Evidence map›Paper›PMID 36685533›Full record

ArticleFrontiers in immunology2022

m6A eraser FTO modulates autophagy by targeting SQSTM1/P62 in the prevention of canagliflozin against renal fibrosis.

Youjing Yang, Qianmin Li, Yi Ling, Linxin Leng, Yu Ma, Lian Xue, Guoyuan Lu, Yue Ding, Jianzhong Li, Shasha Tao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  10. Decoding mJournal of translational medicine · 2025
    Review
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  12. MAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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  18. m6A demethylase FTO transcriptionally activated by SP1 improves ischemia reperfusion-triggered acute kidney injury by activating Ambra1/ULK1-mediated autophagy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  19. Review
  20. Sodium-glucose cotransporter-2 inhibitors protect tissuesWorld journal of experimental medicine · 2024
    Review
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 4 institutions in 1 country.

Youjing YangChongqing University Central Hospital and Chongqing Emergency Medical Center, Chongqing, China.
Qianmin LiSchool of Public Health, Medical College of Soochow University, Suzhou, China.
Yi LingSchool of Public Health, Medical College of Soochow University, Suzhou, China.
Linxin LengSchool of Public Health, Medical College of Soochow University, Suzhou, China.
Yu MaChongqing University Central Hospital and Chongqing Emergency Medical Center, Chongqing, China.
Lian XueSchool of Public Health, Medical College of Soochow University, Suzhou, China.
Guoyuan LuDepartment of Nephrology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yue DingDepartment of Nephrology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Jianzhong LiDepartment of Nephrology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Shasha TaoChongqing University Central Hospital and Chongqing Emergency Medical Center, Chongqing, China.
Soochow University · CNChongqing Emergency Medical Center · CNChongqing University · CNFirst Affiliated Hospital of Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dysregulation of autophagy contributes to renal fibrosis. N6-Methyladenosine (m6A) RNA modification is a critical mediator of autophagy. Our previous studies have reported that the disorder of the PPARα/fatty acid oxidation (FAO) axis in renal tubular cells is suppressed by STAT6, which is involved in the regulation of renal fibrotic processes. Here, we found that canagliflozin significantly upregulates SQSTM1/P62, promoting PPARα-mediated FAO by inducing autophagy-dependent STAT6 degradation both in TGF-β1-treated HK2 cells and in unilateral ureteral occlusion (UUO) and ischemia-reperfusion (I/R) renal fibrosis mouse models. Knockdown of P62/SQSTM1 led to the impairment autophagic flux and the dysregulation of the STAT6/PPARα axis, which was confirmed by SQSTM1/P62

Indexed as

Kidney DiseasesUreteral ObstructionAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsAutophagyCanagliflozinFibrosisMicePPAR alphaRNA, MessengerSequestosome-1 ProteinAlpha-Ketoglutarate-Dependent Dioxygenase FTOCanagliflozinFTO protein, mousePPAR alphaRNA, MessengerSequestosome-1 ProteinSqstm1 protein, mouseautophagycanagliflozinN6-methyladenosinerenal fibrosisSQSTM1STAT6

Identifiers

PMID36685533
PMCPMC9845768
OpenAlexW4313470818

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.