The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index; 7 of the 33 sources its claims cite were checked for support.
Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors
Open accessAbstract
Ten patients with refractory solid tumors received EZN-2968 18 mg/kg weekly for 3 weeks in a 6-week cycle; one patient had prolonged stable disease for 24 weeks, and 4 of 6 paired biopsies showed reduced HIF-1α mRNA.
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Claims the paper makes
25 Own result · 13 No full text of the sources · 5 Own method · 4 Own interpretation · 3 Supported · 2 Partly supported · 2 Couldn’t confirm · 2 No basis given · 1 Not checked yet · accuracy not yet measured
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“GLUT-1, known to be targeted by both HIF-1α and HIF-2α, was only decreased in 2 patients [19].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Could not verifycites [19] Keith B, Johnson RS, Simon MC (2012) HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression. Nat Rev Cancer 12:9–22 sourceExperimental — accuracy not yet measured
The passages from the review’s Acetylation and Differential stability sections discuss HIF activity and glucose transport, but do not report GLUT-1 decreasing in two patients. Searches for “GLUT-1,” “GLUT1,” and “two patients decreased expression” found no passage addressing that patient-level result. (LLM, conf=0.75)
plainn = 2- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Could not verify
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Because preclinical biodistribution studies of EZN-2968 documented prolonged and preferential retention in the liver [11]”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction > Patients and methods
What the sources say
- Partly supportedcites [11] Greenberger LM, Horak ID, Filpula D, Sapra P, Westergaard M, Frydenlund HF, Albaek C, Schroder H, Orum H (2008) A RNA antagonist of hypoxia-inducible factor-1 alpha, EZN-2968, inhibits tumor cell growth. Mol Cancer Ther 7:3598–3608 sourceExperimental — accuracy not yet measured
The Biodistribution and Tissue Half-life section reports prolonged retention in mice, with an estimated tissue half-life of about 200 hours, and identifies the liver as a major site of accumulation. It also reports broad distribution to several organs and similar half-lives across tissues, so it does not establish preferential retention in the liver. No page number is available in our copy. (LLM, conf=0.88)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Interestingly, the expression of VEGF, which is commonly considered a HIF-1α and HIF-2α target gene [19], was unchanged in all of the samples examined.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Supportedcites [19] Keith B, Johnson RS, Simon MC (2012) HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression. Nat Rev Cancer 12:9–22 source
Citation [19] is attached to the background description of VEGF as a HIF-1α and HIF-2α target, not to the citing authors’ observation that VEGF was unchanged in their samples. The source’s Therapy section links HIF-1α to VEGFA expression, and its “Assessing HIF1α and HIF2α function in tumor models” section reports increased VEGF expression with HIF-2α overexpression (page numbers unavailable). (LLM, conf=0.88)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Tumor growth inhibition was observed in xenograft models [11].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction
What the sources say
- Supportedcites [11] Greenberger LM, Horak ID, Filpula D, Sapra P, Westergaard M, Frydenlund HF, Albaek C, Schroder H, Orum H (2008) A RNA antagonist of hypoxia-inducible factor-1 alpha, EZN-2968, inhibits tumor cell growth. Mol Cancer Ther 7:3598–3608 source
The antitumor-effect results report significantly lower tumor weight in nude mice implanted with DU145 cells pretransfected with EZN-2968. The paper also notes that EZN-2968 given to mice without that pretransfection produced a small, statistically nonsignificant reduction; the claim is supported as an observation of tumor growth inhibition in a xenograft model, not as evidence that systemic treatment alone was effective. (LLM, conf=0.90)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“However, given the small number of patients on the trial and the fact that interrogation of the VEGF pathway was not part of the study, it is difficult to draw definitive conclusions about the antiangiogenic effects of EZN-2968 in humans [20].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Could not verifycites [20] Jeong W, Doroshow JH, Kummar S (2013) United States Food and Drug Administration approved oral kinase inhibitors for the treatment of malignancies. Curr Probl Cancer 37:110–144 sourceExperimental — accuracy not yet measured
Section 6 discusses VEGFR-inhibiting kinase inhibitors and their adverse reactions, but not EZN-2968. Searches for EZN-2968 and its antiangiogenic effects returned no passage about its trial, patient number, or whether the VEGF pathway was interrogated. Our copy therefore does not establish the attributed conclusion. (LLM, conf=0.77)
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Could not verify
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
“EZN-2968 was generally well tolerated without significant toxicity (Table 2).”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > Toxicity
- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: unclear — It is unclear why the paper says it holds.
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
“Five of the patients assessed had decreased HIF-1α mRNA copy numbers ranging from −7 to −94 % from baseline.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plainn = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“There were no new cases of hypertension in this study of EZN-2968”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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 second, a patient with Hurthle cell thyroid carcinoma (Patient #3), had 35 and 14 % increases in Ktrans and kep values, respectively.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > DCE-MRI
plaindirectSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“Reduction in HIF-1α mRNA levels compared to baseline was demonstrated in 4 of 6 patients with paired tumor biopsies.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Abstract > Results
boosteddirectn = 6- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 16
- Probably not a substantial claim. 8
Every source the paper cites for this claim was checked and supports it.
In the paper
“EZN-2968 is an LNA antisense oligodeoxynucleotide that has been demonstrated to hybridize with HIF-1α mRNA and block HIF-1α protein expression in preclinical models [11].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction
What the sources say
- Supportedcites [11] Greenberger LM, Horak ID, Filpula D, Sapra P, Westergaard M, Frydenlund HF, Albaek C, Schroder H, Orum H (2008) A RNA antagonist of hypoxia-inducible factor-1 alpha, EZN-2968, inhibits tumor cell growth. Mol Cancer Ther 7:3598–3608 source
The Results (Biophysical Properties) describe EZN-2968 as an LNA/DNA oligonucleotide complementary to HIF-1α mRNA and report its high affinity for that RNA. The Results (Effect on HIF-1α mRNA and Protein Expression in Tumor Cells) report that HIF-1α protein was nearly absent after treatment of cultured cells. Page numbers were not supplied. (LLM, conf=0.92)
direct- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“IC50 values for the HIF-2α isoform, with which EZN-2968 has a 3-base-pair mismatch, were 5 times higher in all cell lines tested compared to IC50 values for HIF-1α, supporting the relative selectivity of EZN-2968 for HIF-1α [11].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Partly supportedcites [11] Greenberger LM, Horak ID, Filpula D, Sapra P, Westergaard M, Frydenlund HF, Albaek C, Schroder H, Orum H (2008) A RNA antagonist of hypoxia-inducible factor-1 alpha, EZN-2968, inhibits tumor cell growth. Mol Cancer Ther 7:3598–3608 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly 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
“five patients had paired biopsies for the assessment of HIF-1α protein levels (Patients #1, 2, 3, 6, and 7; Fig. 1b)”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plainn = 5- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably 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
“Patient #2 had a discordant 113 % increase in HIF-1α protein and 30 % decrease in HIF-1α mRNA.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plainSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“Two patients had a decrease in levels of both HIF-1α mRNA and protein following EZN-2968 treatment, yet there was no corresponding decrease in the expression of the four HIF-1-targeted genes evaluated.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plainn = 2- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“EZN-2968 was well tolerated at the dose and schedule described; most of the toxicities were grade 1 or 2, and there were no unexpected toxicities.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“The first, a patient with rectal adenocarcinoma (Patient #1), had a 48 % decrease in Ktrans value and a 33 % decrease in kep value between baseline and post-treatment DCE-MRI.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > DCE-MRI
plainSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“We did not observe any cases of PTT prolongation, but one patient had a grade 2 infusion reaction attributed to complement activation.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plainSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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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
“There were no differences in clinical response between these two groups of patients or across various sites of metastases.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“Ten patients were enrolled”
- Also stated in: § Patient demographics · plain
“A total of 10 patients were enrolled (Table 1)”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Abstract > Results
plainn = 10- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Also stated in: § Patient demographics · 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
“In the limited number of patient samples available for analysis, there were no clear patterns of decreased expression as a result of EZN-2968 therapy, or overall associations with changes in either HIF-1α protein or mRNA levels.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > Expression of HIF-1α target genes
plain- Asserted: passes — The authors put it forward as true.
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- Based: passes — The paper gives a reason why it holds.
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
“Only one patient met the predefined study criteria of a greater than 50 % decrease in HIF-1α mRNA; however, sufficient tumor biopsy material was not available to perform protein analysis for this patient.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
plainSingle case- Asserted: passes — The authors put it forward as true.
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- Based: passes — The paper gives a reason why it holds.
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
“Patient #6 had increase in level of HIF-1α protein and mRNA”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plainSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
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
“Four patients (Patients #2, 3, 6, and 7) had both HIF-1α protein and mRNA copy number assessed.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plainn = 4- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably 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
“Three patients had decreased HIF-1α protein levels following EZN-2968 treatment, of which two (Patients #1 and #7) had a greater than 50 % decrease.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
plaindirectn = 3- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The enrollment goal was a total of 20 evaluable patients with paired biopsies and measurable HIF-1α protein levels.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction > Statistical analysis
plainn = 20- Asserted: passes — The authors put it forward as true.
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- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“HIF-1 is frequently overexpressed in cancer cells, where it is involved in the upregulation of many genes necessary for survival.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Abstract > Purpose
What the sources say
- Not checked — no full text of the sourcecites [1] Semenza GL (2003) Targeting HIF-1 for cancer therapy. Nat Rev Cancer 3:721–732 source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“For purposes of sample size determination, the primary endpoint was the proportion of patients in whom expression of HIF-1α mRNA in a tumor biopsy decreased by 50 % compared to baseline.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction > Statistical analysis
plain- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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Probably not a substantial claim.
In the paper
“Hepatic and renal toxicities have been reported previously with the administration of phosphorothioate antisense oligonucleotides, as have complement activation and prolongation of PTT due to interaction with complement and coagulation factor [16].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Not checked — no full text of the sourcecites [16] Levin AA (1999) A review of the issues in the pharmacokinetics and toxicology of phosphorothioate antisense oligonucleotides. Biochim Biophys Acta 1489:69–84 source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“This trial was conducted under a National Cancer Institute (NCI)-sponsored IND with Institutional Review Board approval. The protocol design and conduct followed all applicable regulations, guidance, and local policies (ClinicalTrials.gov Identifier: NCT01120288).”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction > Patients and methods
plain- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
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Probably not a substantial claim. The paper’s conclusions may not depend on it. It 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
“Reports in the literature demonstrate clusters of HIF-1α-positive cells at the edge of tumor margins, around necrotic regions and areas of neovascularization using immunohistochemical analysis [17, 18].”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Discussion
What the sources say
- Not checked — no full text of the sourcecites [17] Zhong H, De Marzo AM, Laughner E, Lim M, Hilton DA, Zagzag D, Buechler P, Isaacs WB, Semenza GL, Simons JW (1999) Overexpression of hypoxia-inducible factor 1α in common human cancers and their metastases. Cancer Res 59:5830–5835
- Not checked — no full text of the sourcecites [18] Talks KL, Turley H, Gatter KC, Maxwell PH, Pugh CW, Ratcliffe PJ, Harris AL (2000) The expression and distribution of the hypoxia-inducible factors HIF-1α and HIF-2α in normal human tissues, cancers, and tumor-associated macrophages. Am J Pathol 157:411–421 source
boosted- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Safety and a recommended Phase 2 dose was determined, and preliminary evidence of activity observed in two Phase 1 clinical trials of EZN-2968.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Introduction
What the sources say
- Not checked — no full text of the sourcecites [12] Patnaik A, Chiorean EG, Tolcher A, Papadopoulos K, Beeram M, Kee D, Waddell M, Gilles E, Buchbinder A (2009) EZN-2968, a novel hypoxia-inducible factor-1 (HIF-1) messenger ribonucleic acid (mRNA) antagonist: results of a phase I, pharmacokinetic (PK), dose-escalation study of daily administration in patients (pts) with advanced malignancies. J Clin Oncol 27:2564 source
- Not checked yetcites [13] Cohen RB, Olszanski A, Figueroa J, Hurwitz H, Lokiec FM, Rezaï K, Berkowitz N, Buchbinder A (2011) Down-modulation of messenger ribonucleic acid (mRNA) by EZN-2968, an hypoxia-inducible factor-1(HIF-1α) mRNA antagonist, administered in adult patients with advanced solid tumors [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research, Orlando, Florida. AACR, Philadelphia (PA), abstract nr LB-407, 2–6 April 2011
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper relies on this without support.
Changes in HIF-1α mRNA and protein levels in tumor biopsies are attributable to EZN-2968 rather than to other factors.
“This trial provides preliminary proof of concept for modulation of HIF-1α mRNA and protein expression and target genes in tumor biopsies following the administration of EZN-2968.”
The paper relies on this without support.
HIF-1 is a heterodimer of an oxygen-inducible HIF-1α subunit and a constitutively expressed HIF-1β subunit.
“HIF-1 is a heterodimer consisting of the HIF-1α subunit, inducible by tissue hypoxia, and the HIF-1β subunit, which is constitutively expressed.”
The paper relies on this without support.
Preclinical biodistribution findings in animals predict human liver delivery and target modulation.
“Because preclinical biodistribution studies of EZN-2968 documented prolonged and preferential retention in the liver [11], we initially restricted enrollment to patients with advanced solid tumors where the liver involvement represented the predominant disease burden to optimize our ability to demonstrate target modulation and provide clinical benefit (2 patients).”
The paper relies on this without support.
Anemia is a sensitive marker of erythropoietin suppression by EZN-2968.
“Only one case of grade 1 anemia was observed, which suggests that EZN-2968 did not suppress erythropoietin production in the kidney”
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 cited source doesn’t support the claim as written.
In the citing paper
“EZN-2968 has also been evaluated in two phase I clinical trials: results from one trial showed reduced HIF-1α mRNA in post-treatment biopsies from 4 out of 6 patients with paired tumor biopsies, and HIF-1α protein and mRNA levels of target genes were reduced in biopsies from two patients.”
From Therapeutic targeting of hypoxia and hypoxia-inducible factors in cancer (2016) · cites this paper as Jeong et al., 2014
Checked by a reasoning model — may be wrong.
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
“EZN-2968 binds specifically to HIF1A mRNA, promoting transcript degradation and inhibiting translation [280,281].”
From HIF inhibition: Current strategies and clinical challenges (2026) · cites this paper as [280]
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 these studies, EZN-2968 reduced HIF1A expression in 4 of 6 evaluable patients based on paired biopsies, with concomitant suppression of HIF-1 target genes in two cases and was generally well tolerated [39,280].”
From HIF inhibition: Current strategies and clinical challenges (2026) · cites this paper as [280]
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
“EZN-2968 is built on locked nucleic acid (LNA) chemistry, in which a methylene bridge between the 2′-oxygen and 4′-carbon of the ribose ring locks the sugar into a rigid conformation. This structural feature enhances base-pairing affinity, nuclease resistance, and in vivo stability relative to conventional oligonucleotides [[279], [280], [281]].”
From HIF inhibition: Current strategies and clinical challenges (2026) · cites this paper as [280]
Experimental — accuracy not yet measured
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.
Rated major: it would touch a result — a value a result rests on, reported and recomputed p-values on opposite sides of the significance level, two passages that conflict with no sign which is right, or a cited work retracted before this paper was published.
In the paper
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Abstract > Results
“Reduction in HIF-1α mRNA levels compared to baseline was demonstrated in 4 of 6 patients with paired tumor biopsies.”
§ Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1α), in patients with refractory solid tumors > Results > HIF-1α mRNA and protein levels
“Five of the patients assessed had decreased HIF-1α mRNA copy numbers ranging from −7 to −94 % from baseline.”
Citations
Cites
New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)
Eisenhauer, E. A., Therasse, P., Bogaerts, J., Schwartz, L. H., Sargent, D., Ford, R., Dancey, J., Arbuck, S., Gwyther, S., Mooney, M., et al. (2009) · European Journal of Cancer · doi:10.1016/j.ejca.2008.10.026 · Cited by 29,534 · cited 1×
“1 [14].”
Targeting HIF-1 for cancer therapy
Semenza, G. L. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1187 · Cited by 6,717 · cited 1×
“Hypoxia-inducible factor-1 (HIF-1), a transcription factor, facilitates tissue adaptation to oxygen deprivation by inducing the expression of genes necessary for cell survival [1].”
Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients
Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,836
(1999) · PubMed · Cited by 2,204
HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression
Keith, B., Johnson, R. S., & Simon, M. C. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3183 · Cited by 1,693 · cited 2×
“Interestingly, the expression of VEGF, which is commonly considered a HIF-1α and HIF2α target gene [19], was unchanged in all of the samples examined.”
BackgroundTalks, K. L., Turley, H., Gatter, K. C., Maxwell, P. H., Pugh, C. W., Ratcliffe, P. J., & Harris, A. L. (2000) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)64554-3 · Cited by 1,312 · cited 1×
“Reports in the literature demonstrate clusters of HIF-1α-positive cells at the edge of tumor margins, around necrotic regions and areas of neovascularization using immunohistochemical analysis [17, 18].”
BackgroundLNA (Locked Nucleic Acid): High-Affinity Targeting of Complementary RNA and DNA
Vester, B., & Wengel, J. (2004) · Biochemistry · doi:10.1021/bi0485732 · Cited by 727 · cited 1×
“Antisense oligonucleotides are an attractive therapeutic strategy because they can inhibit mRNA expression specifically [7, 8].”
BackgroundLevin, A. A. (1999) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(99)00140-2 · Cited by 438 · cited 2×
“One patient had a grade 2 infusion reaction that was attributed to complement activation, a known class effect of phosphorothioate-linked antisense oligodeoxynucleotides [16]; this toxicity resolved within a few hours after antihistamine and steroid treatment.”
Background(2002) · PubMed · Cited by 385
A RNA antagonist of hypoxia-inducible factor-1α, EZN-2968, inhibits tumor cell growth
Greenberger, L. M., Horak, I. D., Filpula, D., Sapra, P., Westergaard, M., Frydenlund, H. F., Albæk, C., Schrøder, H., & Ørum, H. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-08-0510 · Cited by 245 · cited 5×
“Tumor growth inhibition was observed in xenograft models [11].”
Influential
Cited by
Sorted by citations
Items 101–157 of 157
Hypoxia-induced alternative splicing in human diseases: the pledge, the turn, and the prestige
Natua, S., Ashok, C., & Shukla, S. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03727-0 · Cited by 22
Xun, Z., Zhou, H., Shen, M., Liu, Y., Sun, C., Du, Y., Jiang, Z., Yang, L., Zhang, Q. H., Lin, C., et al. (2024) · Advanced Science · doi:10.1002/advs.202309885 · Cited by 27
Research progress on non-protein-targeted drugs for cancer therapy
Zhang, Y., Lu, L., Song, F., Zou, X., Liu, Y., Zheng, X., Qian, J., Gu, C., Huang, P. C., & Yang, Y. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02635-y · Cited by 22
Akhenblit, P. J., & Pagel, M. D. (2016) · Journal of Cancer Science & Therapy · doi:10.4172/1948-5956.1000382 · Cited by 21
“The antisense oligodeoxynucleotide EZN-2968 demonstrated proof of concept viability as an inhibitor of HIF-1α in a phase I clinical trial with various refractory solid tumors, including colorectal, breast, pancreatic, adenoid cystic, mesothelioma, and Hurthle cell tumors, after showing promising results during in vivo…”
BackgroundLange, C., Lehnert, P., Boneva, S., Zhang, P., Ludwig, F., Boeker, M., Hoffmeier, K., Horres, R., Schlunck, G., Reinhard, T., et al. (2018) · Eye · doi:10.1038/s41433-018-0172-6 · Cited by 20
Jiang, W., Abdulkadir, S., Zhao, X., Sang, P., Τοματσίδου, Α., Zhang, X., Chen, Y., Calcul, L., Sun, X., Cheng, F., et al. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c06694 · Cited by 24
Kim, A., & Yeul, J. (2018) · Phytomedicine · doi:10.1016/j.phymed.2018.12.017 · Cited by 18
Zhang, Z., & Zhang, H. (2021) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2021.2015321 · Cited by 18
“Under hypoxic conditions, EZN-2968 treatment reduces the mRNA and protein levels of HIF-1α and significantly suppresses tumor growth in tumor-bearing mice [209], and phase I clinical trials demonstrated its efficacy and safety [210,211].”
BackgroundFarina, A. R., Cappabianca, L. A., Zelli, V., Sebastiano, M., & Mackay, A. R. (2021) · World Journal of Stem Cells · doi:10.4252/wjsc.v13.i7.685 · Cited by 19
Natural products as potent inhibitors of hypoxia-inducible factor-1α in cancer therapy
Zhong, J., Li, X., Lyu, W.-Y., Ye, W., & Zhang, D. (2020) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(20)60008-5 · Cited by 19
Bouhamida, E., Morciano, G., Pedriali, G., Ramaccini, D., Tremoli, E., Giorgi, C., Pinton, P., & Patergnani, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241311105 · Cited by 19
“factor kappa B (NF-κB) and Notch homolog 1, translocation-associated (Notch1) signaling pathways [73].”
BackgroundTherapeutic Strategies to Block the Hypoxic Response
DiGiacomo, J. W., & Gilkes, D. M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12734-3_10 · Cited by 16
Understanding the relationship between cancer associated cachexia and hypoxia-inducible factor-1
Muthamil, S., Kim, H. Y., Jang, H., Lyu, J., Shin, U. C., Go, Y., Park, S., Lee, H. G., & Park, J. H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114802 · Cited by 16
Self-citationMcDermott, A., & Tavassoli, A. (2024) · Transcription · doi:10.1080/21541264.2024.2417475 · Cited by 18
“…with patients with advanced tumors, EZN-2968 was able to decrease HIF-1α levels from biopsies though their sample size of patients was relatively small in both cases and in addition to the heterogeneity of the target, no statistically significant modulation of the target was validated [154,155].”
Synthetic RNA Therapeutics in Cancer
Han, Y., Shin, S.-H., Lim, C. G., Heo, Y. H., Choi, I. Y., & Kim, H. H. (2023) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.123.001587 · Cited by 14
Li, L., Ma, H., Li, D., Shu, Q., Wang, T., Song, X., & Xu, H. (2022) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2022.116246 · Cited by 13
Targeting HIF-1α in sickle cell disease and cancer: unraveling therapeutic opportunities and risks
Ubaid, S., Kashif, M., Laiq, Y., Nayak, A., Kumar, V., & Singh, V. K. (2024) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2024.2367640 · Cited by 13
Gene Regulation Using Nanodiscs Modified with HIF-1-α Antisense Oligonucleotides
Sharma, R., Dong, Y., Hu, Y., Ma, V. P.-Y., & Salaita, K. S. (2022) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.1c00505 · Cited by 9
Ma, M., Hu, R., Huang, Q., Zhong, X., Li, J., Lv, M., Yi, J., Sun, J., Fan, K., Xu, Y., et al. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107811 · Cited by 7
Song, L., Cai, J., Zhu, G., Zhang, P., Chen, S., Quan, B., Du, J.-X., Cai, Y., Song, L., Zhou, J., et al. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.218188 · Cited by 8
Synthesis and evaluation of biarylquinoline derivatives as novel HIF-1α inhibitors
Wu, Y., Lu, M., Lin, T.-H., Chu, P., & Chang, C. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.105681 · Cited by 7
Swearson, S., Rataan, A. O., Eliason, S. L., Amendt, B. A., Zakharia, Y., Salem, A. K., Ho, T. H., & Rustum, Y. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105604 · Cited by 7
Afşar, Ç. U., & Uysal, P. (2019) · Revista da Associação Médica Brasileira · doi:10.1590/1806-9282.65.10.1295 · Cited by 7
Myriad factors and pathways influencing tumor radiotherapy resistance
Mi, L., & Zhang, H. (2024) · Open Life Sciences · doi:10.1515/biol-2022-0992 · Cited by 8
“Despite extensive clinical trials conducted to date [98 – 101], no speci fi c HIF1 inhibitors have been adopted in general clinical practice [74,102].”
Roles of hypoxia in tumor progression and novel strategies for cancer treatment
Khan, B. D., Nhan, T. N. T., Chau, H. N. M., & Nhi, N. T. Y. (2022) · Biomedical Research and Therapy · doi:10.15419/bmrat.v9i10.774 · Cited by 8
Jensen, C. C., & Warfel, N. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820472-6.00039-6 · Cited by 5
Khoder, A. I., El-Sayed, I. H., & Ali, Y. B. M. (2025) · Medical Oncology · doi:10.1007/s12032-025-02935-7 · Cited by 4
“Advancement of LNA-anti-miR-32-5p as a therapeutic modality for malignant carcinoma of the breast, leverag-Medical ing the encouraging outcomes of previous LNA-based oligonucleotides in clinical studies [52, 53].”
Hypoxia-inducible factors link inflammation and lipid metabolism in atherosclerotic macrophages
Park, K. S., Ko, Y. J., & Choi, J.-H. (2026) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2026.1765661 · Cited by 5
Role of Hypoxia-Inducible Factor (HIF) in the Initiation of Cancer and Its Therapeutic Inhibitors
Eda, S. R., Vadde, R., & Jinka, R. (2017) · Springer eBooks · doi:10.1007/978-981-10-6728-0_10 · Cited by 3
RNAi-based Cancer Therapeutics: Are we there yet?
Saxena, V. (2014) · Journal of Pharmacovigilance · doi:10.4172/2329-6887.1000153 · Cited by 3
“Currently, there are many clinical trials in progress, most of them in Phase-I/IIa, evaluating the safety and efficacy of such siRNA-based drugs for cancer therapeutics [40-44].”
BackgroundHIF inhibition: Current strategies and clinical challenges
Więch-Walów, A., Bartoszewska, S., Barton, A., Czechowicz, P., Dudzik, J., Wielockx, B., Collawn, J. F., & Bartoszewski, R. (2026) · Redox biology · doi:10.1016/j.redox.2026.104220 · Cited by 3
“EZN-2968 binds specifically to HIF1A mRNA, promoting transcript degradation and inhibiting translation [280,281].”
Advances in antisense oligonucleotide treatment for cancer
Zhu, L., Muhtar, P., Goyama, S., & Yoshimi, A. (2026) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyag017 · Cited by 3
Targeted Delivery of Oligonucleotide–Peptide Conjugates for Enhanced Kidney-Specific Therapy
Mannes, M., Chigoho, D. M., Martin, C., Barlow, T. M. A., Hectors, T. L. M., Govaerts, T. C., Kayaert, P., Ridder, K. D., Delachaume, C., Vayssière, B., et al. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c01893 · Cited by 5
The pivotal role of metabolism in shaping tumor-associated macrophages phenotype and function
Jun, M., Li, T., Shi, Y., Yin, H., Wu, W., Dong, X. W., He, X., & Lai, X. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116547 · Cited by 1
Luo, T.-T., He, L.-X., Yin, Q., Wang, Z.-F., & Zuo, J. (2026) · Journal of Inflammation Research · doi:10.2147/jir.s600186 · Cited by 1
Larios-Martinez, K. I., Kosti, P., Schurich, A., Arnold, J. N., & Maher, J. F. (2020) · European Medical Journal · doi:10.33590/emj/20-00076 · Cited by 1
Targeted Gene Silencing in Malignant Hematolymphoid Cells Using GapmeR
Kizhakeyil, A., Fazil, M. H. U. T., & Verma, N. K. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0771-8_15 · Cited by 1
Targeting Hypoxic Adaptations of Cancer Cells: Molecular Mechanisms and Therapeutic Opportunities
Tang, C., & Yu, J. Q. (2014) · Springer eBooks · doi:10.1007/978-94-017-9421-3_14
Rad, E. (2015) · ORCA Online Research @Cardiff (Cardiff University)
The Tumor Microenvironment as a Target for Therapeutic Intervention
Hua, F., & DeClerck, Y. A. (2015) · Wiley eBooks · doi:10.1002/9781118468678.ch5
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Moehler, T. M., Hose, D., Andrulis, M., Seckinger, A., & Goldschmidt, H. (2019) · Springer eBooks · doi:10.1007/978-3-319-33673-2_34
The Clinical Impact of Hypoxia in Head and Neck Squamous Cell Carcinoma
Lim, A. M. L., Le, Q., & Rischin, D. (2018) · Current cancer research · doi:10.1007/978-3-319-78762-6_15
The Value of Anti-Angiogenics in Multiple Myeloma Therapy
Moehler, T. M., Hose, D., Andrulis, M., Seckinger, A., & Goldschmidt, H. (2017) · Springer eBooks · doi:10.1007/978-3-319-31215-6_34-1
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Li, W., & Zhang, J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-93064-2.00011-1
Jandick, N. A., Kirner, N. S., & Miller, C. L. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.10.540250
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Metadata
- Authors
- Jeong, W., Rapisarda, A., Park, S. R., Kinders, R. J., Chen, A., Melillo, G., Turkbey, B., Steinberg, S. M., Choyke, P., Doroshow, J. H., & Kummar, S.
- Affiliations
- National Cancer Institute (US)
- Frederick National Laboratory for Cancer Research (US)
- Corresponding author
- Kummar, Shivaani
- ORCID
- Venue
- Cancer Chemotherapy and Pharmacology
- Published
- 2013-11-30
- Volume
- 73
- Issue
- 2
- Pages
- 343-348
- ISSN
- 0344-5704 (ISSN-L)
- 1432-0843
- PMC
- PMC8375568
- OpenAlex
- W1986912321
- Cited by
- 159
- References
- 20
- Citations by year
- 2026: 8 · 2025: 10 · 2024: 9 · 2023: 18 · 2022: 14 · 2021: 19 · 2020: 22 · 2019: 8 · 2018: 13 · 2017: 12 · 2016: 12 · 2015: 9 · 2014: 5
- FWCI
- 3.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cancer Chemotherapy and Pharmacology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (HHSN261200800001C)
- National Cancer Institute (HHSN261200800001E), Z01BC010714, ZIABC011078)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Hepatology › Hepatocellular Carcinoma Treatment and Prognosis
- Keywords
- antisense oligonucleotides, hypoxia-inducible factor-1α, HIF-1α inhibition, refractory solid tumors, tumor hypoxia, HIF-1 target genes, tumor biopsy, dynamic contrast-enhanced MRI, duodenal neuroendocrine tumor
- MeSH terms
- Aged, Biopsy, Female, Humans, Infusions, Intravenous, Male, Middle Aged, Neoplasms, Oligonucleotides, Pilot Projects, RNA, Messenger, Oligonucleotides, Antisense, Cell Line, Tumor, Hypoxia-Inducible Factor 1
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