Matrix metalloproteinase-2 polymorphism is associated with prognosis in prostate cancer

被引:15
|
作者
dos Reis, Sabrina Thalita [1 ]
Villanova, Fabiola Elizabeth [1 ]
Andrade, Priscila Maria [1 ]
Pontes, Jose, Jr. [1 ]
de Sousa-Canavez, Juliana Moreira [2 ]
Sanudo, Adriana [1 ]
Antunes, Alberto Azoubel [1 ]
Dall'Oglio, Marcos Francisco [1 ]
Srougi, Miguel [1 ]
Moreira Leite, Katia Ramos [1 ]
机构
[1] Univ Sao Paulo, Lab Med Invest LIM55, Dept Urol, Fac Med, Sao Paulo, Brazil
[2] Genoa Biotechnol, Sao Paulo, Brazil
关键词
Disease susceptibility; Metalloproteinases; Polymorphism; Prognosis; Prostate cancer; SINGLE NUCLEOTIDE POLYMORPHISM; GENETIC POLYMORPHISMS; TISSUE INHIBITOR; PROMOTER; RISK; MATRIX-METALLOPROTEINASE-2; IDENTIFICATION; METASTASIS; STATISTICS; EXPRESSION;
D O I
10.1016/j.urolonc.2008.10.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Prostate cancer (PCa) is the most frequent tumor in males in Brazil. Single nucleotide polymorphisms (SNP) have been demonstrated in the promoter region of matrix metalloproteinases (MMPs) genes and have been associated with development and progression of some cancers. In this study, our aim was to investigate a possible relation between polymorphism of the promoter region of the MMP2 gene and classical prognostic parameters in prostate cancer. Materials and methods: Genomic DNA was extracted using conventional protocols. The DNA sequence containing the polymorphic site was amplified by real-time polymerase chain reaction, using fluorescent probes (TaqMan). Results: In patients with tumors of a higher stage (pT3), a polymorphic allele in the MMP2 gene was more frequent (P = 0.026) than in patients with lower tumor stage. A polymorphic allele in the MMP2 gene was more frequent in Gleason >= 7 than in Gleason <= 6 (P = 0.042). Conclusions: We conclude that MMP2 polymorphism can be used together with pathological stage and Gleason score to identify patients with worse prognosis. Our results illustrate the potential use of MMP2 SNP as a molecular marker for prostate cancer. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:624 / 627
页数:4
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