Classic and novel roles of p53: prospects for anticancer therapy

Trends Mol Med. 2007 May;13(5):192-9. doi: 10.1016/j.molmed.2007.03.002. Epub 2007 Mar 23.

Abstract

The tumor suppressor p53 is a transcription factor that is frequently inactivated in human tumors. Therefore, restoring its function has been considered an attractive approach to restrain cancer. Typically, p53-dependent growth arrest, senescence and apoptosis of tumor cells have been attributed to transcriptional activity of nuclear p53. Notably, wild-type p53 gain-of-function enhances cancer resistance in the mouse, but it also accelerates aging in some models, possibly due to altered p53 activity. Therefore, the emerging evidence of mitochondrial transcription-independent activities of p53 has raised high expectations. Here, we review new developments in transcription-dependent and transcription-independent p53 functions, recent advances in targeting p53 for cancer treatment and the pitfalls of moving from the laboratory research to the clinical setting.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / genetics
  • Animals
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genome, Human
  • Humans
  • Mice
  • Models, Biological
  • Neoplasms / therapy*
  • Proto-Oncogene Proteins c-bcl-2 / physiology
  • Transcriptional Activation / drug effects
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / physiology*
  • bcl-X Protein / physiology

Substances

  • Antineoplastic Agents
  • BCL2L1 protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • bcl-X Protein