P450 and human cancer

Jpn J Cancer Res. 1991 Dec;82(12):1325-35. doi: 10.1111/j.1349-7006.1991.tb01800.x.

Abstract

Most of the chemical carcinogens in our environment are activated mainly by a restricted number of cytochrome P450 species, P450 1A1, 1A2, 2E1, and 3A. This metabolic activation of procarcinogens is a crucial part of the initial host response to the environmental exposure, since most chemical carcinogens do not show any carcinogenicity by themselves. Inter-individual variability in the metabolic activity may thus be a key host factor to explain the differences in susceptibility to chemical carcinogenesis among individuals. Recent studies on P450s in cancer etiology have provided some valuable insights into this problem.

Publication types

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

MeSH terms

  • Animals
  • Biotransformation / genetics
  • Carcinogens / pharmacokinetics
  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / metabolism*
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Neoplasms / chemically induced
  • Neoplasms / enzymology*
  • Neoplasms / etiology

Substances

  • Carcinogens
  • Isoenzymes
  • Cytochrome P-450 Enzyme System