Evidence map›Paper›PMID 32936311›Full record

ReviewCellular and molecular life sciences : CMLS2021

Induction and transmission of oncogene-induced senescence.

Nattaphong Rattanavirotkul, Kristina Kirschner, Tamir Chandra

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Review
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  10. Review
  11. Review
  12. Dissecting the Heterogeneity of Senescent Cells Through CITE-seq Integration.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  13. Isolation and Characterization of EVs Containing Mitochondria from OIS Cells.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  14. Review
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  17. 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

3 authors.

Nattaphong RattanavirotkulChakri Naruebodindra Medical Institute, Ramathibodi Medical School, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 111, Bang Pla, Bang Phli, Samut Prakan, 10540, Thailand. nattaphong.rat@mahidol.ac.th.
Kristina KirschnerInstitute of Cancer Sciences, University of Glasgow, Glasgow, G61 1BD, UK. kristina.kirschner@glasgow.ac.uk.
Tamir ChandraMRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, The University of Edinburgh, Edinburgh, UK. tamir.chandra@igmm.ed.ac.uk.ORCID http://orcid.org/0000-0002-7935-317X

Funding

College of Medicine and Veterinary Medicine, University of Edinburgh Chancellor's FellowshipJohn Goldman Fellowship 2019/JGF/003Wellcome Trust 206194
6 · The paper itself

Abstract

Senescence is a cellular stress response triggered by diverse stressors, including oncogene activation, where it serves as a bona-fide tumour suppressor mechanism. Senescence can be transmitted to neighbouring cells, known as paracrine secondary senescence. Secondary senescence was initially described as a paracrine mechanism, but recent evidence suggests a more complex scenario involving juxtacrine communication between cells. In addition, single-cell studies described differences between primary and secondary senescent end-points, which have thus far not been considered functionally distinct. Here we discuss emerging concepts in senescence transmission and heterogeneity in primary and secondary senescence on a cellular and organ level.

Indexed as

AnimalsCCAAT-Enhancer-Binding Protein-betaCellular SenescenceHumansJagged-1 ProteinOncogenesParacrine CommunicationReceptors, NotchSignal TransductionTransforming Growth Factor betaCCAAT-Enhancer-Binding Protein-betaJagged-1 ProteinReceptors, NotchTransforming Growth Factor betaJuxtacrine senescenceNotch signallingOncogene-induced senescenceSecondary senescence

Identifiers

PMID32936311
PMCPMC7897614

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.