Department of Epidemiology, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.
Prostate. 2013 May;73(7):734-42. doi: 10.1002/pros.22617. Epub 2012 Nov 9.
While several studies showed that selenium may prevent prostate cancer (PCa), few studies have evaluated variation in selenoenzyme genes in relation to PCa risk and survival.
We studied common variants in seven selenoenzymes genes in relation to risk of PCa and PCa-specific mortality (PCSM). In a population-based case-control study of men of European ancestry (1,309 cases, 1,266 controls), we evaluated 35 common, tagging single nucleotide polymorphisms (SNPs) in GPX1 (n = 2), GPX2 (n = 4), GPX3 (n = 6), GPX4 (n = 6), SEP15 (n = 4), SEPP1 (n = 6), and TXNRD1 (n = 7) in relation to PCa risk, and among cases, associations between these variants and risk of PCSM. We used logistic regression and Cox proportional hazards regression to estimate the relative risk of PCa and PCSM, respectively.
Of the SNPs examined, only GPX1 rs3448 was associated with overall PCa risk with an odds ratio of 0.62 for TT versus CC (95% confidence interval, 0.44-0.88). SNPs in GPX2, GPX3, GPX4, SEP15, and SEPP1 had different risk estimates for PCa in subgroups based on stage and grade. We observed associations between SNPs in GPX4, and TXNRD1 and risk of PCSM. None of these associations, however, remained significant after adjustment for multiple comparisons.
We found evidence that genetic variation in a subset of selenoenzyme genes may alter risk of PCa and PCSM. These results need validation in additional subsets.
虽然几项研究表明硒可能预防前列腺癌(PCa),但很少有研究评估硒酶基因的变异与 PCa 风险和生存的关系。
我们研究了七个硒酶基因中的常见变异与 PCa 风险和 PCa 特异性死亡率(PCSM)的关系。在一项基于人群的欧洲裔男性病例对照研究中(1309 例病例,1266 例对照),我们评估了 GPX1(n=2)、GPX2(n=4)、GPX3(n=6)、GPX4(n=6)、SEP15(n=4)、SEPP1(n=6)和 TXNRD1(n=7)中 35 个常见的标记单核苷酸多态性(SNP)与 PCa 风险的关系,并在病例中,这些变体与 PCSM 风险之间的关联。我们使用逻辑回归和 Cox 比例风险回归分别估计 PCa 和 PCSM 的相对风险。
在所检查的 SNP 中,只有 GPX1 rs3448 与总体 PCa 风险相关,TT 与 CC 的比值比为 0.62(95%置信区间,0.44-0.88)。GPX2、GPX3、GPX4、SEP15 和 SEPP1 中的 SNP 根据阶段和分级,对 PCa 的风险有不同的估计值。我们观察到 GPX4 和 TXNRD1 中的 SNP 与 PCSM 的风险之间存在关联。然而,在进行多次比较调整后,这些关联均不再显著。
我们发现了证据表明,硒酶基因亚组中的遗传变异可能改变 PCa 和 PCSM 的风险。这些结果需要在其他亚组中进行验证。