Evidence map›Paper›PMID 25719246›Full record

ArticleCell death & disease2015

p53 is active in murine stem cells and alters the transcriptome in a manner that is reminiscent of mutant p53.

H Yan, V Solozobova, P Zhang, O Armant, B Kuehl, G Brenner-Weiss, C Blattner

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Amniotic Fluid Cells, Stem Cells, and p53: Can We Stereotype p53 Functions?International journal of molecular sciences · 2019
    Review
  5. p53 Is Active in Human Amniotic Fluid Stem Cells.Stem cells and development · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. 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

7 authors at 1 institution in 1 country.

H Yan1] Karlsruhe Institute of Technology, Institute of Toxicology and Genetics, Karlsruhe, Germany [2] University of Heidelberg, Heidelberg, Germany.
V SolozobovaKarlsruhe Institute of Technology, Institute of Toxicology and Genetics, Karlsruhe, Germany.
P Zhang1] Karlsruhe Institute of Technology, Institute of Toxicology and Genetics, Karlsruhe, Germany [2] University of Heidelberg, Heidelberg, Germany.
O ArmantKarlsruhe Institute of Technology, Institute of Toxicology and Genetics, Karlsruhe, Germany.
B KuehlKarlsruhe Institute of Technology, Institute of Functional Interfaces, Karlsruhe, Germany.
G Brenner-WeissKarlsruhe Institute of Technology, Institute of Functional Interfaces, Karlsruhe, Germany.
C BlattnerKarlsruhe Institute of Technology, Institute of Toxicology and Genetics, Karlsruhe, Germany.
Karlsruhe Institute of Technology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since it was found that p53 is highly expressed in murine embryonic stem cells, it remained a mystery whether p53 is active in this cell type. We show that a significant part of p53 is localised in the nucleus of murine embryonic stem cells and that the majority of this nuclear p53 is bound to DNA. According to its nuclear localisation, we show that p53 alters the transcriptional program of stem cells. Nevertheless, the anti-proliferative activity of p53 is compromised in stem cells, and this control is due, at least in part, to the high amount of MdmX that is present in embryonic stem cells and bound to p53. Instead of the anti-proliferative activity that p53 has in differentiated cells, p53 controls transcription of pro-proliferative genes in embryonic stem cells including c-myc and c-jun. The impeded anti-proliferative activity of p53 and the induction of certain proto-oncogenes by p53 in murine embryonic stem cells can explain why stem cells proliferate efficiently despite having high levels of p53.

Indexed as

AnimalsCell DifferentiationCell NucleusEmbryonic Stem CellsMiceMutationTranscriptomeTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID25719246
PMCPMC4669809
OpenAlexW1963641234

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.