Sharma Shikha, Rajaram Shalini, Sharma Tusha, Goel Neerja, Agarwal Sarla, Banerjee Basu Dev
Department of Obstetrics and Gynaecology, University College of Medical Sciences and Guru Teg Bahadur Hospital Shahdara, Delhi, India.
Department of Biochemistry, University College of Medical Sciences and Guru Teg Bahadur Hospital Shahdara, Delhi, India.
Int J Biochem Mol Biol. 2014 May 15;5(1):1-10. eCollection 2014.
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.
卵巢癌是一种隐匿的杀手,因为大多数患者症状不具特异性,通常在疾病晚期才出现。它是由某些基因改变和突变引起的,即奠基者突变,BRCA1基因中的187delAG和5385insC以及BRCA2基因中的6174delT,这些与特定家族病史相关。这些高外显率的易感基因约占包含2例或更多卵巢癌病例家族的一半,但在家族性额外恶性肿瘤风险中所占比例不到40%。其余风险可能归因于单核苷酸多态性(SNP),即DNA序列中的单碱基变化,在给定位置通常有两种可能的核苷酸替代。对30名经组织学证实为上皮性卵巢癌的女性进行了初步研究,并对她们进行了详细的基因分析。使用基于突变位点上下游200 bp区域设计的引物,对BRCA1和BRCA2基因上的奠基者突变区域进行扩增和测序。在BRCA1基因中鉴定出5个序列变异,其中3个新的序列变异在23名患者中发现,而在BRCA2基因中发现了1个新的序列变异。在任何受试者中均未发现BRCA1基因中的3个奠基者突变187delAG、5385insC以及BRCA2基因中的6174delT。