Ultraviolet radiation-induced p53 responses in the epidermis are differentiation-dependent

J Cutan Med Surg. 1999 Jul;3(5):280-3. doi: 10.1177/120347549900300511.

Abstract

Background: The tumour suppressor, p53, is recognized as a crucial molecule in regulating cellular responses to various DNA-damaging agents. Very early on in the development of nonmelanoma cancers p53 is mutated or lost, suggesting that p53 is crucial in protecting normal keratinocytes from the harmful effects of ultraviolet (UV) radiation.

Objective: Using two mouse models, one with multiple copies of mutant p53 and the other a p53 "knockout," our laboratory has examined a role for p53 in UV-induced DNA damage and determined if these effects are differentiation dependent.

Conclusion: We outline in this review a proposed model reflecting differentiation-dependent p53 regulation of UV-induced responses in keratinocytes. After exposure to UV, basal keratinocytes repair damaged DNA, whereas differentiating keratinocytes undergo cell death, both processes are regulated by p53.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis
  • Cell Cycle
  • DNA / radiation effects*
  • DNA Repair
  • Epidermis / pathology
  • Epidermis / radiation effects*
  • Genes, p53*
  • Humans
  • Keratinocytes / radiation effects*
  • Mice
  • Tumor Suppressor Protein p53 / physiology
  • Tumor Suppressor Protein p53 / radiation effects*
  • Ultraviolet Rays*

Substances

  • Tumor Suppressor Protein p53
  • DNA