Epidemiology Research Program, American Cancer Society, Atlanta, Georgia, USA.
PLoS Genet. 2013;9(3):e1003173. doi: 10.1371/journal.pgen.1003173. Epub 2013 Mar 27.
Common genetic variants contribute to the observed variation in breast cancer risk for BRCA2 mutation carriers; those known to date have all been found through population-based genome-wide association studies (GWAS). To comprehensively identify breast cancer risk modifying loci for BRCA2 mutation carriers, we conducted a deep replication of an ongoing GWAS discovery study. Using the ranked P-values of the breast cancer associations with the imputed genotype of 1.4 M SNPs, 19,029 SNPs were selected and designed for inclusion on a custom Illumina array that included a total of 211,155 SNPs as part of a multi-consortial project. DNA samples from 3,881 breast cancer affected and 4,330 unaffected BRCA2 mutation carriers from 47 studies belonging to the Consortium of Investigators of Modifiers of BRCA1/2 were genotyped and available for analysis. We replicated previously reported breast cancer susceptibility alleles in these BRCA2 mutation carriers and for several regions (including FGFR2, MAP3K1, CDKN2A/B, and PTHLH) identified SNPs that have stronger evidence of association than those previously published. We also identified a novel susceptibility allele at 6p24 that was inversely associated with risk in BRCA2 mutation carriers (rs9348512; per allele HR = 0.85, 95% CI 0.80-0.90, P = 3.9 × 10(-8)). This SNP was not associated with breast cancer risk either in the general population or in BRCA1 mutation carriers. The locus lies within a region containing TFAP2A, which encodes a transcriptional activation protein that interacts with several tumor suppressor genes. This report identifies the first breast cancer risk locus specific to a BRCA2 mutation background. This comprehensive update of novel and previously reported breast cancer susceptibility loci contributes to the establishment of a panel of SNPs that modify breast cancer risk in BRCA2 mutation carriers. This panel may have clinical utility for women with BRCA2 mutations weighing options for medical prevention of breast cancer.
常见的遗传变异导致 BRCA2 突变携带者的乳腺癌风险存在差异;迄今为止,所有这些变异都是通过基于人群的全基因组关联研究(GWAS)发现的。为了全面鉴定 BRCA2 突变携带者的乳腺癌风险修饰基因座,我们对一项正在进行的 GWAS 发现研究进行了深入复制。使用与 140 万个 SNP 的推断基因型相关的乳腺癌关联的排名 P 值,选择了 19029 个 SNP,并设计将其包含在一个定制的 Illumina 阵列中,该阵列共包含 211155 个 SNP,作为一个多联合项目的一部分。来自 47 项研究的 3881 名乳腺癌患者和 4330 名无乳腺癌的 BRCA2 突变携带者的 DNA 样本,属于 BRCA1/2 修饰因子调查员联合组织,经基因分型并可用于分析。我们在这些 BRCA2 突变携带者中复制了先前报道的乳腺癌易感等位基因,并在几个区域(包括 FGFR2、MAP3K1、CDKN2A/B 和 PTHLH)鉴定出比先前报道的具有更强关联证据的 SNP。我们还在 6p24 上鉴定出一个新的易感等位基因,该等位基因与 BRCA2 突变携带者的风险呈负相关(rs9348512;每个等位基因的 HR=0.85,95%CI 0.80-0.90,P=3.9×10(-8))。该 SNP 无论是在一般人群中还是在 BRCA1 突变携带者中,均与乳腺癌风险无关。该基因座位于一个包含 TFAP2A 的区域内,该基因编码一种转录激活蛋白,与几个肿瘤抑制基因相互作用。本报告鉴定了第一个特定于 BRCA2 突变背景的乳腺癌风险基因座。对新的和先前报道的乳腺癌易感基因座的全面更新有助于建立一个 SNP 面板,该面板可改变 BRCA2 突变携带者的乳腺癌风险。该面板可能对权衡 BRCA2 突变女性进行乳腺癌医学预防的选择具有临床应用价值。