b, miR-128-1, miR-128-3p, miR-130b, miR-148a, miR-184a, miR-185, and miR-301b.

    “Numerous miRNAs have been shown to directly bind LDLR mRNA 3' UTR and decrease its expression (Fig. 2), including miR-27a, miR-27b, miR-128-1, miR-128-3p, miR-130b, miR-148a, miR-184a, miR-185, and miR-301b [43][44][45][46][47][48].”

    From The low-density lipoprotein receptor: Emerging post-transcriptional regulatory mechanisms (2025) · cites this paper as [45]

    The Results (page unavailable) show that miR-27b reduces human LDLR 3′UTR reporter activity and LDLR expression. The Discussion (page unavailable) also reports that miR-27a directly regulates LDLR, but the copy does not establish the claim for the other seven listed miRNAs. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • The 3'UTR of LDLR contains one predicted miR-27b binding site at position 2472-2478 (ACUGUGA).

    “The 3’UTR of LDLR contains one predicted miR-27b binding site at position 2472-2478 (ACUGUGA)57.”

    From Pathways and Molecular Mechanisms Governing LDL Receptor Regulation (2025) · cites this paper as [57]

    The Results section states that the human LDLR 3′UTR has one conserved predicted miR-27b binding site. Our copy does not give the claimed position (2472–2478) or sequence (ACUGUGA), so those details remain unsupported. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • miR-27a, miR-27b, miR-128-1, miR-128-3p, miR-130b, miR-148a, miR-184a, miR-185, and miR-301b inhibit expression of the LDLR, decreasing LDLR.

    “miR-27a, miR-27b, miR-128-1, miR-128-3p, miR-130b, miR-148a, miR-184a, miR-185, miR-301b Inhibit expression of the LDLR ↓ [43-48]”
  • C57BL/6 mice treated with an AAV expressing the precursor of miR-27b had lower hepatic LDLR protein expression.

    “Additionally, C57BL/6 mice treated with an AAV expressing the precursor of miR-27b had lower hepatic LDLR protein expression57.”
  • Goedeke et al. demonstrated that miR-27b regulates LDLR expression using luciferase reporter assays in Cos7 cells, where addition of miR-27b decreased luciferase activity, but mutation of the predicted binding sites reversed this effect.

    “Goedeke et. al. demonstrated that miR-27b regulates LDLR expression using luciferase reporter assays in Cos7 cells, where addition of miR-27b decreased luciferase activity, but mutation of the predicted binding sites reversed this effect57.”

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Research works printed but not linked: 39

  1. Lusis, 2000, Atheroscler. Nat., 407, 233
  2. Glass, 2001, Atherosclerosis. the road ahead, Cell, 104, 503, 10.1016/S0092-8674(01)00238-0 · DOI
  3. Gould, 1998, Cholesterol reduction yields clinical benefit: impact of statin trials, Circulation, 97, 946, 10.1161/01.CIR.97.10.946 · DOI · Paper page
  4. Sjouke, 2011, Familial hypercholesterolemia: present and future management, Curr. Cardiol. Rep., 13, 527, 10.1007/s11886-011-0219-9 · DOI
  5. Hennekens, 1998, Increasing burden of cardiovascular disease: current knowledge and future directions for research on risk factors, Circulation, 97, 1095, 10.1161/01.CIR.97.11.1095 · DOI
  6. Brown, 1976, Receptor-mediated control of cholesterol metabolism, Science, 191, 150, 10.1126/science.174194 · DOI · Paper page
  7. Brown, 1986, A receptor-mediated pathway for cholesterol homeostasis, Science, 232, 34, 10.1126/science.3513311 · DOI · Paper page
  8. Brown, 1974, Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity, Proc. Natl. Acad. Sci. U. S. A., 71, 788, 10.1073/pnas.71.3.788 · DOI
  9. Maxfield, 2005, Role of cholesterol and lipid organization in disease, Nature, 438, 612, 10.1038/nature04399 · DOI
  10. Brown, 1997, The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor, Cell, 89, 331, 10.1016/S0092-8674(00)80213-5 · DOI · Paper page
  11. Goldstein, 1990, Regulation of the mevalonate pathway, Nature, 343, 425, 10.1038/343425a0 · DOI · Paper page
  12. Beaven, 2006, Nuclear receptors in lipid metabolism: targeting the heart of dyslipidemia, Annu. Rev. Med., 57, 313, 10.1146/annurev.med.57.121304.131428 · DOI
  13. Ambros, 2004, The functions of animal microRNAs, Nature, 431, 350, 10.1038/nature02871 · DOI · Paper page
  14. Bartel, 2009, MicroRNAs: target recognition and regulatory functions, Cell, 136, 215, 10.1016/j.cell.2009.01.002 · DOI · Paper page
  15. Filipowicz, 2008, Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?, Nat. Rev. Genet., 9, 102, 10.1038/nrg2290 · DOI
  16. Rayner, 2010, MiR-33 contributes to the regulation of cholesterol homeostasis, Science, 328, 1570, 10.1126/science.1189862 · DOI · Paper page
  17. Vickers, 2013, MicroRNA-27b is a regulatory hub in lipid metabolism and is altered in dyslipidemia, Hepatology, 57, 533, 10.1002/hep.25846 · DOI
  18. Chen, 2012, The magic and mystery of microRNA-27 in atherosclerosis, Atherosclerosis, 222, 314, 10.1016/j.atherosclerosis.2012.01.020 · DOI
  19. Zhang, 2014, MicroRNA-27a/b regulates cellular cholesterol efflux, influx and esterification/hydrolysis in THP-1 macrophages, Atherosclerosis, 234, 54, 10.1016/j.atherosclerosis.2014.02.008 · DOI
  20. Li, 2011, Identification of miR-130a, miR-27b and miR-210 as serum biomarkers for atherosclerosis obliterans, Clin. Chim. Acta, 412, 66, 10.1016/j.cca.2010.09.029 · DOI
  21. Staszel, 2011, Role of microRNAs in endothelial cell pathophysiology, Pol. Arch. Med. Wewn., 121, 361, 10.20452/pamw.1093 · DOI
  22. Oram, 2000, ABCA1-mediated transport of cellular cholesterol and phospholipids to HDL apolipoproteins, Curr. Opin. Lipidol., 11, 253, 10.1097/00041433-200006000-00005 · DOI
  23. Wang, 2010, Systematic evaluation of AAV vectors for liver directed gene transfer in murine models, Mol. Ther., 18, 118, 10.1038/mt.2009.246 · DOI
  24. Kassim, 2013, Adeno-associated virus serotype 8 gene therapy leads to significant lowering of plasma cholesterol levels in humanized mouse models of homozygous and heterozygous familial hypercholesterolemia, Hum. Gene Ther., 24, 19, 10.1089/hum.2012.108 · DOI
  25. Dietschy, 1993, Role of liver in the maintenance of cholesterol and low density lipoprotein homeostasis in different animal species, including humans, J. Lipid Res., 34, 1637, 10.1016/S0022-2275(20)35728-X · DOI · Paper page
  26. Kim, 2010, miR-27a is a negative regulator of adipocyte differentiation via suppressing PPARgamma expression, Biochem. Biophys. Res. Commun., 392, 323, 10.1016/j.bbrc.2010.01.012 · DOI
  27. Karbiener, 2009, microRNA miR-27b impairs human adipocyte differentiation and targets PPARgamma, Biochem. Biophys. Res. Commun., 390, 247, 10.1016/j.bbrc.2009.09.098 · DOI · Paper page
  28. Kida, 2011, PPARalpha is regulated by miR-21 and miR-27b in human liver, Pharm. Res., 28, 2467, 10.1007/s11095-011-0473-y · DOI
  29. Shirasaki, 2013, MicroRNA-27a regulates lipid metabolism and inhibits hepatitis C virus replication in human hepatoma cells, J. Virol., 87, 5270, 10.1128/JVI.03022-12 · DOI
  30. Gonzalez-Baro, 2007, Regulation of triglyceride metabolism. II. Function of mitochondrial GPAT1 in the regulation of triacylglycerol biosynthesis and insulin action, Am. J. Physiol. Gastrointest. Liver Physiol., 292, 10.1152/ajpgi.00553.2006 · DOI
  31. Rotllan, 2013, Therapeutic silencing of microRNA-33 inhibits the progression of atherosclerosis in Ldlr-/- mice–brief report, Arterioscler. Thromb. Vasc. Biol., 33, 1973, 10.1161/ATVBAHA.113.301732 · DOI · Paper page
  32. Suarez, 2007, Dicer dependent microRNAs regulate gene expression and functions in human endothelial cells, Circ. Res., 100, 1164, 10.1161/01.RES.0000265065.26744.17 · DOI
  33. Calvo, 1998, Human CD36 is a high affinity receptor for the native lipoproteins HDL, LDL, and VLDL, J. Lipid Res., 39, 777, 10.1016/S0022-2275(20)32566-9 · DOI
  34. Suarez, 2004, Synergistic upregulation of low-density lipoprotein receptor activity by tamoxifen and lovastatin, Cardiovasc. Res., 64, 346, 10.1016/j.cardiores.2004.06.024 · DOI
  35. Ramirez, 2011, MicroRNA-758 regulates cholesterol efflux through posttranscriptional repression of ATP-binding cassette transporter A1, Arterioscler. Thromb. Vasc. Biol., 31, 2707, 10.1161/ATVBAHA.111.232066 · DOI · Paper page
  36. Allen, 2014, Control of very low-density lipoprotein secretion by N-ethylmaleimide-sensitive factor and miR-33, Circ. Res., 115, 10.1161/CIRCRESAHA.115.303100 · DOI · Paper page
  37. Mattison, 2014, Resveratrol prevents high fat/sucrose diet-induced central arterial wall inflammation and stiffening in nonhuman primates, Cell Metab., 20, 183, 10.1016/j.cmet.2014.04.018 · DOI
  38. Shimomura, 1999, Increased levels of nuclear SREBP-1c associated with fatty livers in two mouse models of diabetes mellitus, J. Biol. Chem., 274, 30028, 10.1074/jbc.274.42.30028 · DOI
  39. Horton, 1998, Regulation of sterol regulatory element binding proteins in livers of fasted and refed mice, Proc. Natl. Acad. Sci. U. S. A., 95, 5987, 10.1073/pnas.95.11.5987 · DOI · Paper page

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Metadata

Authors
Goedeke, L., Rotllan, N., Ramírez, C. M., Aranda, J. F., Canfrán-Duque, A., Araldi, E., Fernández-Hernando, A., Langhi, C., de Cabo, R., Baldán, Á., Suárez, Y., & Fernández-Hernando, C.
Venue
Atherosclerosis
Publisher
Elsevier BV
Published
2015-12
Volume
243
Issue
2
Pages
499-509
ISSN
0021-9150
Cited by
65
References
2
Language
en
Funders
  • National Institutes of Health (R01HL107953, R01HL107953-04S1, R01HL106063, R01HL105945, 1F31AG043318, R01HL107794)
  • American Heart Association (15SDG23000025, GRNT20460189)

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