Cui Xin, Yan Hao, Ou Tong-Wen, Jia Chun-Song, Wang Qi, Xu Jian-Jun
Department of Urology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China.
Biomed Res Int. 2015;2015:674039. doi: 10.1155/2015/674039. Epub 2015 Dec 14.
Prostate cancer is a common cancer in men. Genetic variations in inflammatory response genes can potentially influence the risk of prostate cancer. We aimed to examine the association between PPARG Pro12Ala, NFKB1 -94 ins/del, NFKBIA -826C/T, COX-1 (50C>T), and COX-2 (-1195G>A) polymorphisms on prostate cancer risk. The genotypes of the polymorphisms were ascertained in 543 prostate cancer patients and 753 controls through PCR-RFLP and the risk association was evaluated statistically using logistic regression analysis. The NFKB1 -94 polymorphism was shown to decrease prostate cancer risk in both heterozygous and homozygous comparison models (odds ratios of 0.74 (95% CI = 0.58-0.96) (P = 0.02) and 0.57 (95% CI = 0.42-0.78) (P < 0.01), resp.). An opposite finding was observed for COX-2 (-1195) polymorphism (odds ratios of 1.58 (95% CI = 1.15-2.18) (P < 0.01) for heterozygous comparison model and 2.08 (95% CI = 1.48-2.92) (P < 0.01) for homozygous comparison model). No association was observed for other polymorphisms. In conclusion, NFKB1 -94 ins/del and COX-2 (-1195G>A) polymorphisms may be, respectively, associated with decreased and increased prostate cancer risk in the Chinese population.
前列腺癌是男性常见的癌症。炎症反应基因的遗传变异可能会影响前列腺癌的风险。我们旨在研究PPARG Pro12Ala、NFKB1 -94插入/缺失、NFKBIA -826C/T、COX-1(50C>T)和COX-2(-1195G>A)多态性与前列腺癌风险之间的关联。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定了543例前列腺癌患者和753例对照的多态性基因型,并使用逻辑回归分析对风险关联进行了统计学评估。在杂合子和纯合子比较模型中,NFKB1 -94多态性均显示可降低前列腺癌风险(优势比分别为0.74(95%置信区间=0.58-0.96)(P=0.02)和0.57(95%置信区间=0.42-0.78)(P<0.01))。对于COX-2(-1195)多态性,观察到相反的结果(杂合子比较模型的优势比为1.58(95%置信区间=1.15-2.18)(P<0.01),纯合子比较模型的优势比为2.08(95%置信区间=1.48-2.92)(P<0.01))。未观察到其他多态性与前列腺癌的关联。总之,在中国人群中,NFKB1 -94插入/缺失和COX-2(-1195G>A)多态性可能分别与前列腺癌风险的降低和升高有关。