Evidence map›Paper›PMID 34539989›Full record

ArticleAmerican journal of translational research2021

CircUBXN7 mitigates H/R-induced cell apoptosis and inflammatory response through the miR-622-MCL1 axis.

Sheng Wang, Zhaoyun Cheng, Xianjie Chen, Guoqing Lu, Xiliang Zhu, Gaojun Xu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2021. 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
1.5field-weighted citation impact, top 18% 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, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Role of ncRNAs in Cardiac Infarction and Regeneration.Journal of cardiovascular development and disease · 2023
    Review
  8. Review
  9. Circular RNAs in organ injury: recent development.Journal of translational medicine · 2022
    Review
  10. Review
  11. Article
  12. Article
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  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

6 authors at 1 institution in 1 country.

Sheng WangDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Zhaoyun ChengDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Xianjie ChenDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Guoqing LuDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Xiliang ZhuDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Gaojun XuDepartment of Cardiovascular Surgery, Fuwai Central China Cardiovascular Hospital, Heart Center of He'nan Provincial People's Hospital Zhengzhou, He'nan Province, China.
Zhengzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxia/reoxygenation (H/R)-mediated apoptosis and inflammation are major causes of tissue injury in acute myocardial infarction (AMI). Exploring the underlying mechanisms of cardiomyocyte injury induced by H/R is important for AMI treatment. Circular RNAs have been demonstrated to paly vital roles in the pathogenesis of AMI. Our study aimed to explore the function of circular RNA UBXN7 (circUBXN7) in regulating H/R-induced cardiomyocyte injury.

methodsH/R-treated H9c2 cells and a mouse model of AMI were used to investigate the function of circUBXN7 in H/R damage and AMI. The expressions of circUNXN7, miR-622 and MCL1 were analyzed by RT-qPCR. CCK-8 was used for examining cell viability. Cell apoptosis was evaluated with caspase 3 activity and Annexin V/PI staining. MCL1, Bax, Bcl-2 and cleaved-caspase 3 were examined with western blot. ELISA was used to examine the secretion of IL-6, TNF-α and IL-1β.

resultsCircUBXN7 was downregulated in patients and mice with AMI, as well as in H/R-treated cells. Overexpression of circUBXN7 mitigated H/R-mediated apoptosis and secretion of inflammatory factors including IL-6, TNF-α and IL-1β. CircUBXN7 suppressed cell apoptosis and inflammatory reaction induced by H/R via targeting miR-622. MiR-622 targeted MCL1 to restrain its expression in H9c2 cells. Knockdown of MCL1 abrogated circUBXN7-mediated alleviation of apoptosis and inflammation after H/R treatment.

conclusionCircUBXN7 mitigates cardiomyocyte apoptosis and inflammatory reaction in H/R injury by targeting miR-622 and maintaining MCL1 expression. Our study provides novel potential therapeutic targets for AMI treatment.

Indexed as

apoptosiscircular RNA UBXN7hypoxia/reoxygenationinflammatory responsemiR-622-MCL1 axis

Identifiers

PMID34539989
PMCPMC8430130
OpenAlexW3199803359

What OpenQuestion holds

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Registered trials

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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.