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Volume 34, Issue 2, Pages 178-183 (April 2010)


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CYP2C9 genotype does not affect risk of tobacco-related cancer in the general population

Diljit Kaur-Knudsenab, Børge Grønne Nordestgaardabc, Stig Egil BojesenabcCorresponding Author Informationemail address

Accepted 6 January 2010. published online 21 January 2010.

Abstract 

Background: CYP2C9 enzymes are important in the metabolism of procarcinogenic chemicals such as polycyclic aromatic hydrocarbons (PAHs) found in tobacco smoke. Two functional variants in the CYP2C9 gene (CYP2C9*2 and CYP2C9*3) are known to be associated with decreased enzyme activity towards tolbutamide and warfarin, while this has not been investigated for PAHs. We hypothesised that these two variants in the CYP2C9 gene influence risk of tobacco-related cancer. Methods: In a prospective study of the general population (n=10 392) with 60 years of follow-up, the Copenhagen City Heart Study, we associated two variants of CYP2C9 (CYP2C9*2 and CYP2C9*3) with risk of tobacco-related cancer and all cancer. All results were re-tested in a cross-sectional study of the general population (n=36 856), the Copenhagen General Population Study. Results: We found no association between any of the CYP2C9 genotypes and risk of tobacco-related cancer, individual tobacco-related cancers, or all cancer. For the combined carriers (any CYP2C9*2 or CYP2C9*3 heterozygotes or homozygotes) vs. non-carriers we had 90% statistical power to exclude measures of relative risks below/above 0.8/1.2 and 0.9/1.1 in the Copenhagen City Heart Study and below/above 0.8/1.3 and 0.9/1.1 in the Copenhagen General Population Study for tobacco-related cancer and all cancer, respectively. Conclusion: Genetic variations in CYP2C9 do not affect risk of tobacco-related cancers.

a Department of Clinical Biochemistry and The Copenhagen General Population Study, Herlev Hospital, Copenhagen University Hospital, Herlev Ringvej 75, DK-2730 Herlev, Denmark

b Department of Diagnostic Sciences, Faculty of Health Sciences, University of Copenhagen, Denmark

c The Copenhagen City Heart Study, Bispebjerg Hospital, Copenhagen University Hospital, Denmark

Corresponding Author InformationCorresponding author at: Department of Clinical Biochemistry, 54M1, Herlev Hospital, Copenhagen University Hospital, Herlev Ringvej 75, DK-2730 Herlev, Denmark. Tel.: +45 4488 3843; fax: +45 4488 3311.

PII: S1877-7821(10)00006-8

doi:10.1016/j.canep.2010.01.003


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