Association between lung cancer and microsomal epoxide hydrolase genotypes

Cancer Res. 1998 Dec 1;58(23):5291-3.

Abstract

Microsomal epoxide hydrolase (mEH) is involved in the metabolism of tobacco-derived carcinogens. Polymorphisms in exons 3 and 4 of the EPHX gene have been reported to be associated with variations in mEH activity. We examined whether the predicted mEH activity modified the lung cancer risk among 150 cases and 172 controls, all French Caucasian smokers. A significant association was found between predicted mEH activity and lung cancer (P < 0.02), with a dose-effect relationship (P < 0.005). The risks associated with intermediate and high activities, compared to low activity, were 1.65 (95% CI, 0.95-2.86) and 2.66 (95% CI, 1.33-5.33), respectively. The effect of mEH activity on lung cancer risk was not significantly modified by smoking exposure, CYP1A1 genotype, or GSTM1 genotype. mEH may thus be an important genetic determinant of smoking-induced lung cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Small Cell / enzymology*
  • Carcinoma, Small Cell / etiology
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Squamous Cell / enzymology*
  • Carcinoma, Squamous Cell / etiology
  • Carcinoma, Squamous Cell / genetics
  • Case-Control Studies
  • Cytochrome P-450 CYP1A1 / genetics
  • Cytochrome P-450 CYP1A1 / metabolism
  • Epoxide Hydrolases / genetics*
  • Exons
  • Female
  • Genotype
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Humans
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / etiology
  • Lung Neoplasms / genetics
  • Male
  • Microsomes / enzymology
  • Middle Aged
  • Polymorphism, Genetic
  • Risk Factors
  • Smoking / adverse effects

Substances

  • Cytochrome P-450 CYP1A1
  • Glutathione Transferase
  • Epoxide Hydrolases