Evidence map›Paper›PMID 27888193›Full record

ArticleDevelopment (Cambridge, England)2017

Conserved and novel functions of programmed cellular senescence during vertebrate development.

Hongorzul Davaapil, Jeremy P Brockes, Maximina H Yun

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 119 citations in OpenAlex.

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  14. Emerging role of cellular senescence in normal lung development and perinatal lung injury.Chinese medical journal pulmonary and critical care medicine · 2024
    Article
  15. Review
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  17. Article
  18. Dietary restriction in senolysis and prevention and treatment of disease.Critical reviews in food science and nutrition · 2024
    Review
  19. Review
  20. Review

10 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

3 authors at 1 institution in 1 country.

Hongorzul DavaapilInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, London WC1E 6BT, UK.
Jeremy P BrockesInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, London WC1E 6BT, UK.
Maximina H YunInstitute of Structural and Molecular Biology, Division of Biosciences, University College London, London WC1E 6BT, UK maximina.yun@ucl.ac.uk.ORCID 0000-0001-9019-2453
Institute of Structural and Molecular Biology · GB

Funding

Medical Research Council G0701297Medical Research Council G1000870Wellcome Trust
6 · The paper itself

Abstract

Cellular senescence, a form of stable cell cycle arrest that is traditionally associated with tumour suppression, has been recently found to occur during mammalian development. Here, we show that cell senescence is an intrinsic part of the developmental programme in amphibians. Programmed senescence occurs in specific structures during defined time windows during amphibian development. It contributes to the physiological degeneration of the amphibian pronephros and to the development of the cement gland and oral cavity. In both contexts, senescence depends on TGFβ but is independent of ERK/MAPK activation. Furthermore, elimination of senescent cells through temporary TGFβ inhibition leads to developmental defects. Our findings uncover conserved and new roles of senescence in vertebrate organogenesis and support the view that cellular senescence may have arisen in evolution as a developmental mechanism.

Indexed as

Ambystoma mexicanumAmphibiansAnimalsApoptosis Regulatory ProteinsCellular SenescenceEmbryonic DevelopmentEmbryo, NonmammalianKidneyOrganogenesisTransforming Growth Factor betaVertebratesXenopus laevisApoptosis Regulatory ProteinsTransforming Growth Factor betaAxolotlCellular senescenceCement glandKidneyTGFβXenopus

Identifiers

PMID27888193
PMCPMC5278627
OpenAlexW2555998158

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.