Cyclooxygenase-2 gene and epithelial ovarian carcinoma risk

被引:10
作者
Cakmakoglu, Bedia Agachan [1 ]
Attar, Rukset [2 ]
Kahraman, Ozlem Timirci [1 ]
Dalan, Altay Burak [1 ]
Iyibozkurt, Ahmet Cem [3 ]
Karateke, Ates [4 ]
Attar, Erkut [3 ]
机构
[1] Istanbul Univ, Expt Med Res Inst, Dept Mol Med, TR-34390 Istanbul, Turkey
[2] Yeditepe Univ Hosp, Dept Obstet & Gynecol, Istanbul, Turkey
[3] Istanbul Univ, Istanbul Med Sch, Dept Obstet & Gynecol, TR-34390 Istanbul, Turkey
[4] Zeynep Kamil Res & Training Hosp, Istanbul, Turkey
关键词
Cox-2; Epithelial ovarian carcinoma; Polymorphism; NITRIC-OXIDE SYNTHASE; MESSENGER-RNA EXPRESSION; PROGNOSTIC-SIGNIFICANCE; COLORECTAL-CANCER; LUNG-CARCINOMA; GROWTH-FACTOR; POLYMORPHISM; ADENOCARCINOMAS; ANGIOGENESIS; ASSOCIATION;
D O I
10.1007/s11033-010-0458-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:3481 / 3486
页数:6
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