Author/Authors :
Çayan, Filiz Department of Obstetrics and Gynecology - Faculty of Medicine - Mersin University, Mersin, Turkey , Dilek, Saffet Department of Obstetrics and Gynecology - Faculty of Medicine - Mersin University, Mersin, Turkey , Gen, Ramazan Department of Internal Medicine - Faculty of Medicine - Mersin University, Mersin, Turkey , Akbay, Esen Department of Internal Medicine - Faculty of Medicine - Mersin University, Mersin, Turkey , Ateş, Nurcan Aras Department of Medical Biology and Genetics - Faculty of Medicine - Mersin University, Mersin, Turkey , Ayaz, Lokman Department of Biochemistry - Faculty of Medicine - Mersin University, Mersin, Turkey
Abstract :
Objective: The insulin receptor substrate (IRS) proteins have been implicated in contributing to all stages of tumorigenesis in many cancers, from initiat- ing events to metastatic progression. In this study, we aimed to evaluate the association of IRS-2 gene polymorphism with ovarian cancer. Material and Methods: The study group consisted of 185 women: 45 women with ovarian cancer and 140 control subjects. All the patients with ovarian cancer were primarily treated by surgical intervention. Genetic polymorphism of IRS-2 G1057D was detected by using polymerase chain reaction (PCR)- based restriction fragment-length polymorphism (RFLP). Results: For IRS-2 G1057D polymorphism, the frequencies of GG, GD and DD genotypes were 60%, 33.3%, and 6.7%, respectively in the ovarian cancer cases and 53.6%, 38.6% and 7.9 % in controls. The risk for ovarian cancer was not significantlydifferent in the individuals with the IRS-2 DD genotype compared to the GG genotype (95% CI: 0.203-3.04, P: 0.787). Also, there was no association between carriage of the D allele and ovarian cancer risk. We found no significant difference between the genotypes in the ovarian cancer group and control group (P:0.545). Conclusion: These results do not support an association between carriage of the G1057D variant of IRS-2 gene and ovarian cancer.
Keywords :
Insulin receptor substrate , 2 gene polymorphism , ovarian cancer , G1057D variation