Laboratory of Biochemistry-CHU Farhat Hached, Sousse 4000, Tunisia.
Pathol Oncol Res. 2011 Jun;17(2):295-9. doi: 10.1007/s12253-010-9314-2. Epub 2010 Nov 3.
MUC16 plays an important role in epithelial ovarian cancer. In this paper, we studied the association between two tags SNPs of MUC16 and the risk of epithelial ovarian cancer. We aimed also to test the association between these tags SNPs and elevated level of the protein CA125. We analyzed a collection of 117 cases. Forty-one samples of patients with epithelial ovarian cancer and 76 samples from Tunisian volunteers were genotyped for two synonymous coding tags SNPs of the MUC16 gene (rs1596797, A/C and rs2547065, C/G) using polymerase chain reaction and sequencing. For the rs1596797 SNP, there was no significant difference in genotype distribution, a rare variation observed in only one patient. For the polymorphism rs2547065, mean CA125 levels were 24 and 78 UI/ml in patients with GG and GC genotypes versus 230 UI/ml in patients with CC genotype (P = 0.36). Compared to the C/C genotype, the 'G' allele (C/G+G/G genotypes) did not significantly modified the risk of developing epithelial ovarian cancer (OR = 0.43; 95% CI). As for the polymorphism rs1596797, compared to the C/C genotype, the 'A' allele (C/A+A/A genotypes) did not significantly modified the risk of developing epithelial ovarian cancer (OR = 881.7; 95% CI). MUC16 gene polymorphisms selected in this study are neither involved in genetic predisposition to epithelial ovarian cancer nor associated with CA125 level.
MUC16 在卵巢上皮性癌中起重要作用。本研究旨在探讨 MUC16 两个标签 SNP 与上皮性卵巢癌发病风险的关系,以及这些标签 SNP 与蛋白 CA125 水平升高的关系。我们分析了 117 例标本。41 例上皮性卵巢癌患者和 76 例来自突尼斯志愿者的样本,采用聚合酶链反应和测序技术对 MUC16 基因的两个同义编码标签 SNP(rs1596797,A/C 和 rs2547065,C/G)进行基因分型。rs1596797 基因型分布无显著差异,仅 1 例患者存在罕见变异。对于 rs2547065 多态性,GG 和 GC 基因型患者的 CA125 水平均值分别为 24 和 78 UI/ml,而 CC 基因型患者为 230 UI/ml(P = 0.36)。与 C/C 基因型相比,G 等位基因(C/G+G/G 基因型)并未显著改变上皮性卵巢癌的发病风险(OR = 0.43;95%CI)。对于 rs1596797 多态性,与 C/C 基因型相比,A 等位基因(C/A+A/A 基因型)也未显著改变上皮性卵巢癌的发病风险(OR = 881.7;95%CI)。本研究选择的 MUC16 基因多态性既不参与上皮性卵巢癌的遗传易感性,也与 CA125 水平无关。