Racial and ethnic factors in the genetic pathogenesis of colorectal cancer.

J M Carethers
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Abstract

Colorectal cancer can develop by two distinct pathogenic mechanisms: one involving chromosomal breakage and aneuploidy (called chromosomal instability) and one involving mutations at DNA micro-satellite sequences (termed micro-satellite instability). Relatively few reports consider these mechanisms of colorectal cancer development across racial or ethnic groups. Available data indicate a moderate increase in colorectal cancer risk among Ashkenazi Jews who have a mutational polymorphism at codon 1307 in the APC gene. In American blacks, there is evidence for a higher prevalence of right-sided colonic tumors and an earlier age of onset of colorectal cancer. In addition, blacks have the highest colon cancer incidence in the United States among ethnic groups and have poorer 5-year survival rates compared with whites. While some differences may be attributed to health care access and socioeconomic differences, these do not completely explain all the variances. In the chromosomal instability pathway, there are polymorphisms within the P53 gene that are more prevalent in blacks, but the significance of these polymorphisms is not fully known. Blacks are more likely to demonstrate micro-satellite instability in their tumors; however, the mechanism for this phenomenon in blacks is unexplored. Differences in diet among racial and ethnic groups and polymorphic variations in drug metabolizing or acetylation genes have not been adequately cataloged. Identification of genetic and environmental factors among racial and ethnic groups should offer some insights into the observed epidemiologic data and advance opportunities to better understand the control and development of colorectal cancer.

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结直肠癌遗传发病的种族和民族因素。
结直肠癌可以通过两种不同的致病机制发展:一种涉及染色体断裂和非整倍体(称为染色体不稳定性),另一种涉及DNA微卫星序列突变(称为微卫星不稳定性)。相对较少的报道考虑到这些机制的结直肠癌的发展跨越种族或民族群体。现有数据表明,在APC基因密码子1307突变多态性的德系犹太人中,结直肠癌的风险适度增加。在美国黑人中,有证据表明右侧结肠肿瘤的患病率更高,结直肠癌的发病年龄也更早。此外,黑人是美国少数民族中结肠癌发病率最高的,与白人相比,黑人的5年生存率较低。虽然一些差异可能归因于医疗保健获取和社会经济差异,但这些差异并不能完全解释所有差异。在染色体不稳定通路中,P53基因内的多态性在黑人中更为普遍,但这些多态性的意义尚不完全清楚。黑人更有可能在肿瘤中表现出微卫星不稳定性;然而,黑人中这种现象的机制尚未被探索。不同种族和民族之间的饮食差异以及药物代谢或乙酰化基因的多态性变异尚未得到充分的分类。确定种族和族裔群体之间的遗传和环境因素将为观察到的流行病学数据提供一些见解,并为更好地了解结直肠癌的控制和发展提供机会。
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