Weill Cornell Medicine, New York, NY.
Henry Ford Cancer Institute, Detroit, MI.
Ann Surg. 2019 Sep;270(3):484-492. doi: 10.1097/SLA.0000000000003459.
To investigate subtype-specific risk of germline alleles associated with triple negative breast cancer (TNBC) in African ancestry populations.
Breast cancer (BC) mortality is higher in African American (AA) compared to White American (WA) women; this disparity is partly explained by 2-fold higher TNBC incidence.
We used a surgically maintained biospecimen cohort of 2884 BC cases. Subsets of the total (760 AA; 962 WA; 910 West African/Ghanaian; 252 East African/Ethiopian) were analyzed for genotypes of candidate alleles. A subset of 417 healthy controls were also genotyped, to measure associations with overall BC risk and TNBC.
TNBC frequency was highest in Ghanaian and AA cases (49% and 44% respectively; P < 0.0001) and lowest in Ethiopian and WA cases (17% and 24% respectively; P < 0.0001). TNBC cases had higher West African ancestry than non-TNBC (P < 0.0001). Frequency of the Duffy-null allele (rs2814778; an African ancestral variant adopted under selective pressure as protection against malaria) was associated with TNBC-specific risk (P < 0.0001), quantified West African Ancestry (P < 0.0001) and was more common in AA, Ghanaians, and TNBC cases. Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant.
West African ancestry is strongly correlated with TNBC status, as well as germline variants related to BC risk. The Duffy-null allele was associated with TNBC risk in our cohort.
探究与非裔人群三阴性乳腺癌(TNBC)相关的种系等位基因的亚型特异性风险。
非裔美国女性(AA)的乳腺癌(BC)死亡率高于白种美国女性(WA);这种差异部分归因于 TNBC 发病率高两倍。
我们使用了一个由 2884 例 BC 病例组成的手术维护生物样本队列。对总队列的亚组(760 例 AA;962 例 WA;910 例西非/加纳;252 例东非/埃塞俄比亚)进行了候选等位基因基因型分析。还对 417 例健康对照进行了基因分型,以衡量与总体 BC 风险和 TNBC 的关联。
加纳和 AA 病例的 TNBC 发生率最高(分别为 49%和 44%;P < 0.0001),而埃塞俄比亚和 WA 病例的 TNBC 发生率最低(分别为 17%和 24%;P < 0.0001)。TNBC 病例的西非血统比非 TNBC 病例更高(P < 0.0001)。Duffy 缺失等位基因(rs2814778;一种在选择压力下作为预防疟疾的保护而被采用的非洲祖先变体)的频率与 TNBC 特异性风险相关(P < 0.0001),量化了西非血统(P < 0.0001),并且在 AA、加纳人和 TNBC 病例中更为常见。此外,rs4849887 与总体 BC 风险显著相关,rs2363956 和 rs13000023 与 TNBC 特异性风险相关,尽管没有一个像 Duffy 缺失变体那样强。
西非血统与 TNBC 状态以及与 BC 风险相关的种系变异密切相关。在我们的队列中,Duffy 缺失等位基因与 TNBC 风险相关。