韩国乳腺癌的遗传易感性-分子流行病学方法

D. Kang, D. Noh
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摘要

乳腺癌是西方国家女性中最常见的癌症,其患病率在亚洲也在上升。(1,2) 1994年,经世界人口调整后,韩国女性乳腺癌发病率为10.9 / 10万,远低于西方国家,甚至低于亚洲其他国家。与乳腺癌有关的主要危险因素可以追溯到影响终生激素水平的生殖事件(3,4)。然而,很大一部分乳腺癌病例不能用上述危险因素来解释。如果暴露于特定的环境因素,对个体易患乳腺癌的易感性因素的识别,可能会进一步深入了解这种恶性肿瘤的病因。代谢环境致癌物能力的遗传差异最近被认为改变了个体对乳腺癌的易感性。因此,新的乳腺癌易感基因的鉴定可能会对乳腺肿瘤的发生产生新的见解,并可能为未来的治疗发展提供靶点。在这方面,最有趣的候选基因包括那些介导一系列功能的基因,如致癌物质代谢、DNA修复、类固醇激素代谢、信号转导和细胞周期控制。虽然这些低外显率易感基因对乳腺癌发展的相对风险通常低于高外显率易感基因(如BRCA1、BRCA2等),但低外显率基因的归因风险远高于高外显率基因,因为其变异等位基因在一般人群中的频率更高。因此,这些低外显率基因具有更高的公共卫生意义,通过使用它们,可能对人类乳腺癌的发生机制有更深入的了解,并对具有“高危”基因型的个体有针对性的预防方法(表1)。我们在韩国进行了一项基于医院的病例对照研究,以进一步评估参与致癌物代谢的选定基因的遗传多态性的潜在修饰作用。雌激素代谢、信号转导和DNA修复,同时考虑到这些因素与已知乳腺癌危险因素之间的潜在相互作用(表2)。选定基因的结果将在这篇小型综述中展示。
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Genetic Susceptibility of Breast Cancer in Korea -Molecular Epidemiological Approaches-
Breast cancer is the most prevalent cancer among women in Western countries and its prevalence is also increasing in Asia. (1,2) In 1994, the incidence rate of female breast cancer in Korea, adjusted for the world population, was 10.9 per 100,000, which was far lower than those of Western countries and even lower than those of other Asian countries. The major risk factors relating to breast cancer can be traced to reproductive events influencing lifetime levels of hormones.(3,4) A large proportion of breast cancer cases cannot, however, be explained by the above risk factors. The identification of susceptibility factors predisposing an individual to breast cancer, if exposed to particular environmental agents, could possibly give further insight into the etiology of this malignancy. Inherited differences in the capacity to metabolize environmental carcinogens have recently been suggested to modify individual susceptibilities to breast cancer. Therefore, the identification of new breast cancer susceptibility genes might yield new insight into breast tumorigenesis, and could provide targets for future therapeutic developments. In this respect the most interesting candidate genes include those mediating a range of functions, such as carcinogen metabolism, DNA repair, steroid hormone metabolism, signal transduction, and cell cycle control. Although the relative risks of these low penetrance susceptibility genes, to the development of breast cancer, are generally lower than those from high penetrance susceptibility genes (e.g., BRCA1, BRCA2, etc.), the attributable risk of low penetrance genes are much higher than those of the high penetrance genes, since the frequency of their variant alleles are higher in the general population. Thus, higher public health significance lays with these low penetrance genes, With their use it may be possible to obtain greater mechanistic insights into human breast carcinogenesis as well as targeted preventive approaches to the individuals with ‘at risk’ genotypes (Table 1). We have conducted a hospital based case-control study in South Korea to further evaluate the potential modifying role of the genetic polymorphisms of selected genes involved in the metabolism of carcinogens, estrogen metabolism, signal transduction, and DNA repair, also taking into account the potential interaction between these and known risk factors of breast cancer (Table 2). The results from selected genes will be presented in this mini-review.
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