Evidence map›Paper›PMID 17032926›Full record

ArticleBlood2007

The impact of altered p53 dosage on hematopoietic stem cell dynamics during aging.

Melissa Dumble, Lynette Moore, Stuart M Chambers, Hartmut Geiger, Gary Van Zant, Margaret A Goodell, Lawrence A Donehower

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 239 citations in OpenAlex.

  1. Aging and cancer: current understandings and future perspectives.Signal transduction and targeted therapy · 2026
    Review
  2. DCAF13 Safeguards Hematopoietic Stem Cells via RRS1-Regulated Ribosome Biogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  14. Loss ofHaematologica · 2022
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

70 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

7 authors at 5 institutions in 3 countries.

Melissa DumbleDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, and Division of Experimental Hematology, Cincinnati Children's Hospital Medical Center, OH, USA.
Lynette Moore
Stuart M Chambers
Hartmut Geiger
Gary Van Zant
Margaret A Goodell
Lawrence A Donehower
Institut de Biologie Moléculaire et Cellulaire · FRCincinnati Children's Hospital Medical Center · USInstitute of Molecular and Cell Biology · RUMarkey Cancer Center · USPediatrics and Genetics · US

Funding

Gene Expression and Discovery in Liver and Gut Stem Cel*U01DK063588 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI DARLINGTON, GRETCHEN J. · 2002 to 2004
$4.1M
CELL &MOLECULAR BIOLOGY OF AGINGT32AG000183 · NIA · BAYLOR COLLEGE OF MEDICINE · PI DONEHOWER, LAWRENCE A. · 1989 to 2015
$3.7M
P53 and Organismal AgingR01AG019693 · NIA · BAYLOR COLLEGE OF MEDICINE · PI DONEHOWER, LAWRENCE A. · 2002 to 2006
$2.7M
Genes affecting aging stem cell populationsR01AG020917 · NIA · UNIVERSITY OF KENTUCKY · PI VAN ZANT, GARY · 2002 to 2006
$1.6M
Basic Research In Personality: Age Changes and DifferencesZ01AG000183 · NIA · NATIONAL INSTITUTE ON AGING · PI COSTA, PAUL T · 1990 to 2008
$917k
Intramural NIH HHS Z01 AG000183NIA NIH HHS AG000183NIA NIH HHS AG19693NIA NIH HHS AG20917NIA NIH HHS R01 AG019693NIA NIH HHS R01 AG020917NIA NIH HHS T32 AG000183NIDDK NIH HHS U01 DK063588NIDDK NIH HHS U01 DK63588
6 · The paper itself

Abstract

A temporal decline in tissue stem cell functionality may be a key component of mammalian aging. The tumor suppressor p53 has recently been implicated as a potential regulator of aging. We examined age-associated hematopoietic stem cell (HSC) dynamics in mice with varying p53 activities. Reduced p53 activity in p53+/- mice was associated with higher numbers of proliferating hematopoietic stem and progenitor cells in old age compared with aged wild-type (p53+/+) mice. We also assessed HSC dynamics in a p53 mutant mouse model (p53+/m) with higher apparent p53 activity than wild-type mice. The p53 hypermorphic (p53+/m) mice display phenotypes of premature aging. Many aged p53+/m organs exhibit reduced cellularity and atrophy, suggesting defects in stem-cell regenerative capacity. HSC numbers from old p53+/m mice fail to increase with age, unlike those of their p53+/+ and p53+/- counterparts. Moreover, transplantation of 500 HSCs from old p53+/m mice into lethally irradiated recipients resulted in reduced engraftment compared with old wild-type p53+/+ and p53+/- HSCs. Thus, alteration of p53 activity affects stem-cell numbers, proliferation potential, and hematopoiesis in older organisms, supporting a model in which aging is caused in part by a decline in tissue stem cell regenerative function.

Indexed as

AgingAnimalsCell CountCell ProliferationHematopoiesisHematopoietic Stem CellsMiceMice, KnockoutTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID17032926
PMCPMC1794064
OpenAlexW2148479228

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.