Ruiz-Narváez Edward A, Sucheston-Campbell Lara, Bensen Jeannette T, Yao Song, Haddad Stephen, Haiman Christopher A, Bandera Elisa V, John Esther M, Bernstein Leslie, Hu Jennifer J, Ziegler Regina G, Deming Sandra L, Olshan Andrew F, Ambrosone Christine B, Palmer Julie R, Lunetta Kathryn L
Slone Epidemiology Center, Boston University, Boston MA, USA.
College of Pharmacy, The Ohio State University, ColumbusOH, USA; College of Veterinary Medicine, The Ohio State University, ColumbusOH, USA.
Front Genet. 2016 Sep 21;7:170. doi: 10.3389/fgene.2016.00170. eCollection 2016.
Recent genetic admixture coupled with striking differences in incidence of estrogen receptor (ER) breast cancer subtypes, as well as severity, between women of African and European ancestry, provides an excellent rationale for performing admixture mapping in African American women with breast cancer risk. We performed the largest breast cancer admixture mapping study with in African American women to identify novel genomic regions associated with the disease. We conducted a genome-wide admixture scan using 2,624 autosomal ancestry informative markers (AIMs) in 3,629 breast cancer cases (including 1,968 ER-positive, 1093 ER-negative, and 601 triple-negative) and 4,658 controls from the African American Breast Cancer Epidemiology and Risk (AMBER) Consortium, a collaborative study of four large geographically different epidemiological studies of breast cancer in African American women. We used an independent case-control study to test for SNP association in regions with genome-wide significant admixture signals. We found two novel genome-wide significant regions of excess African ancestry, 4p16.1 and 17q25.1, associated with ER-positive breast cancer. Two regions known to harbor breast cancer variants, 10q26 and 11q13, were also identified with excess of African ancestry. Fine-mapping of the identified genome-wide significant regions suggests the presence of significant genetic associations with ER-positive breast cancer in 4p16.1 and 11q13. In summary, we identified three novel genomic regions associated with breast cancer risk by ER status, suggesting that additional previously unidentified variants may contribute to the racial differences in breast cancer risk in the African American population.
近期的基因混合现象,以及非洲裔和欧洲裔女性在雌激素受体(ER)乳腺癌亚型的发病率和严重程度上存在的显著差异,为在有乳腺癌风险的非裔美国女性中进行混合映射提供了绝佳的理论依据。我们开展了针对非裔美国女性的最大规模乳腺癌混合映射研究,以确定与该疾病相关的新基因组区域。我们使用2624个常染色体祖先信息标记(AIM),对来自非裔美国乳腺癌流行病学与风险(AMBER)联盟的3629例乳腺癌病例(包括1968例ER阳性、1093例ER阴性和601例三阴性)和4658例对照进行了全基因组混合扫描。AMBER联盟是一项对非洲裔美国女性乳腺癌进行的四项大型地理上不同的流行病学研究的合作项目。我们使用一项独立的病例对照研究,来检验全基因组显著混合信号区域中的单核苷酸多态性(SNP)关联。我们发现了两个新的全基因组显著的非洲祖先血统过量区域,4p16.1和17q25.1,与ER阳性乳腺癌相关。还发现了两个已知含有乳腺癌变异的区域,10q26和11q13,也有过量的非洲祖先血统。对已确定的全基因组显著区域进行精细定位表明,在4p16.1和11q13中存在与ER阳性乳腺癌的显著遗传关联。总之,我们通过ER状态确定了三个与乳腺癌风险相关的新基因组区域,这表明其他先前未识别的变异可能导致非裔美国人群乳腺癌风险的种族差异。