| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Laboratory of Drug Metabolism, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812 [N. A., M. M., Y. U., T. K.]; Department of Internal Medicine and Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045 [H. K.]; First Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo 060-0815 [H. D-A.]; Maruyama Clinic, Sapporo 064-0820 [Y. S.]; Biology Division, National Cancer Center Research Institute, Tokyo 104-0045 [J. Y.]; Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Toyama 930-0152 [N. N.]; and Department of Internal Medicine, Gunma University School of Medicine, Gunma 371-0034 [K. S.], Japan
Cytochrome P450 2A6 (CYP2A6) is the principal enzyme involved in the metabolic activation of tobacco-specific nitrosamines to their ultimate carcinogenic forms and metabolism of nicotine. We investigated the effects of the CYP2A6*4, an entire CYP2A6 gene deletion-type polymorphism, on lung cancer risk and daily cigarette consumption in Japanese male smokers via a hospital-based case control study. The frequency of the CYP2A6*4 variant was compared in 370 lung cancer patients and 380 control smokers. A markedly reduced adjusted odds ratio for lung cancer risk, 0.23 [95% confidence interval, 0.080.67], was seen in the group with homozygous deletion (*4/*4) when the odds ratio for a group with homozygous wild (*1A/*1A) was defined to be 1.00 by logistic regression. The subjects with lung cancer were additionally divided into three groups according to the histological classification of the cancer and examined for an association with the CYP2A6 polymorphism. The *4/*4 genotype was not found in patients with squamous cell carcinoma (0 of 105) or small cell carcinoma (0 of 44), indicating that subjects with the *4/*4 genotype have low risk for lung cancers, particularly those caused by tobacco smoke. Furthermore, a significant reduction of daily cigarette consumption was observed in smokers with the *4/*4 genotype, suggesting a possibility that complete lack of CYP2A6 appeared to affect the smoking behavior. These data suggest that male smokers possessing the *1A/*1A genotype have higher risk for tobacco-induced lung cancers.
This article has been cited by other articles:
![]() |
A. S. Lee, M. Gutierrez-Arcelus, G. H. Perry, E. J. Vallender, W. E. Johnson, G. M. Miller, J. O. Korbel, and C. Lee Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies Hum. Mol. Genet., April 15, 2008; 17(8): 1127 - 1136. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. H. Yoo, M. W. Lee, Y. C. Kim, C.-H. Yun, and D.-H. Kim Mechanism-Based Inactivation of Cytochrome P450 2A6 by Decursinol Angelate Isolated from Angelica Gigas Drug Metab. Dispos., October 1, 2007; 35(10): 1759 - 1765. [Abstract] [Full Text] [PDF] |
||||
![]() |
Amal Al Omari and D. J. Murry Pharmacogenetics of the Cytochrome P450 Enzyme System: Review of Current Knowledge and Clinical Significance Journal of Pharmacy Practice, June 1, 2007; 20(3): 206 - 218. [Abstract] [PDF] |
||||
![]() |
V. Malaiyandi, S. D. Goodz, E. M. Sellers, and R. F. Tyndale CYP2A6 Genotype, Phenotype, and the Use of Nicotine Metabolites as Biomarkers during Ad libitum Smoking. Cancer Epidemiol. Biomarkers Prev., October 1, 2006; 15(10): 1812 - 1819. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Casella, M. Miniati, S. Monti, F. Minichilli, F. Bianchi, and S. Simi No evidence of chromosome damage in chronic obstructive pulmonary disease (COPD) Mutagenesis, March 1, 2006; 21(2): 167 - 171. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Kim, Z.-L. Wu, and F. P. Guengerich Analysis of Coumarin 7-Hydroxylation Activity of Cytochrome P450 2A6 using Random Mutagenesis J. Biol. Chem., December 2, 2005; 280(48): 40319 - 40327. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Miyazaki, H. Yamazaki, H. Takeuchi, K. Saoo, M. Yokohira, K.-i. Masumura, T. Nohmi, Y. Funae, K. Imaida, and T. Kamataki Mechanisms of chemopreventive effects of 8-methoxypsoralen against 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced mouse lung adenomas Carcinogenesis, November 1, 2005; 26(11): 1947 - 1955. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-H. Yun, K.-H. Kim, M. W. Calcutt, and F. P. Guengerich Kinetic Analysis of Oxidation of Coumarins by Human Cytochrome P450 2A6 J. Biol. Chem., April 1, 2005; 280(13): 12279 - 12291. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Hukkanen, P. Jacob III, and N. L. Benowitz Metabolism and Disposition Kinetics of Nicotine Pharmacol. Rev., March 1, 2005; 57(1): 79 - 115. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. R. Spitz, X. Wu, and G. Mills Integrative Epidemiology: From Risk Assessment to Outcome Prediction J. Clin. Oncol., January 10, 2005; 23(2): 267 - 275. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Fujieda, H. Yamazaki, T. Saito, K. Kiyotani, M. A. Gyamfi, M. Sakurai, H. Dosaka-Akita, Y. Sawamura, J. Yokota, H. Kunitoh, et al. Evaluation of CYP2A6 genetic polymorphisms as determinants of smoking behavior and tobacco-related lung cancer risk in male Japanese smokers Carcinogenesis, December 1, 2004; 25(12): 2451 - 2458. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Matsumura, T. Saito, Y. Takahashi, T. Ozeki, K. Kiyotani, M. Fujieda, H. Yamazaki, H. Kunitoh, and T. Kamataki Identification of a Novel Polymorphic Enhancer of the Human CYP3A4 Gene Mol. Pharmacol., February 1, 2004; 65(2): 326 - 334. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Takeuchi, K. Saoo, M. Yokohira, M. Ikeda, H. Maeta, M. Miyazaki, H. Yamazaki, T. Kamataki, and K. Imaida Pretreatment with 8-Methoxypsoralen, a Potent Human CYP2A6 Inhibitor, Strongly Inhibits Lung Tumorigenesis Induced by 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone in Female A/J Mice Cancer Res., November 15, 2003; 63(22): 7581 - 7583. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Wang, W. Tan, B. Hao, X. Miao, G. Zhou, F. He, and D. Lin Substantial Reduction in Risk of Lung Adenocarcinoma Associated with Genetic Polymorphism in CYP2A13, the Most Active Cytochrome P450 for the Metabolic Activation of Tobacco-Specific Carcinogen NNK Cancer Res., November 15, 2003; 63(22): 8057 - 8061. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Zhang, Y. Chen, Y. Liu, X. Ren, Q.-Y. Zhang, M. Caggana, and X. Ding SINGLE NUCLEOTIDE POLYMORPHISMS OF THE HUMAN CYP2A13 GENE: EVIDENCE FOR A NULL ALLELE Drug Metab. Dispos., September 1, 2003; 31(9): 1081 - 1085. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. P. Guengerich Cytochromes P450, Drugs, and Diseases Mol. Interv., June 1, 2003; 3(4): 194 - 204. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Cell Growth & Differentiation |