Polymorphisms of CYP2A6 and its practical consequences

Br J Clin Pharmacol. 2001 Oct;52(4):357-63. doi: 10.1046/j.0306-5251.2001.01500.x.


CYP2A6 is an hepatic enzyme predominantly with some expression in specialized extrahepatic cell types. The CYP2A6 enzyme has a somewhat restricted active site, accepting only a few xenobiotics as substrates. Interest in CYP2A6 has risen considerably after nicotine and some tobacco specific nitrosamines were established as high-affinity substrates for this enzyme. Recently, the organization and structures of the CYP2A gene cluster and several polymorphic alleles of the CYP2A6 gene have been characterized. Two alleles with a point mutation and at least three different types of gene deletion, all leading to deficient gene function, have been found. The frequencies of these alleles vary considerably among different ethnic populations, the deletion alleles being most common in Orientals (up to 20%). The frequency of point mutations are low in all populations studied thus far (< 3%). Several case-control studies have addressed the relationship between CYP2A6 status and smoking habits as well as the role of CYP2A6 polymorphism in lung cancer risk. Studies in Japanese suggest that CYP2A6 poor metabolizer genotypes result in altered nicotine kinetics and may lower cigarette smoking elicited lung cancer risk, whereas similar studies in Caucasian populations have not revealed any clear associations between variant CYP2A6 genotypes and smoking behaviour or lung cancer predisposition.

Publication types

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

MeSH terms

  • Alleles
  • Aryl Hydrocarbon Hydroxylases*
  • Cotinine / metabolism
  • Cytochrome P-450 CYP2A6
  • Cytochrome P-450 Enzyme System* / genetics
  • Cytochrome P-450 Enzyme System* / metabolism
  • Cytochrome P-450 Enzyme System* / physiology
  • Genetics, Population
  • Genotype
  • Humans
  • Lung Neoplasms / etiology
  • Mixed Function Oxygenases* / genetics
  • Mixed Function Oxygenases* / metabolism
  • Mixed Function Oxygenases* / physiology
  • Nicotine / metabolism
  • Point Mutation / genetics*
  • Polymorphism, Genetic
  • Smoking / adverse effects


  • Nicotine
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Aryl Hydrocarbon Hydroxylases
  • CYP2A6 protein, human
  • Cytochrome P-450 CYP2A6
  • Cotinine