Department of Health Studies, University of Chicago, 5841 South Maryland Avenue, MC 2007, Chicago, IL 60637, USA.
Carcinogenesis. 2012 Apr;33(4):835-40. doi: 10.1093/carcin/bgs093. Epub 2012 Feb 22.
Multiple breast cancer susceptibility loci have been identified in genome-wide association studies (GWAS) in populations of European and Asian ancestry using array chips optimized for populations of European ancestry. It is important to examine whether these loci are associated with breast cancer risk in women of African ancestry. We evaluated 25 single nucleotide polymorphisms (SNPs) at 19 loci in a pooled case-control study of breast cancer, which included 1509 cases and 1383 controls. Cases and controls were enrolled in Nigeria, Barbados and the USA; all women were of African ancestry. We found significant associations for three SNPs, which were in the same direction and of similar magnitude as those reported in previous fine-mapping studies in women of African ancestry. The allelic odds ratios were 1.24 [95% confidence interval (CI): 1.04-1.47; P = 0.018] for the rs2981578-G allele (10q26/FGFR2), 1.34 (95% CI: 1.10-1.63; P = 0.0035) for the rs9397435-G allele (6q25) and 1.12 (95% CI: 1.00-1.25; P = 0.04) for the rs3104793-C allele (16q12). Although a significant association was observed for an additional index SNP (rs3817198), it was in the opposite direction to prior GWAS studies. In conclusion, this study highlights the complexity of applying current GWAS findings across racial/ethnic groups, as none of GWAS-identified index SNPs could be replicated in women of African ancestry. Further fine-mapping studies in women of African ancestry will be needed to reveal additional and causal variants for breast cancer.
在使用针对欧洲人群优化的基因芯片进行的全基因组关联研究(GWAS)中,已经在欧洲和亚洲人群中发现了多个乳腺癌易感基因座。重要的是要检查这些基因座是否与非洲裔女性的乳腺癌风险相关。我们评估了 19 个基因座的 25 个单核苷酸多态性(SNP),这些 SNP 来自乳腺癌的病例对照研究,该研究包括 1509 例病例和 1383 例对照。病例和对照均来自尼日利亚、巴巴多斯和美国;所有女性均为非洲裔。我们发现了三个 SNP 的显著关联,这些 SNP 的方向和大小与以前在非洲裔女性中的精细映射研究报告的一致。等位基因比值比为 1.24(95%置信区间[CI]:1.04-1.47;P=0.018),rs2981578-G 等位基因(10q26/FGFR2),rs9397435-G 等位基因(6q25)为 1.34(95% CI:1.10-1.63;P=0.0035),rs3104793-C 等位基因(16q12)为 1.12(95% CI:1.00-1.25;P=0.04)。尽管观察到另一个索引 SNP(rs3817198)存在显著关联,但它与先前的 GWAS 研究方向相反。总之,本研究强调了将当前的 GWAS 研究结果应用于不同种族/民族群体的复杂性,因为在非洲裔女性中,没有一个 GWAS 确定的索引 SNP 可以被复制。需要对非洲裔女性进行进一步的精细映射研究,以揭示乳腺癌的其他和因果变异。