The Association Between Polymorphisms in Prooxidant or Antioxidant Enzymes (Myeloperoxidase, SOD2, and CAT) and Genes and Prostate Cancer Risk in the Chinese Population of Han Nationality

被引:16
作者
Ding, Guanxiong [1 ]
Liu, Fang [1 ,2 ]
Shen, Baixin [3 ]
Feng, Chenchen [1 ]
Xu, Jianfeng [1 ,2 ,4 ,5 ]
Ding, Qiang [1 ]
机构
[1] Fudan Univ, Dept Urol, Huashan Hosp, Shanghai 200000, Peoples R China
[2] Fudan Univ, Fudan Inst Urol, Huashan Hosp, Shanghai 200000, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 2, Dept Urol, Nanjing, Jiangsu, Peoples R China
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Urol, Winston Salem, NC 27103 USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Ctr Canc Genom, Winston Salem, NC 27103 USA
关键词
Catalase (CAT); Myeloperoxidase (MPO); Polymorphism; Prostate cancer; Superoxide dismutase (SOD2); MANGANESE SUPEROXIDE-DISMUTASE; ACTIVATOR PROTEIN-1; HYDROGEN-PEROXIDE; OXIDATIVE STRESS; DNA-DAMAGE; OVEREXPRESSION; EXPRESSION; GROWTH; CELLS; AGE;
D O I
10.1016/j.clgc.2012.08.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our study aimed to evaluate the association between the genetic polymorphisms of myeloperoxidase (MPO), superoxide dismutase (SOD2), and Catalase (CAT) and the risk of prostate cancer (PCa). Genotyping was performed by polymerase chain reaction in 1388 patients with PCa and 1008 cancer-free controls. One single-nucleotide polymorphism (SNP) of SOD2 was significantly different. Our data showed that rs5746136 was associated with a susceptibility to PCa in the Chinese population of Han nationality. Background: Oxidative stress was associated with prostate cancer (PCa). The expressions of prooxidant or antioxidant enzymes (myeloperoxidase [MPO], superoxide dismutase (SOD2), and catalase (CAT)) have been proved to be related to gene polymorphisms. Our study aimed to evaluate the association between genetic polymorphisms and the risk of PCa. Methods: Genotyping was carried out by genotyping system (MassARRAY iPLEX; Sequenom Inc, San Diego, CA) in 1388 patients with PCa and 1008 cancer-free controls in the Chinese population. Results: One SNP of SOD2 (rs5746136; P < .050, odds ratios (OR), 0.8806) was significant. Another SNP was shown to have limited association with the risk of PCa (rs554518; P = .09443) in all SNPs of CAT. In other SNPs, no significant difference was shown between genotype distributions in the patients with PCa and the control group. Conclusions: Our data showed that rs5746136 of SOD2 was associated with susceptibility to PCa in the Chinese population of Han nationality. The possible association between rs8082134 of CAT and PCa risk needs further verification.
引用
收藏
页码:251 / 255
页数:5
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