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非洲裔乳腺癌患者中 BRCA1 和 BRCA2 基因突变的复发性。

Recurrent BRCA1 and BRCA2 mutations in breast cancer patients of African ancestry.

机构信息

Center for Clinical Cancer Genetics and Global Health, Department of Medicine, The University of Chicago, Chicago, IL, USA.

出版信息

Breast Cancer Res Treat. 2012 Jul;134(2):889-94. doi: 10.1007/s10549-012-2136-z. Epub 2012 Jun 28.

Abstract

Recurrent mutations constituted nearly three quarters of all BRCA1 mutations and almost half of all BRCA2 mutations identified in the first cohort of the Nigerian Breast Cancer Study. To further characterize breast/ovarian cancer risks associated with BRCA1/BRCA2 mutations in the African diaspora, we genotyped recurrent mutations among Nigerian, African American, and Barbadian breast cancer patients. A replication cohort of 356 Nigerian breast cancer patients was genotyped for 12 recurrent BRCA1/2 mutant alleles (Y101X, 1742insG, 4241delTG, M1775R, 4359insC, C64Y, 1623delTTAAA, Q1090X, and 943ins10 from BRCA1, and 1538delAAGA, 2630del11, and 9045delGAAA from BRCA2) by means of SNaPshot followed by direct sequencing or by direct sequencing alone. In addition, 260 African Americans and 118 Barbadians were genotyped for six of the recurrent BRCA1 mutations by SNaPshot assay. Of all the BRCA1/2 recurrent mutations we identified in the first cohort, six were identified in 11 patients in the replication study. These mutation carriers constitute 3.1 % [95 % Confidence Interval (CI) 1.6-5.5 %] of the replication cohort. By comparison, 6.9 % (95 % CI 4.7-9.7 %) of the discovery cohort carried BRCA1/2 recurrent mutations. For the subset of recurrent mutations we tested in breast cancer cases from Barbados or the United States, only two 943ins10 carriers were identified in African Americans. Nigerian breast cancer patients from Ibadan carry a broad and unique spectrum of BRCA1/2 mutations. Our data suggest that BRCA1/2 mutation testing limited to recurrent mutations is not sufficient to understand the BRCA1/2-associated breast cancer risk in African populations in the diaspora. As the cost of Sanger sequencing is considerably reduced, deploying innovative technologies such as high throughput DNA sequencing of BRCA1/2 and other cancer susceptibility genes will be essential for identifying high-risk individuals and families to reduce the burden of aggressive early onset breast cancer in low-resource settings.

摘要

在尼日利亚乳腺癌研究的第一队列中发现,反复出现的突变几乎构成了所有 BRCA1 突变的四分之三,几乎占所有 BRCA2 突变的一半。为了进一步描述非洲侨民中 BRCA1/BRCA2 突变与乳腺癌/卵巢癌风险的关系,我们对尼日利亚、非裔美国人和巴巴多斯乳腺癌患者中的反复出现的突变进行了基因分型。对 356 名尼日利亚乳腺癌患者的复制队列进行了 12 种 BRCA1/2 突变等位基因(来自 BRCA1 的 Y101X、1742insG、4241delTG、M1775R、4359insC、C64Y、1623delTTAAA、Q1090X 和 943ins10,以及来自 BRCA2 的 1538delAAGA、2630del11 和 9045delGAAA)的基因分型,方法是通过 SNaPshot 进行直接测序或单独进行直接测序。此外,通过 SNaPshot 检测对 260 名非裔美国人和 118 名巴巴多斯人进行了六种常见 BRCA1 突变的基因分型。在我们在第一队列中确定的所有 BRCA1/2 反复出现的突变中,有 6 个在复制研究的 11 名患者中发现。这些突变携带者构成了复制队列的 3.1%[95%置信区间(CI)1.6-5.5%]。相比之下,发现队列中有 6.9%(95%CI 4.7-9.7%)的人携带 BRCA1/2 反复出现的突变。对于我们在巴巴多斯或美国的乳腺癌病例中测试的反复出现的突变亚组,仅在非裔美国人中发现了两个 943ins10 携带者。伊巴丹的尼日利亚乳腺癌患者携带广泛而独特的 BRCA1/2 突变谱。我们的数据表明,仅对反复出现的突变进行 BRCA1/2 突变检测不足以了解侨民中非洲人群的 BRCA1/2 相关乳腺癌风险。随着桑格测序成本的大幅降低,部署高通量 BRCA1/2 和其他癌症易感性基因的 DNA 测序等创新技术对于确定高危个体和家庭以降低资源匮乏环境中侵袭性早发性乳腺癌的负担至关重要。

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