School of Public Health, College of Public Health and Nutrition, Taipei Medical University, Taipei 110, Taiwan.
Department of Urology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Biomed Res Int. 2018 May 21;2018:3148137. doi: 10.1155/2018/3148137. eCollection 2018.
Cigarette smoking and exposure to environmental tobacco smoke are well-known risk factors for urothelial carcinoma (UC). We conducted a hospital-based case-control study involving 287 UC cases and 574 cancer-free controls to investigate the joint effects of cigarette smoking and polymorphisms of inflammatory genes on UC risk. Tumor necrosis factor alpha (TNF-) 308 G/A and interleukin-8 (IL-8) -251 T/A polymorphisms were determined using a polymerase chain reaction-restriction fragment length polymorphism method. People who had ever smoked and those who were exposed to environmental tobacco smoke had significantly increased UC odds ratios (ORs) of 1.65 and 1.68, respectively. Participants who had smoked more than 18 pack-years had a significantly increased UC OR of 2.64. People who had ever smoked and who carried the A/A genotype of the 308 G/A polymorphism had a significantly higher UC OR (10.25) compared to people who had never smoked and who carried the G/G or G/A genotype. In addition, people who had ever smoked and who carried the -251 T/T genotype had a significantly increased UC OR (3.08) compared to people who had never smoked and who carried the T/A or A/A genotype. In a combined analysis of three major risk factors (cumulative cigarette smoking, the 308 A/A genotype, and the -251 T/T genotype), subjects with any one, any two, and all three risk factors experienced significantly increased UC ORs of 1.55, 2.89, and 3.77, respectively, compared to individuals with none of the risk factors. . Our results indicate that the combined effects of cumulative cigarette exposure and the 308 A/A genotype and/or the -251 T/T genotype on UC OR showed a significant dose-response relationship.
吸烟和暴露于环境烟草烟雾是已知的膀胱癌(UC)危险因素。我们进行了一项基于医院的病例对照研究,共纳入 287 例膀胱癌病例和 574 例无癌症对照,以探讨吸烟和炎症基因多态性对 UC 风险的联合作用。采用聚合酶链反应-限制性片段长度多态性方法检测肿瘤坏死因子-α(TNF-α)308 G/A 和白细胞介素-8(IL-8)-251 T/A 多态性。曾经吸烟和暴露于环境烟草烟雾的人 UC 比值比(OR)分别显著增加 1.65 和 1.68。曾经吸烟且吸烟量超过 18 包/年的人 UC OR 显著增加 2.64。曾经吸烟且携带 308 G/A 多态性 A/A 基因型的人 UC OR 显著升高(10.25),与从未吸烟且携带 G/G 或 G/A 基因型的人相比。此外,曾经吸烟且携带 -251 T/T 基因型的人 UC OR 显著升高(3.08),与从未吸烟且携带 T/A 或 A/A 基因型的人相比。在对三个主要危险因素(累积吸烟、308 A/A 基因型和-251 T/T 基因型)的综合分析中,与无任何危险因素的个体相比,任何一种、两种或三种危险因素的个体的 UC OR 分别显著升高 1.55、2.89 和 3.77。我们的研究结果表明,累积吸烟暴露与 308 A/A 基因型和/或-251 T/T 基因型对 UC OR 的联合作用呈显著剂量反应关系。