Association of Matrix Metalloproteinase-2 Genotypes With Prostate Cancer Risk

被引:8
|
作者
LI, Po-han [1 ,2 ]
Liao, Cheng-hsi [1 ,3 ,4 ]
Huang, Wen-chin [1 ,5 ]
Chang, Wen-shin [5 ]
Wu, Hsi-chin [5 ]
Hsu, Shih-wei [1 ,4 ]
Chen, Kai-yuan [6 ]
Wang, Zhi-hong [7 ]
Hsia, Te-chun [5 ]
Bau, Da-tian [1 ,4 ,5 ,8 ]
Tsai, Chia-wen [1 ,4 ,5 ]
机构
[1] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[2] China Med Univ Hosp, Dept Anesthesiol, Taichung, Taiwan
[3] Taichung Armed Forces Gen Hosp, Dept Surg, Div Urol, Taichung, Taiwan
[4] Natl Def Med Ctr, Taipei, Taiwan
[5] China Med Univ Hosp, Dept Med Res, Terry Fox Canc Res Lab, 2 Yuh Der Rd, Taichung 404, Taiwan
[6] Taichung Vet Gen Hosp, Neurol Inst, Dept Neurosurg, Taichung, Taiwan
[7] Asia Univ, Dept Food Nutr & Hlth Biotechnol, Taichung, Taiwan
[8] Asia Univ, Dept Bioinformat & Med Engn, Taichung, Taiwan
关键词
Genotype; MMP-2; polymorphism; prostate cancer; GENE POLYMORPHISMS; GASTRIC-CANCER; MMP-2; METASTASIS; SUSCEPTIBILITY; ACTIVATION; EXPRESSION; MORTALITY; METAANALYSIS; INHIBITORS;
D O I
10.21873/anticanres.16169
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Prostate cancer is one of the most commonly diagnosed malignancies among males, especially in Western populations. Matrix metalloproteinase-2 (MMP-2) plays a critical role in extracellular regulation and metastasis. However, its genotypes have seldom been examined among patients with prostate cancer (PCa). Therefore, the purpose of the study was to evaluate the association of genotypes at MMP-2 promoter-1306 (rs243865) and-735 (rs2285053) with PCa risk in a Taiwanese cohort. Materials and Methods: The profiles of MMP-2 rs243865 and rs2285053 genotypes were examined among 218 PCa patients and 436 healthy controls by polymerase chain reaction-restriction fragment length polymorphism methodologies. Results: The percentages of wild -type CC, and variant CT and TT genotypes on MMP-2 rs243865 were 88.5, 10.6, and 0.9% in the PCa case group and 85.6, 13.5, and 0.9% in the control group, respectively (p for trend=0.5544). The allelic frequency distribution showed that the variant T allele at MMP-2 rs24386 5 was not associated with PCa risk (p=0.3250). As for MMP-2 rs2285053, the results were also non-significant. In addition, there was no association between the genotypes of MMP-2 rs243865 or rs2285053 with age or smoking status on PCa risk. Conclusion: rs11568818 and rs11568819 at MMP-2 promoter region played minor roles in determining individual PCa risk.
引用
收藏
页码:343 / 349
页数:7
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