Liede Alexander, Narod Steven A
Centre for Research in Women's Health, University of Toronto, Toronto, Ontario, Canada.
Hum Mutat. 2002 Dec;20(6):413-24. doi: 10.1002/humu.10154.
Ethnic differences in cancer incidence and mortality result from differences in genetic and epidemiologic risk factors. Mutations in BRCA1 and BRCA2 account for a small proportion of all breast cancer cases, but for a much higher proportion of cases with a strong family history of breast or ovarian cancer. Germline mutations in BRCA1 and BRCA2 have been identified in individuals of many races and ethnic groups and the frequency of mutations varies between these groups. Some of the differences in cancer risk between populations may be the result of founder mutations in these genes. The cost and time required for mutation analysis are reduced considerably when founder mutations are identified for a specific ethnic group. The BRCA2 999del5 mutation in Iceland and three BRCA mutations in Ashkenazi Jews are well characterized. However, considerably less is known about the contribution of mutations in the BRCA1 and BRCA2 genes outside of European groups. Studies conducted on the Asian populations described here have expanded our current knowledge of genetic susceptibility and its contribution to breast and ovarian cancer rates in Asian populations.
癌症发病率和死亡率的种族差异源于遗传和流行病学风险因素的不同。BRCA1和BRCA2基因的突变在所有乳腺癌病例中所占比例较小,但在有强烈乳腺癌或卵巢癌家族史的病例中所占比例要高得多。在许多种族和族裔群体的个体中都发现了BRCA1和BRCA2基因的种系突变,而且这些群体之间的突变频率有所不同。人群之间癌症风险的一些差异可能是这些基因中奠基者突变的结果。当为特定种族群体鉴定出奠基者突变时,突变分析所需的成本和时间会大幅降低。冰岛的BRCA2 999del5突变以及德系犹太人中的三种BRCA突变已得到充分表征。然而,对于欧洲群体以外的BRCA1和BRCA2基因突变的贡献了解得要少得多。在此描述的针对亚洲人群开展的研究扩展了我们目前对遗传易感性及其对亚洲人群乳腺癌和卵巢癌发病率贡献的认识。