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Carcinogenesis, Vol. 20, No. 9, 1877-1881, September 1999
© 1999 Oxford University Press


Short Communications

NAT2 slow acetylator genotype is associated with increased risk of lung cancer among non-smoking Chinese women in Singapore

Adeline Seow7, Bin Zhao1, Wee-Teng Poh4, Ming Teh2, Philip Eng5, Yee-Tang Wang6, Wan-Cheng Tan3, Edmund J.D. Lee1 and Hin-Peng Lee

Department of Community, Occupational and Family Medicine, Faculty of Medicine, National University of Singapore, 16 Medical Drive, Singapore, 117597,
1 Department of Pharmacology,
2 Department of Pathology and
3 Department of Medicine, Faculty of Medicine, National University of Singapore, Lower Kent Ridge Road, Singapore, 119260,
4 Department of Pathology and
5 Department of Respiratory and Critical Care Medicine, Singapore General Hospital, Outram Road, Singapore, 169608 and
6 Department of Respiratory Medicine, Tan Tock Seng Hospital, Moulmeri Road, Singapore 308433

Among non-smokers, the factors resulting in lung carcinogenesis are poorly understood. We conducted a hospital-based case-control analysis of 294 Chinese women, of whom 217 were non-smokers, to evaluate the role of polymorphic N-acetyltransferase (NAT2) as a susceptibility factor for the disease. The proportion of slow acetylator genotypes among non-smoking cases (n = 92) and controls (n = 125) was 38.0 and 24.0%, respectively [odds ratio (OR) 2.0, 95% confidence interval (CI) 1.1–3.7]. No effect of NAT2 genotype was seen among smokers. Among non-smokers, the effect was marked for adenocarcinomas (OR 2.1, 95% CI 1.1–4.0). As NAT2 activity is known to modify risk of arylamine-induced carcinogenesis, our results suggest that exposure to arylamines in the environment may play a role in risk of lung cancer among non-smokers.

Abbreviations: 4-ABP, 4-aminobiphenyl; NAT2, N-acetyltransferase-2.

7 To whom correspondence should be addressed Email: cofseowa{at}nus.edu.sg


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