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dc.contributor.authorRibeiro, Betania Fachetti-
dc.contributor.authorIglesias, Déborah Pitta Paraíso-
dc.contributor.authorNascimento, G. J. F.-
dc.contributor.authorGalvão, Hebel Cavalcanti-
dc.contributor.authorMedeiros, Ana Miryam Costa de-
dc.contributor.authorFreitas, Roseana de Almeida-
dc.identifier.citationRIBEIRO, B. F. et al. Immunoexpression of MMPs-1, -2, and -9 in ameloblastoma and odontogenic adenomatoid tumor. Oral Diseases, v. 15, n. 7, p. 472-477, 2009.pt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectOdontogenic adenomatoid tumorpt_BR
dc.subjectMatrix metalloproteinasespt_BR
dc.subjectExtracellular matrixpt_BR
dc.titleImmunoexpression of MMPs-1, -2, and -9 in ameloblastoma and odontogenic adenomatoid tumorpt_BR
dc.description.resumoOBJECTIVE: The aim of this study was to evaluate and compare the expression of metalloproteinases-1, -2, and -9 in solid ameloblastoma and adenomatoid odontogenic tumor. METHODS: A total of 20 cases of solid ameloblastoma and 10 cases of adenomatoid odontogenic tumors were selected and immunohistochemically assessed. Metalloproteinases-1, -2, and -9 immunoexpression and their distribution pattern were noted and semiquantitatively scored. The scores obtained were statistically analyzed. RESULTS: Matrix metalloproteinase (MMP)-1 showed a predominant expression in both tumors and was found in stroma and parenchyma. For MMP-2, there was a varied expression, with 80% and 60% of immunoreactive tumor cells in ameloblastoma and adenomatoid odontogenic tumor respectively. Regarding stromal cells, 65% of ameloblastomas and 80% of adenomatoid odontogenic tumors showed positivity. There was immunoexpression of the MMP-9 in parenchymal and stromal cells in all cases of both tumors analyzed. A statistically significant difference in the expression of MMP-1 in relation to the expression of MMP-2 and -9 in ameloblastomas (P < 0.001) was observed. CONCLUSION: The results suggest that these metalloproteinases are related to growth and progression of tumors analyzed, and particularly in ameloblastoma, its highest aggressiveness may be, in part, a result of the active participation of the stromal cells and their products, such as the MMPs studied.pt_BR
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