Evidence map›Paper›PMID 38641866›Full record

ReviewCancer science2024

Senescence and senolysis in cancer: The latest findings.

Yoshimi Imawari, Makoto Nakanishi

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  4. Unleashing endogenous regeneration by senolytics.Journal of translational medicine · 2025
    Review
  5. Article
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  7. Article
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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

2 authors at 2 institutions in 1 country.

Yoshimi ImawariDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5754-1818
Makoto NakanishiDivision of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6707-3584
Jikei University School of Medicine · JPTokyo University of Science · JP

Funding

Japan Agency for Medical Research and Development JP20ck010655hJapan Agency for Medical Research and Development JP20gm5010001sJapan Agency for Medical Research and Development JP23gm1410013hJapan Agency for Medical Research and Development JP23zf0127003hJapan Science and Technology Agency JP19H05740Japan Science and Technology Agency JP20H00514Japan Science and Technology Agency JP20K21497Japan Science and Technology Agency JP21K16408
6 · The paper itself

Abstract

Aging is a life phenomenon that occurs in most living organisms and is a major risk factor for many diseases, including cancer. Cellular senescence is a cellular trait induced by various genomic and epigenetic stresses. Senescent cells are characterized by irreversible cell growth arrest and excessive secretion of inflammatory cytokines (senescence-associated secretory phenotypes, SASP). Chronic tissue microinflammation induced by SASP contributes to the pathogenesis of a variety of age-related diseases, including cancer. Senolysis is a promising new strategy to selectively eliminate senescent cells in order to suppress chronic inflammation, suggesting its potential use as an anticancer therapy. This review summarizes recent findings on the molecular basis of senescence in cancer cells and senolysis.

Indexed as

Cellular SenescenceNeoplasmsSenescence-Associated Secretory PhenotypeAgingAnimalsCytokinesHumansInflammationCytokinesagingcancerGLS1senescencesenolysis

Identifiers

PMID38641866
PMCPMC11247613
OpenAlexW4394981483

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.