Evidence map›Paper›PMID 33328614›Full record

ReviewNature reviews. Molecular cell biology2021

Cellular senescence in ageing: from mechanisms to therapeutic opportunities.

Raffaella Di Micco, Valery Krizhanovsky, Darren Baker, Fabrizio d'Adda di Fagagna

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05637216 (A Pilot Study of Losartan to Reduce Radiation Induced Fibrosis in Breast Cancer Patients), which is not on this map. Cited by 1,317 papers.

0numbers the graph read from it
0cells of the map it votes in
1,317citing papers in PubMed
99.0field-weighted citation impact, top 1% 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.

NCT05637216 phase2active not recruitingnot on this mapstarted 2023, after this paper: background citation

A Pilot Study of Losartan to Reduce Radiation Induced Fibrosis in Breast Cancer Patients

TypeinterventionalSponsorShaw Cancer CenterRan2023 to 2027Enrolled43ConditionsRadiation Induced FibrosisArmsLosartan 25 milligram capsule, Placebo
3 · Its place in the literature

Who cites it

1,317 citing papers in PubMed, 2,076 citations in OpenAlex.

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  13. PP4 deficiency drives airway epithelial senescence via the PERK-eIF2α-ATF4-p21 axis in severe asthma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  14. Article
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  16. Terpenoids as modulators of autophagy-senescence crosstalk in lung cancer.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2026
    Review
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  19. Article
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1,257 more citing papers are in PubMed but not listed here.

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

4 authors at 4 institutions in 3 countries.

Raffaella Di MiccoSan Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, Milan, Italy. dimicco.raffaella@hsr.it.ORCID http://orcid.org/0000-0002-0639-8238
Valery KrizhanovskyDepartment of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0002-3977-5482
Darren BakerDepartment of Pediatrics, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-9006-1939
Fabrizio d'Adda di FagagnaIFOM - The FIRC Institute of Molecular Oncology, Milan, Italy. fabrizio.dadda@ifom.eu.ORCID http://orcid.org/0000-0002-9603-5966
IFOM · ITMayo Clinic in Arizona · USThe San Raffaele Telethon Institute for Gene Therapy · ITWeizmann Institute of Science · IL

Funding

The contribution of p16-expressing cells to tauopathyR01AG053229 · NIA · MAYO CLINIC ROCHESTER · PI BAKER, DARREN · 2017 to 2021
$2.0M
Effects of senescence to Alzheimer's disease pathologyR01AG068076 · NIA · MAYO CLINIC ROCHESTER · PI BAKER, DARREN · 2020 to 2024
$2.0M
NIA NIH HHS R01 AG053229NIA NIH HHS R01 AG068076
6 · The paper itself

Abstract

Cellular senescence, first described in vitro in 1961, has become a focus for biotech companies that target it to ameliorate a variety of human conditions. Eminently characterized by a permanent proliferation arrest, cellular senescence occurs in response to endogenous and exogenous stresses, including telomere dysfunction, oncogene activation and persistent DNA damage. Cellular senescence can also be a controlled programme occurring in diverse biological processes, including embryonic development. Senescent cell extrinsic activities, broadly related to the activation of a senescence-associated secretory phenotype, amplify the impact of cell-intrinsic proliferative arrest and contribute to impaired tissue regeneration, chronic age-associated diseases and organismal ageing. This Review discusses the mechanisms and modulators of cellular senescence establishment and induction of a senescence-associated secretory phenotype, and provides an overview of cellular senescence as an emerging opportunity to intervene through senolytic and senomorphic therapies in ageing and ageing-associated diseases.

Indexed as

AgingCellular SenescenceTelomereTranslational Research, BiomedicalAnimalsCell ProliferationDNA DamageHumansPhenotype

Identifiers

PMID33328614
PMCPMC8344376
OpenAlexW3111207111

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.