Evidence map›Paper›PMID 22624716›Full record

ArticleCancer cell2012

ATM phosphorylation of Mdm2 Ser394 regulates the amplitude and duration of the DNA damage response in mice.

Hugh S Gannon, Bruce A Woda, Stephen N Jones

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
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  7. International cancer conference journal · 2023
    Article
  8. Review
  9. Article
  10. Mdm2 phosphorylation by Akt regulates the p53 response to oxidative stress to promote cell proliferation and tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Understanding p53 functions through p53 antibodies.Journal of molecular cell biology · 2019
    Review
  18. Article
  19. Considering the Role of Murine Double Minute 2 in the Cardiovascular System?Frontiers in cell and developmental biology · 2019
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Hugh S GannonDepartment of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Bruce A WodaDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Stephen N JonesDepartment of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA; Department of Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA. Electronic address: stephen.jones@umassmed.edu.
University of Massachusetts Chan Medical School · US

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
The Role of MDM Proteins in Cell Growth and TumorigenesisR01CA077735 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JONES, STEPHEN, ZHANG, HONG · 1999 to 2019
$5.7M
The Role of MDM Proteins in Cell Growth and TumorigenesisR56CA077735 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JONES, STEPHEN · 2009 to 2009
$324k
NCI NIH HHS CA077735NCI NIH HHS R01 CA077735NCI NIH HHS R56 CA077735NIDDK NIH HHS DK32520NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

DNA damage induced by ionizing radiation activates the ATM kinase, which subsequently stabilizes and activates the p53 tumor suppressor protein. Although phosphorylation of p53 by ATM was found previously to modulate p53 levels and transcriptional activities in vivo, it does not appear to be a major regulator of p53 stability. We have utilized mice bearing altered Mdm2 alleles to demonstrate that ATM phosphorylation of Mdm2 serine 394 is required for robust p53 stabilization and activation after DNA damage. In addition, we demonstrate that dephosphorylation of Mdm2 Ser394 regulates attenuation of the p53-mediated response to DNA damage. Therefore, the phosphorylation status of Mdm2 Ser394 governs p53 protein levels and functions in cells undergoing DNA damage.

Indexed as

DNA DamageAnimalsApoptosisAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsDNA-Binding ProteinsEnzyme ActivationIntestine, SmallMiceMice, 129 StrainMice, Inbred C57BLMutation, MissensePhosphorylationProtein Serine-Threonine KinasesProtein StabilityProto-Oncogene Proteins c-mdm2Ataxia Telangiectasia Mutated ProteinsAtm protein, mouseCell Cycle ProteinsDNA-Binding ProteinsMdm2 protein, mouseProtein Serine-Threonine KinasesProto-Oncogene Proteins c-mdm2SerineTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID22624716
PMCPMC3360886
OpenAlexW2117932700

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.