Evidence map›Paper›PMID 19755852›Full record

ReviewCell cycle (Georgetown, Tex.)2009

The p53 tumor suppressor protein is a critical regulator of hematopoietic stem cell behavior.

Yan Liu, Shannon E Elf, Takashi Asai, Yasuhiko Miyata, Yuhui Liu, Goro Sashida, Gang Huang, Silvana Di Giandomenico, Andrew Koff, Stephen D Nimer

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 65 citations in OpenAlex.

  1. Unraveling the role ofHemaSphere · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. An In Vitro Model of Cellular Quiescence in Primary Human Dermal Fibroblasts.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. DNA Damage Response in Hematopoietic Stem Cell Ageing.Genomics, proteomics & bioinformatics · 2016
    Review
  16. Dual effect of oxidative stress on leukemia cancer induction and treatment.Journal of experimental & clinical cancer research : CR · 2014
    Review
  17. Article
  18. Article
  19. Article
  20. Therapeutic targeting of the p53 pathway in cancer stem cells.Expert opinion on therapeutic targets · 2012
    Review
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

10 authors at 2 institutions in 1 country.

Yan LiuMolecular Pharmacology and Chemistry Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Shannon E Elf
Takashi Asai
Yasuhiko Miyata
Yuhui Liu
Goro Sashida
Gang Huang
Silvana Di Giandomenico
Andrew Koff
Stephen D Nimer
New York Proton Center · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
FUNCTION OF MEF IN HEMATOPOIETIC CELLSR01DK052208 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI NIMER, STEPHEN D. · 1997 to 2011
$3.1M
Function of MEF in Hematopoietic CellsR56DK052208 · NIDDK · SLOAN-KETTERING INST CAN RESEARCH · PI NIMER, STEPHEN DAVID · 2007 to 2007
$500k
NCI NIH HHS P30 CA008748NIDDK NIH HHS R01 DK052208NIDDK NIH HHS R01 DK52208NIDDK NIH HHS R56 DK052208
6 · The paper itself

Abstract

In response to diverse stresses, the tumor suppressor p53 differentially regulates its target genes, variably inducing cell-cycle arrest, apoptosis or senescence. Emerging evidence indicates that p53 plays an important role in regulating hematopoietic stem cell (HSC) quiescence, self-renewal, apoptosis and aging. The p53 pathway is activated by DNA damage, defects in ribosome biogenesis, oxidative stress and oncogene induced p19 ARF upregulation. We present an overview of the current state of knowledge about p53 (and its target genes) in regulating HSC behavior, with the hope that understanding the molecular mechanisms that control p53 activity in HSCs and how p53 mutations affect its role in these events may facilitate the development of therapeutic strategies for eliminating leukemia (and cancer) propagating cells.

Indexed as

ApoptosisCell CycleCellular SenescenceDNA DamageHematopoietic Stem CellsProto-Oncogene Proteins c-mdm2Transcription FactorsTumor Suppressor Protein p53Proto-Oncogene Proteins c-mdm2Transcription FactorsTumor Suppressor Protein p53

Identifiers

PMID19755852
PMCPMC4637974
OpenAlexW1977376434

What OpenQuestion holds

Textmetadata
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.