Limiting the power of p53 through the ubiquitin proteasome pathway

Genes Dev. 2014 Aug 15;28(16):1739-51. doi: 10.1101/gad.247452.114.

Abstract

The ubiquitin proteasome pathway is critical in restraining the activities of the p53 tumor suppressor. Numerous E3 and E4 ligases regulate p53 levels. Additionally, deubquitinating enzymes that modify p53 directly or indirectly also impact p53 function. When alterations of these proteins result in increased p53 activity, cells arrest in the cell cycle, senesce, or apoptose. On the other hand, alterations that result in decreased p53 levels yield tumor-prone phenotypes. This review focuses on the physiological relevance of these important regulators of p53 and their therapeutic implications.

Keywords: Mdm2; mouse models; p53 regulation; ubiquitination.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Humans
  • Proteasome Endopeptidase Complex / metabolism*
  • Protein Stability
  • Proto-Oncogene Proteins c-mdm2 / metabolism
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Ubiquitin / metabolism*
  • Ubiquitination

Substances

  • Tumor Suppressor Protein p53
  • Ubiquitin
  • Proto-Oncogene Proteins c-mdm2
  • Proteasome Endopeptidase Complex