Evidence map›Paper›PMID 35159350›Full record

ArticleCells2022

Dynamic Spatiotemporal Expression Pattern of the Senescence-Associated Factor p16Ink4a in Development and Aging.

Hasan Safwan-Zaiter, Nicole Wagner, Jean-François Michiels, Kay-Dietrich Wagner

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Cerebrovascular p16Acta neuropathologica communications · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Cellular senescence and kidney aging.Clinical science (London, England : 1979) · 2023
    Review
  15. Time- and Gender-Dependent Alterations in Mice during the Aging Process.International journal of molecular sciences · 2023
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  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 at 2 institutions in 1 country.

Hasan Safwan-ZaiterThe National Center for Scientific Research (CNRS), The National Institute of Health and Medical Research (INSERM), iBV, Université Côte d'Azur, 06107 Nice, France.
Nicole WagnerThe National Center for Scientific Research (CNRS), The National Institute of Health and Medical Research (INSERM), iBV, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0002-2746-0707
Jean-François MichielsDepartment of Pathology, CHU Nice, 06107 Nice, France.
Kay-Dietrich WagnerThe National Center for Scientific Research (CNRS), The National Institute of Health and Medical Research (INSERM), iBV, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0001-5483-7760
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Nice · FR

Funding

Agence Nationale de la Recherche R19125AACSRD VA 1Fondation ARC pour la Recherche sur le Cancer PJA 20161204650Fondation pour la Recherche Médicale DPC20170139474
6 · The paper itself

Abstract

A plethora of factors have been attributed to underly aging, including oxidative stress, telomere shortening and cellular senescence. Several studies have shown a significant role of the cyclin-dependent kinase inhibitor p16ink4a in senescence and aging. However, its expression in development has been less well documented. Therefore, to further clarify a potential role of p16 in development and aging, we conducted a developmental expression study of p16, as well as of p19ARF and p21, and investigated their expression on the RNA level in brain, heart, liver, and kidney of mice at embryonic, postnatal, adult, and old ages. P16 expression was further assessed on the protein level by immunohistochemistry. Expression of p16 was highly dynamic in all organs in embryonic and postnatal stages and increased dramatically in old mice. Expression of p19 and p21 was less variable and increased to a moderate extent at old age. In addition, we observed a predominant expression of p16 mRNA and protein in liver endothelial cells versus non-endothelial cells of old mice, which suggests a functional role specifically in liver endothelium of old subjects. Thus, p16 dynamic spatiotemporal expression might implicate p16 in developmental and physiological processes in addition to its well-known function in the build-up of senescence.

Indexed as

Cyclin-Dependent Kinase Inhibitor p16Endothelial CellsAgingAnimalsCellular SenescenceHumansMiceRNA, MessengerCyclin-Dependent Kinase Inhibitor p16RNA, Messengeragingbraindevelopmentendothelial cellsheartkidneyliverSASPsenescence

Identifiers

PMID35159350
PMCPMC8833900
OpenAlexW4210266553

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.