BRCA1和BRCA2基因突变在印度人群上皮性卵巢癌中的作用:一项初步研究

International journal of biochemistry and molecular biology Pub Date : 2014-05-15 eCollection Date: 2014-01-01
Shikha Sharma, Shalini Rajaram, Tusha Sharma, Neerja Goel, Sarla Agarwal, Basu Dev Banerjee
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引用次数: 0

摘要

卵巢癌是一个无声的杀手,因为大多数患者没有特异性症状,通常出现在疾病的晚期。它的发生是由于某些遗传改变和突变,即BRCA1的始创突变,187delAG和5385insC, BRCA2的6174delT,这些与特定的家族史有关。这些高渗透的易感基因导致了大约一半有2个或2个以上卵巢癌病例的家庭,占家族过度恶性肿瘤风险的不到40%。剩余的风险可能是由于单核苷酸多态性(SNPs),这是DNA序列中单个碱基的变化,通常在给定位置上有两个可能的核苷酸替代。初步研究涉及30名组织学证实为上皮性卵巢癌的妇女,并对她们进行了详细的基因分析。利用基于突变位点上下游200 bp区域设计的引物,对BRCA1和BRCA2的始创突变区域进行扩增和测序。鉴定出BRCA1的5个序列变异,其中在23例患者中发现了3个新的序列变异,而在BRCA2中发现了1个新的序列变异。BRCA1中的三个始创突变187delAG、5385insC和BRCA2中的6174delT未在任何受试者中发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Ovarian cancer is a silent killer as most patients have non-specific symptoms and usually present in advanced stage of the disease. It occurs due to certain genetic alterations and mutations namely founder mutations, 187delAG and 5385insC in BRCA1 and 6174delT in BRCA2 which are associated with specific family histories. These highly penetrant susceptibility genes responsible for approximately half of families containing 2 or more ovarian cancer cases account for less than 40% of the familial excess malignancy risk. The remaining risk may be due to single nucleotide polymorphisms (SNPs) which are single base change in a DNA sequence with usual alternatives of two possible nucleotides at a given position. Preliminary study involving 30 women with histologically proven epithelial ovarian cancer was conducted and their detailed genetic analysis was carried out. Regions of founder mutations on BRCA1 and BRCA2 were amplified and sequenced using primers designed based on 200 bp upstream and downstream regions of the mutation sites. Five sequence variants in BRCA1 were identified of which three novel sequence variants were found in 23 patients while in BRCA2, one novel sequence variant was found. The three founder mutations 187delAG, 5385insC in BRCA1 and 6174delT in BRCA2 were not seen in any of the subjects.

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