Evidence map›Paper›PMID 30394845›Full record

ArticleCell cycle (Georgetown, Tex.)2018

MiR-130a-5p prevents angiotensin II-induced podocyte apoptosis by modulating M-type phospholipase A2 receptor.

Dongwei Liu, Fengxun Liu, Xutong Wang, Yingjin Qiao, Shaokang Pan, Yang Yang, Yifang Hu, Yilin Zhang, Fei Tian, Zhangsuo Liu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. MicroRNAs in kidney injury and disease.Nature reviews. Nephrology · 2022
    Review
  13. Review
  14. Novel Biomarkers in Membranous Nephropathy.Frontiers in immunology · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. MicroRNAs as Biomarkers for Nephrotic Syndrome.International journal of molecular sciences · 2020
    Review
  19. Review
  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

10 authors at 3 institutions in 1 country.

Dongwei Liua Department of Nephrology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou China.
Fengxun Liub Research Institute of Nephrology , Zhengzhou University , Zhengzhou China.
Xutong Wangb Research Institute of Nephrology , Zhengzhou University , Zhengzhou China.
Yingjin Qiaoa Department of Nephrology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou China.
Shaokang Pana Department of Nephrology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou China.
Yang Yanga Department of Nephrology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou China.
Yifang Hub Research Institute of Nephrology , Zhengzhou University , Zhengzhou China.
Yilin Zhangb Research Institute of Nephrology , Zhengzhou University , Zhengzhou China.
Fei Tianb Research Institute of Nephrology , Zhengzhou University , Zhengzhou China.
Zhangsuo Liua Department of Nephrology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou China.
Zhengzhou University · CNNational Clinical Research Center for Digestive Diseases · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Podocyte apoptosis is considered as the important element that promotes the development and progress of membranous nephropathy (MN). Unfortunately, the underlying mechanism of podocytes apoptosis in MN remains elusive. We compared the renal expressions of miR-130a-5p and M-type phospholipase A2 receptor (PLA2R) between MN patients (n = 30) and 30 controls by qRT-PCR and western blot, respectively. The podocyte damage model in vitro was established by angiotensin II (Ang II, 100 nmol/L) exposure for 24 h. Interaction between miR-130a-5p and PLA2R was determined using dual-luciferase reporter gene assay. MN mice were induced by intravenous injection of cBSA. In this study, miR-130a-5p expression was significantly decreased both in the renal biopsy specimens from MN patients and podocyte cell line AB8/13 following stimulation of Ang II. Overexpressed miR-130a-5p in AB8/13 cells significantly attenuated the Ang II induced-apoptosis in vitro. In contrast, down-regulated miR-130a-5p induced podocyte apoptosis. PLA2R was identified as the target of miR-130a-5p in AB8/13 cells. And up-regulated or down-regulated PLA2R could obviously attenuate the effect of miR-130a-5p overexpression or knockdown on the apoptosis of AB8/13 cells. Furthermore, it was also observed that overexpressed miR-130a-5p by miR-130a-5p agomir could obviously alleviate renal injury in MN mice. In conclusion, decreased miR-130a-5p was contributed to the pathological mechanism of MN through increasing PLA2R expression, which induced podocyte apoptosis.

Indexed as

Angiotensin IIAnimalsAntagomirsApoptosisCase-Control StudiesCell LineDisease Models, AnimalFemaleGlomerulonephritis, MembranousHumansMice, Inbred BALB CMicroRNAsPodocytesReceptors, Phospholipase A2Signal TransductionAngiotensin IIAntagomirsMicroRNAsMIRN130 microRNA, humanMIRN130 microRNA, mousePLA2R1 protein, humanPla2r1 protein, mouseReceptors, Phospholipase A2Membranous nephropathyMiR-130a-5pPLA2R

Identifiers

PMID30394845
PMCPMC6342077
OpenAlexW2899910282

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.