Evidence map›Paper›PMID 29636888›Full record

ArticleAmerican journal of translational research2018

MicroRNA-134-5p promotes high glucose-induced podocyte apoptosis by targeting bcl-2.

Xiaoxiao Qian, Juan Tan, Ling Liu, Sheng Chen, Na You, Huijuan Yong, Minglin Pan, Qiang You, Dafa Ding, Yibing Lu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Long non-coding RNA FAM99A modulated YAP1 to affect trophoblast cell behaviors in preeclampsia by sponging miR-134-5p.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
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  16. [NFAT2 mediates high glucose-induced apoptosis in glomerular podocytesNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
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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 2 institutions in 1 country.

Xiaoxiao QianDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Juan TanDepartment of Gerontology, Huai'an First People's Hospital, Nanjing Medical UniversityHuai'an 223300, China.
Ling LiuDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Sheng ChenDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Na YouDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Huijuan YongDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Minglin PanDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Qiang YouDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Dafa DingDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Yibing LuDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, China.
Second Affiliated Hospital of Nanjing Medical University · CNHuaian First People’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Podocyte apoptosis is a typical early feature of diabetic nephropathy (DN), with loss of nephrin integrity contributing to increased proteinuria in patients with DN. Emerging evidence shows that microRNAs (miRNAs) play vital roles in the pathogenesis of DN. Thus, we aimed to further elucidate the role of miRNAs in podocyte apoptosis in DN. We used db/db and db/m mice maintained under a continuous feeding regime for 12 weeks. Using microarray analysis, we found several miRNAs potentially related to podocyte apoptosis. In addition, we cultured a conditionally immortalized human podocyte cell line in 30 mM D-glucose and found that miR-134-5p was upregulated in both db/db mice and high-glucose (HG)-treated podocytes. Upregulation of miR-134-5p was accompanied by podocyte apoptosis and downregulation of nephrin. Inhibition of miR-134-5p produced the opposite effect. Dual-luciferase reporter assays showed that miR-134-5p directly targeted the 3'-untranslated region of the B-cell lymphoma-2 gene (BCL2), and further study confirmed an increase in bcl-2 protein level in HG-treated podocytes transfected with anti-miR-134-5p. Knockdown of BCL2 impeded the antiapoptotic effect of anti-miR-134-5p. Finally, we found that miR-134-5p might regulate apoptosis in db/db mice and podocytes by targeting BCL2. Taken together, our findings suggest that miR-134-5p promotes podocyte apoptosis under HG conditions by targeting BCL2. Our study provides a meaningful approach to interpret the mechanisms of action of miRNAs involved in DN.

Indexed as

apoptosisBCL2Diabetic nephropathyhigh glucosemicroRNApodocyte

Identifiers

PMID29636888
PMCPMC5883139
OpenAlexW2979913981

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.