Genetic susceptibility to cancer from exogenous and endogenous exposures

J Cell Biochem Suppl. 1996;25:15-22. doi: 10.1002/(sici)1097-4644(1996)25+<15::aid-jcb2>3.0.co;2-5.

Abstract

The past four decades of epidemiological research have yielded valuable information on the risks of populations to environmental exposures such as tobacco, asbestos, and dietary components. Prevention efforts have been focused on large-scale population-based interventions to minimize exposure to such external carcinogens. While some cancers are beginning to show a decline from changing environmental exposures, hormone-related cancers, such as breast and prostate, are becoming more prevalent. The development of these cancers appears to be closely related to endogenous exposures to circulating steroid hormones. Although prevention trials using antihormone agents are proving successful in some instances, the long-term control of these cancers necessitates a clearer understanding of the metabolism and transport of the relevant hormone in vivo. The revolution in molecular biology has provided powerful genetic tools for evaluating mechanisms of cancer causation as well as the potential to better define individual susceptibility. Using tobacco exposure as an example, we and others have demonstrated that polymorphisms in genes controlling aromatic amine metabolism provide at least a partial explanation for ethnic and individual susceptibility to bladder cancer. Similar studies have examined genetic polymorphisms in the metabolism of tobacco smoke and lung cancer risk, red meat and colorectal cancer, and aflatoxin and liver cancer. Our current studies have pursued a similar paradigm of genetic polymorphism and individual cancer susceptibility in prostate and breast carcinogenesis. We are evaluating polymorphisms in the steroid 5 alpha-reductase type II and androgen receptor genes in relation to prostate cancer based on the evidence that intracellular dihydrotestosterone is the critical "carcinogen." We are pursuing genetic polymorphisms affecting estradiol metabolism, including those in the 17 beta-hydroxysteroid dehydrogenase 2 and estrogen receptor genes as they relate to susceptibility to breast cancer. The potential role of a polymorphism in the cytochrome P450c 17 alpha gene in both breast and prostate cancers is also being examined.

Publication types

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

MeSH terms

  • Adult
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / genetics*
  • Carcinogenicity Tests
  • Cholestenone 5 alpha-Reductase
  • Cytochrome P-450 Enzyme System / genetics
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Hydroxysteroid Dehydrogenases / genetics
  • Male
  • Oxidoreductases / genetics
  • Prostatic Neoplasms / enzymology
  • Prostatic Neoplasms / genetics*
  • Receptors, Androgen / genetics
  • Steroid 17-alpha-Hydroxylase / genetics
  • Urinary Bladder Neoplasms / enzymology
  • Urinary Bladder Neoplasms / genetics*

Substances

  • Receptors, Androgen
  • Cytochrome P-450 Enzyme System
  • Oxidoreductases
  • Hydroxysteroid Dehydrogenases
  • 3(17)-hydroxysteroid dehydrogenase
  • Steroid 17-alpha-Hydroxylase
  • Cholestenone 5 alpha-Reductase