Author(s): Magalhães, J. F. ; Cortinhas, A. J. ; Albuquerque, C. M. ; Baptista, C. S. ; Ribeiro, R. ; Viegas, Carlos A. ; Matos, Augusto ; Machado, João ; Pires, Maria A. ; Pinto, Henrique Guedes ; Bessa, A. Martins ; Leitão, J. C. ; Bastos, E.
Date: 2013
Persistent ID: https://hdl.handle.net/1822/28177
Origin: RepositóriUM - Universidade do Minho
Subject(s): Interleukin-6; Polymorphism; Prostate cancer; Risk
Prostate cancer (PCa) is one of the most commonly diagnosed internal malignancies affecting men. Due to the important roles of IL-6 in different physiological and pathophysiological processes,IL-6polymorphisms may modulate PCa risk.IL-6−174 G>C (rs 1800795, also designated −236 G>C) and −636 G>C (rs 1800796, also designated −572 G>C) promoter polymorphisms have been implicated in PCa susceptibility, albeit still controversial. A literature search using PubMed and Highwire databases was conducted, resulting in eight case–control studies concerning theIL-6−174 G>C polymorphism (11,613 PCa cases and 13,992 controls) and four case–control publications regarding theIL-6−636 G>C polymorphism (1,941 PCa cases and 3,357 controls). In order to derive a more precise estimation, a meta-analysis based upon these selected case–control studies was performed. There was no significant association betweenIL-6−174 G>C polymorphism and PCa increased risk. Nevertheless, the presence of allele C and the CC genotype were statistically significantly associated with decreased PCa risk in the overall analysis forIL-6−636 G>C polymorphism. Additional studies in larger samples and analyses of functional repercussions of these SNPs in prostate tumor cells are necessary to validate these findings.
