Association of common BRCA1 variants with predisposition to breast tumors in Pakistan

IF 1 4区 生物学 Q4 GENETICS & HEREDITY
Ayesha Siddique, Warda Fatima, Naeem Shahid
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引用次数: 0

Abstract

BRCA1 variants are extensively associated with increased risk of breast cancer. Early detection and screening of variants is still rare in developing countries. Here, we investigated six BRCA1 variants in 300 subjects from Pakistani population using tetra amplification-refractory mutation system (T-ARMS) PCR. Our results indicate significant association of BRCA1 variants rs8176237 (AA; OR 8.2, 95% CI 3.02–22.64, p < 0.0001), rs1060915 (CC; OR 4.29, 95% CI 1.94–9.48, p = 0.0003), and rs799912 (TT; OR 3.16, 95% CI 1.44–6.94, p = 0.004) with up to 8-fold increased odds of breast cancer under recessive model. Furthermore, BRCA1 haplotypes AGCACG and AGCCCT were associated with up to 18% breast cancer cases (p < 0.05). Additionally, we found association of these variants with up to 11-fold increased odds of benign breast tumors. Linkage disequilibrium (LD) block-wise analysis revealed haplotypes GCAC and ATAC were associated with significantly increased risk. To our knowledge, this is the first study that identifies the association of these BRCA1 variants with breast tumors in Pakistani population. In conclusion, BRCA1 variants investigated in the present study are associated with high odds of benign- and malignant breast tumors. Studies with bigger sample size may help early detection and screening to reduce the odds of breast cancer.

Abstract Image

巴基斯坦常见BRCA1变异与乳腺肿瘤易感性的关系
BRCA1变异与乳腺癌风险增加广泛相关。在发展中国家,早期发现和筛查变异仍然很罕见。在这里,我们使用四倍扩增-难解突变系统(T-ARMS) PCR研究了300名来自巴基斯坦人群的6种BRCA1变异。我们的研究结果表明BRCA1变异rs8176237 (AA;OR 8.2, 95% CI 3.02-22.64, p <0.0001), rs1060915 (CC;OR 4.29, 95% CI 1.94-9.48, p = 0.0003), rs799912 (TT;OR 3.16, 95% CI 1.44-6.94, p = 0.004),隐性模型下乳腺癌的几率增加8倍。此外,BRCA1单倍型AGCACG和AGCCCT与高达18%的乳腺癌病例相关(p <0.05)。此外,我们发现这些变异与良性乳腺肿瘤的几率增加了11倍。连锁不平衡(LD)块分析显示,单倍型GCAC和ATAC的风险显著增加。据我们所知,这是首次在巴基斯坦人群中确定这些BRCA1变异与乳腺肿瘤之间关系的研究。总之,本研究中研究的BRCA1变异与良性和恶性乳腺肿瘤的高发生率相关。更大样本量的研究可能有助于早期发现和筛查,以降低患乳腺癌的几率。
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来源期刊
Annals of Human Genetics
Annals of Human Genetics 生物-遗传学
CiteScore
4.20
自引率
0.00%
发文量
34
审稿时长
3 months
期刊介绍: Annals of Human Genetics publishes material directly concerned with human genetics or the application of scientific principles and techniques to any aspect of human inheritance. Papers that describe work on other species that may be relevant to human genetics will also be considered. Mathematical models should include examples of application to data where possible. Authors are welcome to submit Supporting Information, such as data sets or additional figures or tables, that will not be published in the print edition of the journal, but which will be viewable via the online edition and stored on the website.
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