Evidence map›Paper›PMID 36253355›Full record

ReviewCell death discovery2022

Cellular senescence in ischemia/reperfusion injury.

Chaojin Chen, Muxu Zheng, Hongbiao Hou, Sijian Fang, Liubing Chen, Jing Yang, Weifeng Yao, Qi Zhang, Ziqing Hei

Abstract readReview
In one paragraph

Review in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
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  7. Integrating senotherapeutics into transplantation: liver reconditioning in an aging donor pool.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    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

9 authors.

Chaojin Chen *Department of Anesthesiology, The Third Affiliated Hospital of Sun Yat‑sen University, 510630, Guangzhou, Guangdong, P. R. China.
Muxu Zheng *School of Medicine, Sun Yat-sen University, 518107, Shenzhen, Guangdong, P. R. China.
Hongbiao HouSchool of Medicine, Sun Yat-sen University, 518107, Shenzhen, Guangdong, P. R. China.
Sijian FangSchool of Medicine, Sun Yat-sen University, 518107, Shenzhen, Guangdong, P. R. China.
Liubing ChenDepartment of Anesthesiology, The Third Affiliated Hospital of Sun Yat‑sen University, 510630, Guangzhou, Guangdong, P. R. China.
Jing YangDepartment of Anesthesiology, The Third Affiliated Hospital of Sun Yat‑sen University, 510630, Guangzhou, Guangdong, P. R. China.
Weifeng YaoDepartment of Anesthesiology, The Third Affiliated Hospital of Sun Yat‑sen University, 510630, Guangzhou, Guangdong, P. R. China. yaowf3@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-5284-9159
Qi ZhangCell-gene Therapy Translational Medicine Research Center, The Third Affiliated Hospital of Sun Yat-sen University, 510630, Guangzhou, Guangdong, P. R. China. zhangq27@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-9916-8919
Ziqing HeiDepartment of Anesthesiology, The Third Affiliated Hospital of Sun Yat‑sen University, 510630, Guangzhou, Guangdong, P. R. China. heiziqing@sina.com.ORCID http://orcid.org/0000-0001-7466-2769

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81974296National Natural Science Foundation of China (National Science Foundation of China) 82102297Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2019A1515110020Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2022A1515012603
6 · The paper itself

Abstract

Ischemia/reperfusion (IR) injury, a main reason of mortality and morbidity worldwide, occurs in many organs and tissues. As a result of IR injury, senescent cells can accumulate in multiple organs. Increasing evidence shows that cellular senescence is the underlying mechanism that transforms an acute organ injury into a chronic one. Several recent studies suggest senescent cells can be targeted for the prevention or elimination of acute and chronic organ injury induced by IR. In this review, we concisely introduce the underlying mechanism and the pivotal role of premature senescence in the transition from acute to chronic IR injuries. Special focus is laid on recent advances in the mechanisms as well as on the basic and clinical research, targeting cellular senescence in multi-organ IR injuries. Besides, the potential directions in this field are discussed in the end. Together, the recent advances reviewed here will act as a comprehensive overview of the roles of cellular senescence in IR injury, which could be of great significance for the design of related studies, or as a guide for potential therapeutic target.

Identifiers

PMID36253355
PMCPMC9576687

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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.