Association between endothelial nitric oxide synthase 894G>T polymorphism and prostate cancer risk: a meta-analysis of literature studies

被引:9
作者
Zhao, Cheng [1 ,3 ]
Yan, Weiqian [2 ]
Zu, Xiongbing [1 ]
Chen, Minfeng [1 ]
Liu, Longfei [1 ]
Zhao, Shushan [3 ]
Liu, Hong [3 ]
Hu, Xia [3 ]
Luo, Renna [3 ]
Xia, Yang [3 ]
Qi, Lin [1 ]
机构
[1] Cent S Univ, Xiangya Hosp, Dept Urol, Changsha 410008, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
[3] Univ Texas Hlth Sci Ctr Houston, Dept Biochem & Mol Biol, Houston, TX 77030 USA
关键词
Endothelial nitric oxide synthase; NOS3; eNOS; Polymorphism; Prostate cancer; Meta-analysis; GENE POLYMORPHISMS; GLU298ASP POLYMORPHISM; SUSCEPTIBILITY; METASTASIS; SUPPRESSES; BLOOD;
D O I
10.1007/s13277-014-2097-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To date, several studies have been conducted to assess the association between endothelial nitric oxide synthase (eNOS) gene 894G>T polymorphismand prostate cancer (PCa) risk, but the results are conflicting. To derive a more precise estimation of the relationship between 894G>T polymorphism and PCa risk, the present meta-analysis was performed. A total of eight case-control studies were included in this meta-analysis. The pooled odds ratio (OR) with 95% confidence interval (CI) was calculated to evaluate the associations. Our results suggested that 894G>T polymorphism is associated with PCa risk under codominant (GT vs. GG) (OR=1.11, 95 % CI=1.01-1.22, P=0.04) and overdominant (GT vs. GG+ TT) (OR=1.12, 95 % CI=1.02-1.23, P=0.02) models in the overall population, while there are no associations observed under dominant (GT+TT vs. GG), recessive (TT vs. GG+ GT), and allelic (T vs. G) models. Moreover, when the eligible studies were stratified according to sources of control, significant association between 894G>T polymorphism and susceptibility of PCa was also identified under codominant (OR=1.12, 95 % CI=1.01-1.24, P=0.03) and overdominant (OR=1.13, 95 % CI=1.02-1.25, P=0.02) models when using healthy individuals as control. However, there are no significant associations found under any genetic models when using BPH patients as control group. In conclusion, the present meta-analysis suggested that the eNOS gene 894G>T polymorphism might be a risk factor in the onset of PCa.
引用
收藏
页码:11727 / 11733
页数:7
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