Evidence map›Paper›PMID 27882943›Full record

ArticleCell death & disease2016

Metadherin facilitates podocyte apoptosis in diabetic nephropathy.

Wen-Ting Liu, Fen-Fen Peng, Hong-Yu Li, Xiao-Wen Chen, Wang-Qiu Gong, Wen-Jing Chen, Yi-Hua Chen, Pei-Lin Li, Shu-Ting Li, Zhao-Zhong Xu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
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  4. miRNA in the Progression of Diabetic Kidney Disease: New Insight.International journal of molecular sciences · 2025
    Review
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  8. Article
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  16. MicroRNAs in kidney injury and disease.Nature reviews. Nephrology · 2022
    Review
  17. Article
  18. Article
  19. Activation of the NLRP3 inflammasome by RAC1 mediates a new mechanism in diabetic nephropathy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  20. Article
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

11 authors at 2 institutions in 1 country.

Wen-Ting LiuDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Fen-Fen PengDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Hong-Yu LiDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Xiao-Wen ChenDepartment of Nephrology, NanFang Hospital, Southern Medical University, Guangzhou 510515, China.
Wang-Qiu GongDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Wen-Jing ChenDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Yi-Hua ChenDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Pei-Lin LiDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Shu-Ting LiDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Zhao-Zhong XuDepartment of Emergency, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Hai-Bo LongDepartment of Nephrology, ZhuJiang Hospital, Southern Medical University, Guangzhou 510280, China.
Zhujiang Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis, one of the major causes of podocyte loss, has been reported to have a vital role in diabetic nephropathy (DN) pathogenesis, and understanding the mechanisms underlying the regulation of podocyte apoptosis is crucial. Metadherin (MTDH) is an important oncogene, which is overexpressed in most cancers and responsible for apoptosis, metastasis, and poor patient survival. Here we show that the expression levels of Mtdh and phosphorylated p38 mitogen-activated protein kinase (MAPK) are significantly increased, whereas those of the microRNA-30 family members (miR-30s) are considerably reduced in the glomeruli of DN rat model and in high glucose (HG)-induced conditionally immortalized mouse podocytes (MPC5). These levels are positively correlated with podocyte apoptosis rate. The inhibition of Mtdh expression, using small interfering RNA, but not Mtdh overexpression, was shown to inhibit HG-induced MPC5 apoptosis and p38 MAPK pathway, and Bax and cleaved caspase 3 expression. This was shown to be similar to the effects of p38 MAPK inhibitor (SB203580). Furthermore, luciferase assay results demonstrated that Mtdh represents the target of miR-30s. Transient transfection experiments, using miR-30 microRNA (miRNA) inhibitors, led to the increase in Mtdh expression and induced the apoptosis of MPC5, whereas the treatment with miR-30 miRNA mimics led to the reduction in Mtdh expression and apoptosis of HG-induced MPC5 cells in comparison with their respective controls. Our results demonstrate that Mtdh is a potent modulator of podocyte apoptosis, and that it represents the target of miR-30 miRNAs, facilitating podocyte apoptosis through the activation of HG-induced p38 MAPK-dependent pathway.

Indexed as

ApoptosisAnimalsBase SequenceCell LineDiabetic NephropathiesDisease Models, AnimalFemaleGene Knockdown TechniquesGlucoseMaleMAP Kinase Signaling SystemMembrane ProteinsMice, Inbred C57BLMicroRNAsModels, Biologicalp38 Mitogen-Activated Protein KinasesGlucoseMembrane ProteinsMicroRNAsMtdh protein, mousep38 Mitogen-Activated Protein KinasesRNA-Binding Proteins

Identifiers

PMID27882943
PMCPMC5260885
OpenAlexW2554941534

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Registered trials

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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.