Evidence map›Paper›PMID 19718028›Full record

ArticleNature genetics2009

p53 deletion impairs clearance of chromosomal-instable stem cells in aging telomere-dysfunctional mice.

Yvonne Begus-Nahrmann, André Lechel, Anna C Obenauf, Kodandaramireddy Nalapareddy, Elvira Peit, Eva Hoffmann, Falk Schlaudraff, Birgit Liss, Peter Schirmacher, Hans Kestler and 5 more

Abstract read
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In one paragraph

Article in Nature genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Aging and Altered Gravity: A Cellular Perspective.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. p53 balances between tissue hierarchy and anarchy.Journal of molecular cell biology · 2019
    Review
  18. Article
  19. Mitophagy-driven metabolic switch reprograms stem cell fate.Cellular and molecular life sciences : CMLS · 2019
    Review
  20. Article

3 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

15 authors at 4 institutions in 3 countries.

Yvonne Begus-NahrmannInstitute of Molecular Medicine and Max-Planck-Research Department on Stem Cell Aging, University of Ulm, Ulm, Germany.
André Lechel
Anna C Obenauf
Kodandaramireddy Nalapareddy
Elvira Peit
Eva Hoffmann
Falk Schlaudraff
Birgit Liss
Peter Schirmacher
Hans Kestler
Esther Danenberg
Nick Barker
Hans Clevers
Michael R Speicher
K Lenhard Rudolph
Universität Ulm · DEHubrecht Institute for Developmental Biology and Stem Cell Research · NLMedical University of Graz · ATUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomere dysfunction limits the proliferative capacity of human cells and induces organismal aging by activation of p53 and p21. Although deletion of p21 elongates the lifespan of telomere-dysfunctional mice, a direct analysis of p53 in telomere-related aging has been hampered by early tumor formation in p53 knockout mice. Here we analyzed the functional consequences of conditional p53 deletion. Intestinal deletion of p53 shortened the lifespan of telomere-dysfunctional mice without inducing tumor formation. In contrast to p21 deletion, the deletion of p53 impaired the depletion of chromosomal-instable intestinal stem cells in aging telomere-dysfunctional mice. These instable stem cells contributed to epithelial regeneration leading to an accumulation of chromosomal instability, increased apoptosis, altered epithelial cell differentiation and premature intestinal failure. Together, these results provide the first experimental evidence for an organ system in which p53-dependent mechanisms prevent tissue destruction in response to telomere dysfunction by depleting genetically instable stem cells.

Indexed as

Chromosomal InstabilityGene DeletionAgingAnimalsCell CycleDNA DamageGenomeIntestinal MucosaIntestinesMiceMice, KnockoutStem CellsTelomereTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID19718028
OpenAlexW2098337475

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.