HIPK2 neutralizes MDM2 inhibition rescuing p53 transcriptional activity and apoptotic function

Valeria Di Stefano, Giovanni Blandino, Ada Sacchi, Silvia Soddu, Gabriella D'Orazi

Research output: Contribution to journalArticle

Abstract

The p53 oncosuppressor protein is subject to negative regulation by MDM2, which efficiently inhibits its activity through an autoregulatory loop. In response to stress, however, p53 undergoes post-translational modifications that allow the protein to escape MDM2 control, accumulate, and become active. Recent studies have shown that, following DNA damage, the HIPK2 serine/threonine kinase binds and phosphorylates p53, inducing p53 transcriptional activity and apoptotic function. Here, we investigated the role of HIPK2 in the activation of p53 in the presence of MDM2. We found that HIPK2 rescues p53 transcriptional activity overcoming MDM2 inhibition, and that restoration of this p53 function induces apoptosis. Recovery of p53-dependent apoptosis is achieved by preventing p53 nuclear export and ubiquitination mediated by MDM2 in vitro and in vivo following genotoxic stress. These results shed new light on the mechanisms by which the HIPK2/p53 pathway promotes apoptosis and suppression of tumorigenesis.

Original languageEnglish
Pages (from-to)5185-5192
Number of pages8
JournalOncogene
Volume23
Issue number30
DOIs
Publication statusPublished - Jul 1 2004

Fingerprint

Apoptosis
DNA Damage
Cell Nucleus Active Transport
Protein-Serine-Threonine Kinases
Ubiquitination
Post Translational Protein Processing
Carcinogenesis
Proteins
In Vitro Techniques

Keywords

  • Apoptosis
  • HIPK2
  • MDM2
  • Nuclear export
  • p53
  • Ubiquitination

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research
  • Genetics

Cite this

HIPK2 neutralizes MDM2 inhibition rescuing p53 transcriptional activity and apoptotic function. / Di Stefano, Valeria; Blandino, Giovanni; Sacchi, Ada; Soddu, Silvia; D'Orazi, Gabriella.

In: Oncogene, Vol. 23, No. 30, 01.07.2004, p. 5185-5192.

Research output: Contribution to journalArticle

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