Evidence map›Paper›PMID 25855157›Full record

ReviewThe Journal of investigative dermatology2015

Cell Autonomous and Non-Autonomous Effects of Senescent Cells in the Skin.

Marco Demaria, Pierre Yves Desprez, Judith Campisi, Michael C Velarde

Abstract readReview
In one paragraph

Review in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing 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

59 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
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  8. Article
  9. Topical Application of miR-200b-3p by Poloxamer 407-Based Hydrogel Accelerates Diabetic Wound Healing.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. [Skin aging-cellular senescence : What is the future?]Dermatologie (Heidelberg, Germany) · 2023
    Review
  20. Article
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.

Marco DemariaCampisi Laboratory, Buck Institute for Research on Aging, Novato, California, USA.
Pierre Yves DesprezCampisi Laboratory, Buck Institute for Research on Aging, Novato, California, USA; California Pacific Medical Center Research Institute, San Francisco, California, USA.
Judith CampisiCampisi Laboratory, Buck Institute for Research on Aging, Novato, California, USA; Lawrence Berkley National Laboratory, Life Sciences Division, Berkeley, California, USA.
Michael C VelardeCampisi Laboratory, Buck Institute for Research on Aging, Novato, California, USA. Electronic address: mvelarde@buckinstitute.org.

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
Systems Biology and Bioinformatics CoreP01AG041122 · NIA · MAYO CLINIC ROCHESTER · PI CAMPISI, JUDITH · 2012 to 2016
$9.8M
CELLULAR SENESCENCE AND CONTROL OF GENE EXPRESSIONR37AG009909 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CAMPISI, JUDITH · 1995 to 2015
$7.6M
The role of senescent cells in late-life tumorigenesisR01CA166347 · NCI · MAYO CLINIC ROCHESTER · PI VAN DEURSEN, JAN M. · 2013 to 2017
$1.7M
Montagna Symposium on the Biology of SkinR13AR009431 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI SANCY ANN LEACHMAN · 1986 to 2026
$785k
Role of Mitochondria in Estrogen Action and Cellular SenescenceK99AG041221 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI VELARDE, MICHAEL C. · 2012 to 2013
$180k
NCI NIH HHS R01 CA166347NCI NIH HHS R21-CA166347NIAMS NIH HHS R13 AR009431NIA NIH HHS K99 AG041221NIA NIH HHS K99-AG041221NIA NIH HHS P01 AG017242NIA NIH HHS P01- AG017242NIA NIH HHS P01 AG041122NIA NIH HHS P01-AG041122NIA NIH HHS R37 AG009909NIA NIH HHS R37-AG009909
6 · The paper itself

Abstract

Human and mouse skin accumulate senescent cells in both the epidermis and dermis during aging. When chronically present, senescent cells are thought to enhance the age-dependent deterioration of the skin during extrinsic and intrinsic aging. However, when transiently present, senescent cells promote optimal wound healing. Here, we review recent studies on how senescent cells and the senescence-associated secretory phenotype contribute to different physiological and pathophysiological conditions in the skin with a focus on some of the cell autonomous and non-autonomous functions of senescent cells in the context of skin aging and wound healing.

Indexed as

Epidermal CellsAnimalsCell DifferentiationCell DivisionCellular SenescenceEpidermisFemaleFibroblastsHomeostasisHumansMaleMiceSensitivity and SpecificitySkinSkin AgingWound Healing

Identifiers

PMID25855157
PMCPMC4466004

What OpenQuestion holds

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LicenceTDM
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.