Evidence map›Paper›PMID 22158419›Full record

ReviewCell death and differentiation2012

Regulation of skin aging and heart development by TAp63.

M Paris, M Rouleau, M Pucéat, D Aberdam

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 54 citations in OpenAlex.

  1. Conversion from twice-daily tacrolimus to once-daily extended release tacrolimus (LCPT): the phase III randomized MELT trial.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2013
    Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. A scATAC-seq atlas of stasis zone in rat skin burn injury wound process.Frontiers in cell and developmental biology · 2024
    Article
  7. The dual role of p63 in cancer.Frontiers in oncology · 2023
    Review
  8. Structural diversity of p63 and p73 isoforms.Cell death and differentiation · 2022
    Review
  9. The Impact of Vitamin D on Skin Aging.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Silencing or not silencingJournal of thoracic disease · 2018
    Article
  12. Article
  13. DNA replication timing alterations identify common markers between distinct progeroid diseases.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Sequence variation inEMBO molecular medicine · 2017
    Article
  15. How Does p73 Cause Neuronal Defects?Molecular neurobiology · 2016
    Review
  16. Article
  17. The function of Drosophila p53 isoforms in apoptosis.Cell death and differentiation · 2015
    Article
  18. p63 supports aerobic respiration through hexokinase II.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  19. Article
  20. TAp73 promotes anabolism.Oncotarget · 2014
    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 3 institutions in 1 country.

M ParisL'OREAL Recherche, Clichy, France.
M Rouleau
M Pucéat
D Aberdam
Inserm · FRDélégation Paris 5 · FRL'Oréal (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the discovery of the TP63 gene in 1998, many studies have demonstrated that ΔNp63, a p63 isoform of the p53 gene family, is involved in multiple functions during skin development and in adult stem/progenitor cell regulation. In contrast, TAp63 studies have been mostly restricted to its apoptotic function and more recently as the guardian of oocyte integrity. TAp63 endogenous expression is barely detectable in embryos and adult (except in oocytes), presumably because of its rapid degradation and the lack of antibodies able to detect weak expression. Nevertheless, two recent independent studies have demonstrated novel functions for TAp63 that could have potential implications to human pathologies. The first discovery is related to the protective role of TAp63 on premature aging. TAp63 controls skin homeostasis by maintaining dermal and epidermal progenitor/stem cell pool and protecting them from senescence, DNA damage and genomic instability. The second study is related to the role of TAp63, expressed by the primitive endoderm, on heart development. This unexpected role for TAp63 has been discovered by manipulation of embryonic stem cells in vitro and confirmed by the severe cardiomyopathy observed in brdm2 p63-null embryonic hearts. Interestingly, in both cases, TAp63 acts in a cell-nonautonomous manner on adjacent cells. Here, we discuss these findings and their potential connection during development.

Indexed as

AnimalsCell LineageEpitheliumHeartHumansSkin AgingTumor Suppressor ProteinsTumor Suppressor Proteins

Identifiers

PMID22158419
PMCPMC3263495
OpenAlexW2033287052

What OpenQuestion holds

Textmetadata
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.