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Cancer Epidemiology Biomarkers & Prevention Vol. 11, 895-900, September 2002
© 2002 American Association for Cancer Research

Multiple Cancers Associated with Esophageal and Oropharyngolaryngeal Squamous Cell Carcinoma and the Aldehyde Dehydrogenase-2 Genotype in Male Japanese Drinkers1

Akira Yokoyama2, Hiroshi Watanabe, Haruhiko Fukuda, Tatsumasa Haneda, Hoichi Kato, Tetsuji Yokoyama, Taro Muramatsu, Hiroyasu Igaki and Yuji Tachimori

National Institute on Alcoholism, Kurihama National Hospital, Yokosuka, Kanagawa 239-0841 [A. Y.]; Departments of Surgery [H. W.] and Neuropsychiatry [T. M.], School of Medicine, Keio University, Shinjuku-ku, Tokyo 160-8582; Cancer Information and Epidemiology Division, National Cancer Center Research Institute [H. F.] and Surgery Division, National Cancer Center Hospital [H. K., H. I., Y. T.], Chuo-ku, Tokyo 104-0045; Kamio Memorial Hospital, Chiyoda-ku, Tokyo 101-0063 [T. H.]; and Department of Technology Assessment and Biostatistics, National Institute of Public Health, Wako, Saitama 351-0104 [T. Y.], Japan

Aldehyde dehydrogenase-2 (ALDH2) is a key enzyme for the elimination of acetaldehyde, an established animal carcinogen generated by alcohol metabolism. In the presence of ALDH2*2, a mutant allele that is prevalent in East Asians, this enzyme is inactive, leading to excessive accumulation of acetaldehyde. Only among Japanese alcoholic patients has the positive association between this inactive form of ALDH2 and multiple-field cancerization in the upper aerodigestive tract been demonstrated. Whether this finding could be extended to multiple-cancer patients in general is of great interest, because the prevalence of esophageal cancer with other organ cancers has increased dramatically during recent decades in Japan. This study compared the ALDH2 genotypes of groups of male Japanese drinkers who had either esophageal squamous cell carcinomas (SCCs) with (n = 26) or without (n = 48) multiplicity or oropharyngolaryngeal SCCs with (n = 17) or without (n = 29) multiplicity. After adjustments for age and drinking and smoking habits, logistic regression analysis showed significantly increased risk for each multiplicity associated with either esophageal or oropharyngolaryngeal SCCs in the presence of the ALDH2*2 allele (odds ratio, 5.26; 95% confidence interval, 1.08–51.06 and odds ratio, 7.36; 95% confidence interval, 1.29–80.70, respectively). This study is the first to strongly link inactive ALDH2 with the multiple cancer susceptibility of male Japanese drinkers with either esophageal or oropharyngolaryngeal cancers. A simple questionnaire about both current and past facial flushing after drinking a glass of beer was highly sensitive (95.6%) in detecting inactive ALDH2 in these patients and may be useful for identifying high-risk patients.




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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
Copyright © 2002 by the American Association for Cancer Research.