Evidence map›Paper›PMID 30187999›Full record

ArticleJournal of cellular and molecular medicine2018

Plectin protects podocytes from adriamycin-induced apoptosis and F-actin cytoskeletal disruption through the integrin α6β4/FAK/p38 MAPK pathway.

Yongliang Ni, Xin Wang, Xiaoxuan Yin, Yan Li, Xigao Liu, Haixin Wang, Xiangjv Liu, Jun Zhang, Haiqing Gao, Benkang Shi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  6. Cytoskeleton Rearrangement in Podocytopathies: An Update.International journal of molecular sciences · 2024
    Review
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  8. Article
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  14. Podocytes are lost from glomeruli before completing apoptosis.American journal of physiology. Renal physiology · 2022
    Article
  15. Article
  16. Article
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  19. 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

11 authors at 5 institutions in 1 country.

Yongliang NiDepartment of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Xin WangDepartment of Urology, Tengzhou Central People's Hospital affiliated to Jining Medical College, Xintan Road 181, Tengzhou, China.
Xiaoxuan YinDepartment of Traditional Chinese Medicine, Yankuang Group General Hospital, Zoucheng, China.
Yan LiDepartment of Urology, Qilu Hospital of Shandong University, Jinan, China.
Xigao LiuDepartment of Urology, Qilu Hospital of Shandong University, Jinan, China.
Haixin WangDepartment of Urology, Yankuang Group General Hospital, Zoucheng, China.
Xiangjv LiuDepartment of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Jun ZhangDepartment of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Haiqing GaoDepartment of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Benkang ShiDepartment of Urology, Qilu Hospital of Shandong University, Jinan, China.
Shaohua ZhaoDepartment of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Qilu Hospital of Shandong University · CNJining Medical University · CNShandong Provincial Hospital · CNYankuang Energy Group Company Limited (China)Zoucheng People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Podocyte injury is an early pathological change characteristic of various glomerular diseases, and apoptosis and F-actin cytoskeletal disruption are typical features of podocyte injury. In this study, we found that adriamycin (ADR) treatment resulted in typical podocyte injury and repressed plectin expression. Restoring plectin expression protected against ADR-induced podocyte injury whereas siRNA-mediated plectin silencing produced similar effects as ADR-induced podocyte injury, suggesting that plectin plays a key role in preventing podocyte injury. Further analysis showed that plectin repression induced significant integrin α6β4, focal adhesion kinase (FAK) and p38 MAPK phosphorylation. Mutating Y1494, a key tyrosine residue in the integrin β4 subunit, blocked FAK and p38 phosphorylation, thereby alleviating podocyte injury. Inhibitor studies demonstrated that FAK Y397 phosphorylation promoted p38 activation, resulting in podocyte apoptosis and F-actin cytoskeletal disruption. In vivo studies showed that administration of ADR to rats resulted in significantly increased 24-hour urine protein levels along with decreased plectin expression and activated integrin α6β4, FAK, and p38. Taken together, these findings indicated that plectin protects podocytes from ADR-induced apoptosis and F-actin cytoskeletal disruption by inhibiting integrin α6β4/FAK/p38 pathway activation and that plectin may be a therapeutic target for podocyte injury-related glomerular diseases.

Indexed as

Actin CytoskeletonActinsAnimalsApoptosisDoxorubicinFocal Adhesion Kinase 1HumansIntegrin alpha6beta4KidneyKidney GlomerulusMicep38 Mitogen-Activated Protein KinasesPhosphorylationPlectinPodocytesRatsActinsDoxorubicinFocal Adhesion Kinase 1Integrin alpha6beta4p38 Mitogen-Activated Protein KinasesPlectinPtk2 protein, mouseapoptosisF-actin cytoskeletonFAKintegrin α6β4p38 MAPK pathwayplectinpodocyte

Identifiers

PMID30187999
PMCPMC6201223
OpenAlexW2890979948

What OpenQuestion 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 OpenQuestion graph.