Evidence map›Paper›PMID 37059928›Full record

ArticleNeurochemical research2023

GATA6 Inhibits Neuronal Autophagy and Ferroptosis in Cerebral ischemia-reperfusion Injury Through a miR-193b/ATG7 axis-dependent Mechanism.

Weijian Fan, Jianjie Rong, Weihao Shi, Wei Liu, Jie Wang, Jinyun Tan, Bo Yu, Jindong Tong

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. 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

8 authors at 4 institutions in 1 country.

Weijian FanDepartment of Vascular Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong, Shanghai, 201300, P. R. China.
Jianjie RongDepartment of Vascular Surgery, Suzhou TCM Hospital, Nanjing University of Chinese Medicine, Suzhou215000, Nanjing, P.R. China.
Weihao ShiDepartment of Vascular Surgery, Huashan Hospital of Fudan University, No.12, Mid-Wulumuqi Road, Shanghai, 200040, P.R. China.
Wei LiuDepartment of Neurology, Suzhou TCM Hospital, Nanjing University of Chinese Medicine, Suzhou215000, Nanjing, P.R. China.
Jie WangDepartment of Vascular Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong, Shanghai, 201300, P. R. China.
Jinyun TanDepartment of Vascular Surgery, Huashan Hospital of Fudan University, No.12, Mid-Wulumuqi Road, Shanghai, 200040, P.R. China.
Bo YuDepartment of Vascular Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong, Shanghai, 201300, P. R. China. paul.yubo@gmail.com.
Jindong TongDepartment of Vascular Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong, Shanghai, 201300, P. R. China. jindong1220@163.com.
Fudan University · CNHuashan Hospital · CNNanjing University of Chinese Medicine · CNPudong Medical Center · CN

Funding

Program for Medical Key subspecialty Department of Shanghai Pudong health system PWZy2020-13Pudong New Area Clinical Plateau Discipline Project PWYgy2021-03Science and Technology Commission of Shanghai Municipality 20Y11909700the Science and Technology Project of Suzhou City of China No. SYS2019106, SYS2020186, SKY2021011the Seventh Batch of Health Personnel Training Project in Suzhou No. GSWS2020083
6 · The paper itself

Abstract

Ferroptosis is a newly described form of regulated necrotic cell death, which is engaged in the pathological cell death related to stroke, contributing to cerebral ischemia-reperfusion (I/R) injury. Therefore, we performed this study to clarify the role of GATA6 in neuronal autophagy and ferroptosis in cerebral I/R injury. The cerebral I/R injury-related differentially expressed genes (DEGs) as well as the downstream factors of GATA6 were predicted bioinformatically. Moreover, the relations between GATA6 and miR-193b and that between miR-193b and ATG7 were evaluated by chromatin immunoprecipitation and dual-luciferase reporter assays. Besides, neurons were treated with oxygen-glucose deprivation (OGD), followed by overexpression of GATA6, miR-193b, and ATG7 alone or in combination to assess neuronal autophagy and ferroptosis. At last, in vivo experiments were performed to explore the impacts of GATA6/miR-193b/ATG7 on neuronal autophagy and ferroptosis in a rat model of middle cerebral artery occlusion (MCAO)-stimulated cerebral I/R injury. It was found that GATA6 and miR-193b were poorly expressed in cerebral I/R injury. GATA6 transcriptionally activated miR-193b to downregulate ATG7. Additionally, GATA6-mediated miR-193b activation suppressed neuronal autophagy and ferroptosis in OGD-treated neurons by inhibiting ATG7. Furthermore, GATA6/miR-193b relieved cerebral I/R injury by restraining neuronal autophagy and ferroptosis via downregulation of ATG7 in vivo. In summary, GATA6 might prevent neuronal autophagy and ferroptosis to alleviate cerebral I/R injury via the miR-193b/ATG7 axis.

Indexed as

Autophagy-Related Protein 7GATA6 Transcription FactorInfarction, Middle Cerebral ArteryMicroRNAsAnimalsAutophagyBrainDisease Models, AnimalFerroptosisGene Regulatory NetworksMaleNeuronsRatsRats, Sprague-DawleyReperfusion InjuryUp-RegulationAtg7 protein, ratAutophagy-Related Protein 7Gata6 protein, ratGATA6 Transcription FactorMicroRNAsMirn193 microRNA, ratATG7Cerebral ischemia-reperfusion injuryFerroptosisGATA6microRNA-193bNeuronal autophagy

Identifiers

PMID37059928
OpenAlexW4365810915

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.