Kucukgergin C, Gokpinar M, Sanli O, Tefik T, Oktar T, Seckin S
Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Minerva Urol Nefrol. 2011 Sep;63(3):183-90.
The aim of this study was to investigate the association between GPx1 Pro198Leu polymorphism with the development and progression of prostate cancer (PCa) and evaluate whether smoking status and advanced age could modify this association.
A total of 134 PCa patients and 159 healthy control subjects with serum prostate specific antigen (PSA) levels <4 ng/mL and normal digital rectal examination (DRE) findings were enrolled in this prospectively designed study. PCA patients were classified as low (T1 or T2 and N0M0 stages) and high stage disease (T3 or T4 and N0M0 or N1 or M1 stages). GPx1 Pro198Leu polymorphism was determined using polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP). Logistic regression analysis was used to estimate odds ratios (OR) and 95% confidence intervals (95%CI).
Compared to the carriers of Pro/Pro genotype, subjects with the variant genotypes (Pro/Leu or Leu/Leu) had significantly higher risk of PCa. The Leu/Leu genotype was correlated with lower GPx activity among both controls and PCa patients. With respect to tumor stage, Leu/Leu genotype was more frequent in patients with high stage disease than those of low stage disease. In stratified analyses, although the variant Leu/Leu genotype was significantly associated with increased risk of PCa in older age, smoking did not alter this association.
The present data provide evidence that GPx1 Pro198Leu polymorphism may be associated with the development and progression of PCa and older ages may influence the association.between GPx1 Pro198Leu polymorphism and PCa.
本研究旨在探讨谷胱甘肽过氧化物酶1(GPx1)基因Pro198Leu多态性与前列腺癌(PCa)发生发展的相关性,并评估吸烟状态和高龄是否会改变这种相关性。
本前瞻性设计研究共纳入134例PCa患者和159例血清前列腺特异性抗原(PSA)水平<4 ng/mL且直肠指检(DRE)结果正常的健康对照者。PCa患者分为低分期(T1或T2且N0M0期)和高分期疾病(T3或T4且N0M0或N1或M1期)。采用聚合酶链反应(PCR)-限制性片段长度多态性(RFLP)方法测定GPx1基因Pro198Leu多态性。采用逻辑回归分析估计比值比(OR)和95%置信区间(95%CI)。
与Pro/Pro基因型携带者相比,具有变异基因型(Pro/Leu或Leu/Leu)的受试者患PCa的风险显著更高。Leu/Leu基因型在对照组和PCa患者中均与较低的GPx活性相关。就肿瘤分期而言,高分期疾病患者中Leu/Leu基因型的频率高于低分期疾病患者。在分层分析中,尽管变异的Leu/Leu基因型在老年患者中与PCa风险增加显著相关,但吸烟并未改变这种相关性。
目前的数据表明,GPx1基因Pro198Leu多态性可能与PCa的发生发展相关,高龄可能会影响GPx1基因Pro198Leu多态性与PCa之间的相关性。