Evidence map›Paper›PMID 31480879›Full record

ArticleJournal of the American Heart Association2019

Effect of HIF-1α/miR-10b-5p/PTEN on Hypoxia-Induced Cardiomyocyte Apoptosis.

Liping Wu, Yafen Chen, Yuanyuan Chen, Wenbo Yang, Yanxin Han, Lin Lu, Ke Yang, Jiumei Cao

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Liping WuDepartment of Geratology Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China.
Yafen ChenDepartment of Geratology Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China.
Yuanyuan ChenInstitute of Cardiovascular Disease Shanghai Jiao Tong University School of Medicine Shanghai China.
Wenbo YangInstitute of Cardiovascular Disease Shanghai Jiao Tong University School of Medicine Shanghai China.
Yanxin HanInstitute of Cardiovascular Disease Shanghai Jiao Tong University School of Medicine Shanghai China.
Lin LuInstitute of Cardiovascular Disease Shanghai Jiao Tong University School of Medicine Shanghai China.
Ke YangInstitute of Cardiovascular Disease Shanghai Jiao Tong University School of Medicine Shanghai China.
Jiumei CaoDepartment of Geratology Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China.
Ruijin Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Few reports have addressed the mechanism by which microRNA miR-10b-5p regulates post-myocardial infarction (post-MI) cardiomyocyte apoptosis under hypoxic conditions. Methods and Results C57BL/6 mice underwent surgical ligation of the left anterior descending artery to create an MI or ischemia/reperfusion animal model. The expression of miR-10b-5p, PTEN (phosphatase and tensin homolog), and HIF-1α (hypoxia-inducible factor 1α) was detected in infarct border zone tissues at various time points. After precordial injections of the negative control or miR-10b-5p, overexpression lentiviruses were made in the areas surrounding the MI sites at 1 week, and myocardial infarct size, cardiac function, and cardiomyocyte apoptosis were examined. A miR-10b-5p mimic was transfected into primary mouse cardiomyocytes to analyze its effects on cardiomyocyte apoptosis and PTEN expression. Meanwhile, PTEN as a target of miR-10b-5p was verified via luciferase reporter gene assays. Cotransfection of miR-10b-5 and PTEN verified the relationship between miR-10b-5 and PTEN. Under hypoxic stress, the expression of HIF-1α and miR-10b-5p was examined. The results showed that miR-10b-5p expression was markedly reduced in the infarct border zone. Overexpression of miR-10b-5p in the murine model of MI significantly reduced MI size, improved cardiac function, and inhibited apoptosis. Overexpression of miR-10b-5p in vitro antagonized hypoxia-induced cardiomyocyte apoptosis and specifically inhibited the expression of the apoptosis-related gene PTEN, but overexpression of PTEN weakened these effects. We also found that hypoxia-induced accumulation of HIF-1α resulted in decreased expression of miR-10b-5p. Interfering with the activation of the HIF-1α signaling pathway promoted Pri-miR-10b and miR-10b-5p expression and inhibited PTEN expression. Conclusions MicroRNA miR-10b-5p antagonizes hypoxia-induced cardiomyocyte apoptosis, indicating that miR-10b-5p may serve as a potential future clinical target for the treatment of MI.

Indexed as

AnimalsApoptosisHypoxiaHypoxia-Inducible Factor 1, alpha SubunitMiceMice, Inbred C57BLMicroRNAsMyocardial InfarctionMyocardial Reperfusion InjuryMyocytes, CardiacPTEN PhosphohydrolaseHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN10 microRNA, mousePTEN PhosphohydrolasePten protein, mouseacute myocardial infarctionapoptosishypoxia‐inducible factor 1αmicroRNA miR‐10b‐5pphosphatase and tensin homolog

Identifiers

PMID31480879
PMCPMC6818010
OpenAlexW2971367862

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.