Evidence map›Paper›PMID 39909458›Full record

ReviewZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences2025

[Mechanism and significance of cell senescence induced by viral infection].

Yunchuang Chang, Xinna Wu, Lingli Deng, Sanying Wang, Genxiang Mao

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Yunchuang ChangCollege of Biological and Food Engineering, Hubei Minzu University, Enshi 445000, Hubei Province, China. cyc147927@163.com.
Xinna WuZhejiang University School of Medicine, Hangzhou 310058, China.
Lingli DengCollege of Biological and Food Engineering, Hubei Minzu University, Enshi 445000, Hubei Province, China.
Sanying WangZhejiang Provincial Geriatrics Institute, Zhejiang Key Laboratory of Geriatrics, Zhejiang Hospital, Hangzhou 310030, China. sanyingwang309@126.com.
Genxiang MaoCollege of Biological and Food Engineering, Hubei Minzu University, Enshi 445000, Hubei Province, China. maogenxiang@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus-induced senescence (VIS) is a significant biological phenomenon, which is associated with declining immune function, accelerating aging process and causing aging-related diseases. A variety of common viruses, including RNA viruses (such as SARS-CoV-2), DNA viruses (such as herpesviruses and hepatitis B virus), and prions can cause VIS in host cells. The primary mechanisms include abnormal activation of the cGAS-STING signaling pathway, DNA damage response, and potential correlations with the integrated stress response due to intracellular phase separation. Viral infection and cellular senescence influence each other: cellular senescence serves as a defense to restrict viral replication and transmission, while some viruses exploit cellular senescence to enhance their infectivity and replication. Understanding the mechanisms of VIS is conducive to the development of therapeutic strategies for viral infections and promotion of healthy aging. However, there is lack of research on therapeutic targets and drug development in this field so far. Although senolytics may be effective for anti-senescent cells therapy, their efficacy for VIS needs evidence from further clinical trials. This article reviews the research progress on the connection between viral infection and cellular senescence, to provide insights for the prevention and treatment of aging related diseases.

Indexed as

Cellular SenescenceVirus DiseasesCOVID-19Cyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNA DamageHumansMembrane ProteinsNucleotidyltransferasesSARS-CoV-2Signal TransductionSTING ProteinVirus ReplicationcGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesSTING1 protein, humanSTING ProteinCell senescencecGAS-STINGDNA damage responseReviewViral infection

Identifiers

PMID39909458
PMCPMC11956860

What OpenQuestion holds

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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.