Evidence map›Paper›PMID 33014273›Full record

ReviewOxidative medicine and cellular longevity2020

The Role of BRG1 in Antioxidant and Redox Signaling.

Shilong You, Ying Zhang, Jiaqi Xu, Hao Qian, Shaojun Wu, Boquan Wu, Saien Lu, Yingxian Sun, Naijin Zhang

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Promotion of DFU Wound Healing via BRG1-COL16A1 Axis in Fibroblasts.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Dancr-BRG1 regulates Nfatc1 transcription and Pgc1β-dependent metabolic shifts in osteoclastogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

9 authors at 1 institution in 1 country.

Shilong YouDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Ying ZhangDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Jiaqi XuDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Hao QianDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Shaojun WuDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Boquan WuDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Saien LuDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Yingxian SunDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0002-1961-899X
Naijin ZhangDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0003-3653-9801
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Redox homeostasis is regulated by critical molecules that modulate antioxidant and redox signaling (ARS) within the cell. Imbalances among these molecules can lead to oxidative stress and damage to cell functions, causing a variety of diseases. Brahma-related gene 1 (BRG1), also known as SMARCA4, is the central ATPase catalytic subunit of the switch/sucrose nonfermentable (SWI/SNF) chromatin remodeling complex, which plays a core role in DNA replication, repair, recombination, and transcriptional regulation. Numerous recent studies show that BRG1 is involved in the regulation of various cellular processes associated with ARS. BRG1, as a major factor in chromatin remodeling, is essential for the repair of oxidative stress-induced DNA damage and the activation of antioxidant genes under oxidative stress. Consequently, a comprehensive understanding of the roles of BRG1 in redox homeostasis is crucial to understand the normal functioning as well as pathological mechanisms. In this review, we summarized and discussed the role of BRG1 in the regulation of ARS.

Indexed as

Signal TransductionAntioxidantsDNA HelicasesHumansMicroRNAsNF-E2-Related Factor 2NF-kappa BNuclear ProteinsOxidative StressReactive Oxygen SpeciesTranscription FactorsTumor Suppressor Protein p53AntioxidantsDNA HelicasesMicroRNAsNF-E2-Related Factor 2NF-kappa BNuclear ProteinsReactive Oxygen SpeciesSMARCA4 protein, humanTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID33014273
PMCPMC7512085
OpenAlexW3085047984

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.