Evidence map›Paper›PMID 33939247›Full record

ArticleJournal of cellular and molecular medicine2021

LncRNA lnc-ISG20 promotes renal fibrosis in diabetic nephropathy by inducing AKT phosphorylation through miR-486-5p/NFAT5.

Yu-Rui Duan, Bao-Ping Chen, Fang Chen, Su-Xia Yang, Chao-Yang Zhu, Ya-Li Ma, Yang Li, Jun Shi

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Article
  3. Post‑translational modifications in diabetic kidney disease (Review).International journal of molecular medicine · 2026
    Review
  4. Article
  5. Article
  6. Article
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  8. Unlocking the therapeutic potential of the NFAT pathway in kidney diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
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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 1 institution in 1 country.

Yu-Rui DuanDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Bao-Ping ChenDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Fang ChenDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Su-Xia YangDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Chao-Yang ZhuDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Ya-Li MaDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.
Yang LiDepartment of Urology, Huaihe Hospital of Henan University, Kaifeng, China.
Jun ShiDepartment of Nephrology, Huaihe Hospital of Henan University, Kaifeng, China.ORCID 0000-0001-9429-5169
Henan University Huaihe Hospital and Huaihe Clinical Institute · CN

Funding

the Project of Henan Provincial Education Department 16A320031
6 · The paper itself

Abstract

Long non-coding RNA (lncRNA) lnc-ISG20 has been found aberrantly up-regulated in the glomerular in the patients with diabetic nephropathy (DN). We aimed to elucidate the function and regulatory mechanism of lncRNA lnc-ISG20 on DN-induced renal fibrosis. Expression patterns of lnc-ISG20 in kidney tissues of DN patients were determined by RT-qPCR. Mouse models of DN were constructed, while MCs were cultured under normal glucose (NG)/high glucose (HG) conditions. The expression patterns of fibrosis marker proteins collagen IV, fibronectin and TGF-β1 were measured with Western blot assay. In addition, the relationship among lnc-ISG20, miR-486-5p, NFAT5 and AKT were analysed using dual-luciferase reporter assay and RNA immunoprecipitation. The effect of lnc-ISG20 and miR-486/NFAT5/p-AKT axis on DN-associated renal fibrosis was also verified by means of rescue experiments. The expression levels of lnc-ISG20 were increased in DN patients, DN mouse kidney tissues and HG-treated MCs. Lnc-ISG20 silencing alleviated HG-induced fibrosis in MCs and delayed renal fibrosis in DN mice. Mechanistically, miR-486-5p was found to be a downstream miRNA of lnc-ISG20, while miR-486-5p inhibited the expression of NFAT5 by binding to its 3'UTR. NFAT5 overexpression aggravated HG-induced fibrosis by stimulating AKT phosphorylation. However, NFAT5 silencing reversed the promotion of in vitro and in vivo fibrosis caused by lnc-ISG20 overexpression. Our collective findings indicate that lnc-ISG20 promotes the renal fibrosis process in DN by activating AKT through the miR-486-5p/NFAT5 axis. High-expression levels of lnc-ISG20 may be a useful indicator for DN.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diabetic NephropathiesExoribonucleasesFemaleFibrosisHumansKidney DiseasesMaleMiceMice, Inbred C57BLMicroRNAsMiddle AgedPhosphorylationPrognosisExoribonucleasesISG20 protein, humanMicroRNAsMIRN486 microRNA, humanNFAT5 protein, humanProto-Oncogene Proteins c-aktRNA, Long NoncodingTranscription FactorsAKTdiabetic nephropathyfibrosisLnc-ISG20MicroRNA-486-5pNFAT5

Identifiers

PMID33939247
PMCPMC8178263
OpenAlexW3157410481

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.