Shin Aesun, Kim Jeongseon
Cancer Epidemiology Branch, Research Institute, National Cancer Center, Korea.
Asian Pac J Cancer Prev. 2010;11(2):281-7.
Colorectal cancer incidences differ considerably between Western and non-Western countries. In recent years, a dramatic increase in colorectal cancer incidence has been reported in several Asian countries. Immigration studies have suggested that environmental rather than genetic factors are primarily responsible for the international variability and secular trends of colorectal cancer incidence rates. Therefore, not only the main effect of a gene but also the influence of gene-environment interactions on cancer risk are important from the public health perspective. This review encompasses the literature on gene-diet interactions, particularly focusing on meat intake and its association with the risk of colorectal carcinoma or adenomas. It is generally accepted that genotypes which are associated with the higher enzyme activity for metabolic activation or lower activity for detoxification would affect individual's susceptibility to meat carcinogens. The most intensively studied genes were those involved in xenobiotic metabolism, including N-acetyltransferase (NAT), cytochrome P450 (CYP) families, glutathione S-transferase (GST), and sulfotransferase (SULT). However, the associations were not consistent across studies. The role of genetic polymorphisms and their role in effect modification of environmental carcinogens should be assessed in well-designed large-scale epidemiological studies with comprehensive information for risk factors for better understanding the etiologic role of dietary factors and in developing a personalized cancer prevention strategy in the genome-wide association study era.
西方国家和非西方国家的结直肠癌发病率差异很大。近年来,一些亚洲国家报告了结直肠癌发病率急剧上升。移民研究表明,环境因素而非遗传因素是导致结直肠癌发病率国际差异和长期趋势的主要原因。因此,从公共卫生角度来看,不仅基因的主要作用,而且基因-环境相互作用对癌症风险的影响都很重要。本综述涵盖了关于基因-饮食相互作用的文献,特别关注肉类摄入及其与结直肠癌或腺瘤风险的关联。一般认为,与代谢激活酶活性较高或解毒酶活性较低相关的基因型会影响个体对肉类致癌物的易感性。研究最深入的基因是那些参与异源物质代谢的基因,包括N-乙酰转移酶(NAT)、细胞色素P450(CYP)家族、谷胱甘肽S-转移酶(GST)和磺基转移酶(SULT)。然而,各研究之间的关联并不一致。在设计良好的大规模流行病学研究中,应评估基因多态性的作用及其在环境致癌物效应修饰中的作用,并提供全面的风险因素信息,以便更好地理解饮食因素的病因学作用,并在全基因组关联研究时代制定个性化的癌症预防策略。