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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130990
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dc.contributor.authorAfonso, M.-
dc.contributor.authorPerrotti, V.-
dc.contributor.authorRapani, M.-
dc.contributor.authorIaculli, F.-
dc.contributor.authorPiccirilli, M.-
dc.contributor.authorOnuma, T.-
dc.contributor.authorShibli, J. A.-
dc.contributor.authorOliveira Bello, V. de-
dc.contributor.authorSposto, M. R.-
dc.contributor.authorArtese, L.-
dc.date.accessioned2015-12-07T15:30:39Z-
dc.date.accessioned2016-10-25T21:22:28Z-
dc.date.available2015-12-07T15:30:39Z-
dc.date.available2016-10-25T21:22:28Z-
dc.date.issued2014-
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/24632797-
dc.identifier.citationMinerva Stomatologica, v. 63, n. 3, p. 59-67, 2014.-
dc.identifier.issn0026-4970-
dc.identifier.urihttp://hdl.handle.net/11449/130990-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130990-
dc.description.abstractIn the present immunohistochemical study, the expression of vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67 in the gingival tissues of renal transplant patients treated with cyclosporin A was assessed. Gingival overgrowth (GO) frequently occurs in transplant patients receiving immunosuppressive drugs such as cyclosporine and this gingival inflammation might play an important role in the pathogenesis of drug-induced GO. Twenty-eight human gingival biopsies were taken from healthy patients with chronic periodontitis (N.=14 control group), and from renal transplant recipients treated with cyclosporin A (N.=14 test group). The retrieved specimens were immunohistochemically processed and stained for vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67. The levels of vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67 were found to be significantly different among groups (P>0.001), with patients treated with cyclosporin A showing higher levels of all the analyzed markers compared to control group. In summary, the data from this pilot study suggests that the investigated factors have a role in the inflammation processes associated to immunosuppressive therapy. However, further studies with a larger sample population need to be conducted for an exhaustive knowledge of the mechanisms leading to GO.en
dc.format.extent59-67-
dc.language.isoeng-
dc.publisherMinerva Medica-
dc.sourcePubMed-
dc.titleImmunoexpression of angiogenesis and proliferation markers in patients treated with cyclosporin Aen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversity of Chieti‑Pescara Chieti-
dc.contributor.institutionUniversidade de Guarulhos (UNG)-
dc.description.affiliationDepartment of Diagnosis and Oral Surgery Araraquara Dental School, UNESP Araraquara, SP, Brazil-
dc.description.affiliationDepartment of Medical, Oral and Biotechnological Sciences Dental School, University of Chieti‑Pescara Chieti, Italy-
dc.description.affiliationDepartment of Periodontology Dental Research Division, Guarulhos University Guarulhos, SP, Brazil-
dc.description.affiliationKidney Transplant Unit Base Hospital, Brasilia, Brazil.-
dc.description.affiliationUnespDepartment of Diagnosis and Oral Surgery Araraquara Dental School, UNESP Araraquara, SP, Brazil - v.perrotti@unich.it.-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMinerva Stomatologica-
dc.identifier.pubmed24632797-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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