dc.creatorREIS, Sabrina Thalita dos
dc.creatorPONTES JR., Jose
dc.creatorVILLANOVA, Fabiola Elizabeth
dc.creatorBORRA, Priscila Maria de Andrade
dc.creatorANTUNES, Alberto Azoubel
dc.creatorDALL`OGLIO, Marcos Francisco
dc.creatorSrougi, Miguel
dc.creatorLEITE, Katia Ramos Moreira
dc.date.accessioned2012-10-19T18:25:37Z
dc.date.accessioned2018-07-04T15:12:37Z
dc.date.available2012-10-19T18:25:37Z
dc.date.available2018-07-04T15:12:37Z
dc.date.created2012-10-19T18:25:37Z
dc.date.issued2009
dc.identifierJOURNAL OF UROLOGY, v.181, n.5, p.2320-2325, 2009
dc.identifier0022-5347
dc.identifierhttp://producao.usp.br/handle/BDPI/23316
dc.identifier10.1016/j.juro.2009.01.012
dc.identifierhttp://dx.doi.org/10.1016/j.juro.2009.01.012
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1620046
dc.description.abstractPurpose: Prostate cancer is the most common tumor in males in Brazil. Single nucleotide polymorphisms have been demonstrated to exist in the promoter regions of matrix metalloproteinase genes and they are associated with the development and progression of some cancers. We investigated the correlation between MMP1, 2, 7 and 9 polymorphisms with susceptibility to prostate cancer, and classic prognostic parameters of prostate cancer. Materials and Methods: Genomic DNA was extracted using conventional protocols. The DNA sequence containing the polymorphic site was amplified by realtime polymerase chain reaction using TaqMan (R) fluorescent probes. Results: For the MMP1 gene the polymorphic allele was more common in the control group than in the prostate cancer group (p <0.001). For the MMP9 gene the incidence of the polymorphic homozygote genotype was higher in the prostate cancer group (p <0.001). For higher stage tumors (pT3) a polymorphic allele in the MMP2 gene was more common (p = 0.026). When considering Gleason score, the polymorphic homozygote genotype of MMP9 was more common in Gleason 6 or less tumors (p = 0.003), while a polymorphic allele in the MMP2 gene was more common in Gleason 7 or greater tumors (p = 0.042). Conclusions: MMP1 and MMP2 may protect against prostate cancer development and MMP9 may be related to higher risk. In contrast, MMP9 polymorphism was associated with a lower Gleason score and MMP2 polymorphism was associated with nonorgan confined disease.
dc.languageeng
dc.publisherELSEVIER SCIENCE INC
dc.relationJournal of Urology
dc.rightsCopyright ELSEVIER SCIENCE INC
dc.rightsrestrictedAccess
dc.subjectprostate
dc.subjectprostatic neoplasms
dc.subjectpolymorphisms, genetic
dc.subjectmatrix metalloproteinases
dc.subjectgene expression
dc.titleGenetic Polymorphisms of Matrix Metalloproteinases: Susceptibility and Prognostic Implications for Prostate Cancer
dc.typeArtículos de revistas


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