Association between genetic polymorphisms of inflammatory response genes and the risk of ovarian cancer.

Abstract

Inflammation plays an important role in promoting ovarian tumorigenesis and cancer progression. However, the relationship between polymorphisms in inflammatory response genes and risk of ovarian cancer remains poorly understood. In this study, we investigated the association of PPARG Pro12Ala, IL6-174G/C, E-selectin S128R, NFKB1-94 ins/del, NFKBIA-826C/T, and ICAM-1 K469E polymorphisms with ovarian cancer risk in a Chinese population. Genotyping of the polymorphisms was performed on 687 cases and 687 controls employing the PCR-RFLP technique, and the logistic regression model was used to measure the risk association. A significantly increased risk association was observed for the heterozygous genotypes of PPARG [odds ratio (OR)=1.52, 95% confidence interval (CI)=1.01-2.29] and E-selectin (OR=1.77, 95% CI=1.07-2.93) polymorphisms, as well as the homozygous ins/ins genotype of NFKB1 polymorphism (OR=1.39, 95% CI=1.00-1.92). By contrast, ICAM-1 KE genotype was associated with a decreased ovarian cancer risk (OR=0.77, 95% CI=0.60-0.98). In addition, the NFKB1 del/del+NFKBIA TT combination was also found to be associated with a decreased ovarian cancer risk, with OR=0.12 (95% CI=0.01-0.95). The associations of the NFKB1 and ICAM-1 polymorphisms replicated the findings of previous reports, assuring the reliability of the results obtained. NFKB1 and ICAM-1 polymorphisms could serve as useful ovarian cancer risk prediction biomarkers for the Chinese population, while the utility of PPARG and E-selectin polymorphisms as biomarkers requires further confirmation in independent ovarian cancer cohorts.