Rybicki Benjamin A, Neslund-Dudas Christine, Nock Nora L, Schultz Lonni R, Eklund Ludmila, Rosbolt James, Bock Cathryn H, Monaghan Kristin G
Department of Biostatistics and Research Epidemiology, Henry Ford Health System, Detroit, MI 48202, USA.
Cancer Detect Prev. 2006;30(5):412-22. doi: 10.1016/j.cdp.2006.09.004. Epub 2006 Oct 25.
Variation in the glutathione S-transferase (GSTP1) gene and occupational polycyclic aromatic hydrocarbons (PAH) exposure are putative prostate cancer risk factors. An Ile/Val polymorphism in codon 105 of GSTP1 affects its enzymatic activity toward PAH detoxification, a possible mechanism in prostate carcinogenesis.
To determine whether the GSTP1 Ile105Val polymorphism modifies prostate cancer risk associated with occupational PAH exposure, we studied 637 prostate cancer cases and 244 controls of White and African-American race from the Henry Ford Health System in Detroit, Michigan. Occupational exposure to PAH from wood, petroleum, coal or other sources through respiratory and cutaneous routes was retrospectively assessed by expert review of job histories. The association of occupational PAH exposure and GSTP1 Ile105Val polymorphism with prostate cancer was tested in multiple logistic regression models adjusting for potential confounders. Cases were over sampled compared with controls to evaluate gene-environment interaction with the statistically efficient case-only analytic approach.
Neither carriage of the GSTP1 Val(105) variant allele nor occupational PAH exposure was significantly associated with prostate cancer. However, case-only analyses revealed that carriage of the GSTP1 Val(105) variant allele was associated with increasing levels of occupational respiratory PAH exposures from any source and from petroleum (trend test p=0.01 for both). The GSTP1 Val(105) allele was observed most frequently in cases in the highest quartile of occupational respiratory PAH exposures from petroleum (OR=1.74; 95% CI=1.11-2.72) or from any source (OR=1.85; 95% CI=1.19-2.89). The gene-environment risk estimate in the highest PAH petroleum exposure quartile was greatest in men under age 60 (OR=4.52; 95% CI=1.96-10.41) or with a positive family history of prostate cancer (OR=3.02; 95% CI=1.15-7.92).
Our results suggest men who carry the GSTP1 Val(105) variant and are exposed at high levels to occupational PAH have increased risk for prostate cancer. This increased risk is more pronounced in men under age 60 or with a family history of prostate cancer.
谷胱甘肽S-转移酶(GSTP1)基因变异和职业性多环芳烃(PAH)暴露被认为是前列腺癌的风险因素。GSTP1第105位密码子的异亮氨酸/缬氨酸多态性影响其对PAH解毒的酶活性,这可能是前列腺癌发生的一种机制。
为了确定GSTP1 Ile105Val多态性是否会改变与职业性PAH暴露相关的前列腺癌风险,我们研究了来自密歇根州底特律亨利福特健康系统的637例前列腺癌病例以及244名白人和非裔美国人对照。通过对工作经历的专家审查,回顾性评估通过呼吸道和皮肤途径从木材、石油、煤炭或其他来源职业性接触PAH的情况。在调整潜在混杂因素的多重逻辑回归模型中,测试职业性PAH暴露和GSTP1 Ile105Val多态性与前列腺癌的关联。与对照相比,病例进行了过度抽样,以使用统计效率高的仅病例分析方法评估基因-环境相互作用。
GSTP1 Val(105)变异等位基因的携带情况和职业性PAH暴露均与前列腺癌无显著关联。然而,仅病例分析显示,GSTP1 Val(105)变异等位基因的携带与来自任何来源以及来自石油的职业性呼吸道PAH暴露水平升高有关(两者趋势检验p=0.01)。在职业性呼吸道PAH暴露处于最高四分位数的病例中,GSTP1 Val(105)等位基因最常被观察到,这些暴露来自石油(OR=1.74;95%CI=1.11-2.72)或任何来源(OR=1.85;95%CI=1.19-2.89)。在PAH石油暴露最高四分位数中,基因-环境风险估计在60岁以下男性(OR=4.52;95%CI=1.96-10.41)或有前列腺癌家族史的男性中最大(OR=3.02;95%CI=1.15-7.92)。
我们的结果表明,携带GSTP1 Val(105)变异且职业性PAH暴露水平高的男性患前列腺癌的风险增加。这种增加的风险在60岁以下男性或有前列腺癌家族史的男性中更为明显。