Evidence map›Paper›PMID 31934284›Full record

ArticleAmerican journal of translational research2019

MicroRNA-205 inhibits the apoptosis of renal tubular epithelial cells via the PTEN/Akt pathway in renal ischemia-reperfusion injury.

Wu Chen, Yuan Ruan, Sheng Zhao, Jinzhuo Ning, Ting Rao, Weimin Yu, Xiangjun Zhou, Cong Liu, Yucheng Qi, Fan Cheng

Abstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 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

10 authors at 1 institution in 1 country.

Wu ChenDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Yuan RuanDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Sheng ZhaoDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Jinzhuo NingDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Ting RaoDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Weimin YuDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Xiangjun ZhouDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Cong LiuDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Yucheng QiDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Fan ChengDepartment of Urology, Renmin Hospital of Wuhan University Wuhan 430000, Hubei, P. R. China.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal ischemia-reperfusion injury (IRI) is the main cause of acute kidney injury (AKI). Many studies on renal IRI have been performed recently, but effective treatments are still lacking. Evidence exists that small endogenous noncoding RNAs are involved in the ischemia-reperfusion process. This article aims to investigate whether microRNA-205 (miR-205) is involved in this process and to determine its role in the hypoxia-induced injury of renal tubular epithelial cells (TECs). We found that miR-205 was significantly downregulated in rats with renal IRI and in HK-2 cells with hypoxia-reoxygenation injury (HRI) in vitro. In vitro, overexpression of intracellular miR-205 by transfection of a miR-205 mimic significantly reduced apoptosis, and this antiapoptotic effect was antagonized by a miR-205 inhibitor. Moreover, we confirmed that PTEN is a target of miR-205. miR-205 exerted its protective effect by inhibiting HK-2 cell apoptosis and promoting HK-2 cell proliferation by inhibiting the expression of PTEN during HRI, and this protective effect was blocked by silencing PTEN. Therefore, we confirmed that miR-205 may target the PTEN/Akt signaling pathway to alleviate hypoxia-induced renal cell damage. miR-205 may be a new potential target for the treatment of renal IRI.

Indexed as

apoptosisMiR-205PTEN/Aktrenal ischemia-reperfusion injury

Identifiers

PMID31934284
PMCPMC6943442
OpenAlexW3006476723

What OpenQuestion holds

Textmetadata
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.