Department of Molecular Medicine, Institute for Experimental Medicine Research, Istanbul University, Vakif Gureba cad, 34390 Capa, Istanbul, Turkey.
Mol Biol Rep. 2011 Jun;38(5):3481-6. doi: 10.1007/s11033-010-0458-7. Epub 2010 Nov 24.
In this study, we aimed to investigate a possible association of the COX-2 polymorphisms (-765G→C and -1195A→G) and with the risk of developing epithelial ovarian carcinoma (EOC). COX-2 gene polymorphisms was investigated in 111 healthy women and 57 patients with EOC. Individuals who had -765 CG, -1195 AA genotype, and -765 C allele had increased risk for ovarian carcinoma (P < 0.01) and individuals with -765 GG, -1195 AG genotypes and -1195 G allele seem to be protected from ovarian carcinoma (P < 0.01). Haplotype analysis confirmed the association of COX-2 gene variants with ovarian carcinoma and revealed that the frequencies of -765C: -1195A haplotype frequencies was significantly higher in patients as compared with those of controls (P = 0.048). We state that there appears to be a modulating role for the COX-2 -1195A→G and -765G→C polymorphisms in the development of EOC. To the best of our knowledge, this is the first study to show such an association.
在这项研究中,我们旨在研究 COX-2 多态性(-765G→C 和-1195A→G)与上皮性卵巢癌(EOC)发病风险的可能关联。我们在 111 名健康女性和 57 名 EOC 患者中研究了 COX-2 基因多态性。-765 CG、-1195 AA 基因型和-765 C 等位基因的个体患卵巢癌的风险增加(P<0.01),而-765 GG、-1195 AG 基因型和-1195 G 等位基因的个体似乎对卵巢癌有保护作用(P<0.01)。单体型分析证实了 COX-2 基因变异与卵巢癌的关联,并表明与对照组相比,患者中-765C:-1195A 单体型频率明显更高(P=0.048)。我们认为 COX-2-1195A→G 和-765G→C 多态性在 EOC 的发生中似乎具有调节作用。据我们所知,这是第一项表明这种关联的研究。