p53: its mutations and their impact on transcription

Subcell Biochem. 2014:85:71-90. doi: 10.1007/978-94-017-9211-0_4.

Abstract

p53 is a tumor suppressor protein whose key function is to maintain the integrity of the cell. Mutations in p53 have been found in up to 50 % of all human cancers and cause an increase in oncogenic phenotypes such as proliferation and tumorigenicity. Both wild-type and mutant p53 have been shown to transactivate their target genes, either through directly binding to DNA, or indirectly through protein-protein interactions. This review discusses possible mechanisms behind both wild-type and mutant p53-mediated transactivation and touches on the concept of addiction to mutant p53 of cancer cells and how that may be used for future therapies.

Publication types

  • Review

MeSH terms

  • Animals
  • Genes, p53*
  • Humans
  • Mice
  • Models, Animal
  • Mutation*
  • Neoplasms / genetics
  • Oncogenes
  • Transcription, Genetic / genetics*