Meat, metabolic genotypes and risk for colorectal cancer

被引:27
作者
Roberts-Thomson, IC
Butler, WJ
Ryan, P
机构
[1] Queen Elizabeth Hosp, Dept Gastroenterol, Woodville S, SA 5011, Australia
[2] Univ Adelaide, Dept Publ Hlth, Adelaide, SA, Australia
关键词
acetylation; colorectal cancer; meat; metabolic genotypes;
D O I
10.1097/00008469-199906000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Persuasive data exist as to the importance of environmental factors in the pathogenesis of sporadic colorectal cancer. One possibility is that the effect of environmental factors varies between individuals, perhaps on the basis of inherited variation (polymorphism) in genes which influence the activation or inactivation of dietary carcinogens, Thus far, the focus has been on acetylator genes (NAT1, NAT2) and the activation of heterocyclic amines, carcinogens generated by cooking meat for prolonged periods at high temperature. Three case-control studies and one prospective study have shown a consistent trend towards higher risks for cancer with higher intakes of meat in rapid acetylators for NAT1, NAT2 or both genotypes. Other links between meat, cooking methods, metabolic genotypes and risk for cancer might include enhanced activation of polycyclic aromatic hydrocarbons and N-nitroso compounds by variant genotypes of CYP1A1 and CYP2E1, respectively, and modulation by meat of the protective effect of the epsilon 4 allele of apolipoprotein E on risk for cancer of the proximal colon, (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:207 / 211
页数:5
相关论文
共 19 条
[1]   Cigarette smoking, N-acetyltransferase 2 genetic polymorphisms, and breast cancer risk [J].
Ambrosone, CB ;
Freudenheim, JL ;
Graham, S ;
Marshall, JR ;
Vena, JE ;
Brasure, JR ;
Michalek, AM ;
Laughlin, R ;
Nemoto, T ;
Gillenwater, KA ;
Harrington, AM ;
Shields, PG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (18) :1494-1501
[2]  
Butler WJ, 1997, GASTROENTEROLOGY, V112, pA542
[3]  
Chen J, 1998, CANCER RES, V58, P3307
[4]   Glutathione S-transferase GSTT1 genotypes and susceptibility to cancer: Studies of interactions with GSTM1 in lung, oral, gastric and colorectal cancers [J].
Deakin, M ;
Elder, J ;
Hendrickse, C ;
Peckham, D ;
Baldwin, D ;
Pantin, C ;
Wild, N ;
Leopard, P ;
Bell, DA ;
Jones, P ;
Duncan, H ;
Brannigan, K ;
Alldersea, J ;
Fryer, AA ;
Strange, RC .
CARCINOGENESIS, 1996, 17 (04) :881-884
[5]   METABOLIC PHENOTYPES AND COLORECTAL NEOPLASIA [J].
FETTMAN, MJ ;
BUTLER, RN ;
MCMICHAEL, AJ ;
ROBERTSTHOMSON, IC .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1991, 6 (01) :81-89
[6]   Genes and environment in the etiology of colorectal cancer [J].
Gertig, DM ;
Hunter, DJ .
SEMINARS IN CANCER BIOLOGY, 1998, 8 (04) :285-298
[7]  
HART WJ, 1996, J GASTROEN HEPATOL, V11, pA109
[8]   THE CYP1A1 GENE AND CANCER SUSCEPTIBILITY [J].
KAWAJIRI, K ;
NAKACHI, K ;
IMAI, K ;
WATANABE, J ;
HAYASHI, S .
CRITICAL REVIEWS IN ONCOLOGY/HEMATOLOGY, 1993, 14 (01) :77-87
[9]   Is the development of adenoma and carcinoma in proximal colon related to apolipoprotein E phenotype? [J].
Kervinen, K ;
Sodervik, H ;
Makela, J ;
Lehtola, J ;
Niemi, M ;
Kairaluoma, MI ;
Kesaniemi, YA .
GASTROENTEROLOGY, 1996, 110 (06) :1785-1790
[10]  
LANG NP, 1994, CANCER EPIDEM BIOMAR, V3, P675