Please use this identifier to cite or link to this item: http://www.repositorio.ufc.br/handle/riufc/21487
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dc.contributor.authorChaves, Filipe Nobre-
dc.contributor.authorMarinho, Thâmara Manoela Bezerra-
dc.contributor.authorSilva, Paulo Goberlânio de Barros-
dc.contributor.authorOliveira, Francisco Artur Forte-
dc.contributor.authorSousa, Fabrício Bitu-
dc.contributor.authorCosta, Fábio Wildson Gurgel-
dc.contributor.authorAlves, Ana Paula Negreiros Nunes-
dc.contributor.authorPereira, Karuza Maria Alves-
dc.date.accessioned2017-01-10T16:09:13Z-
dc.date.available2017-01-10T16:09:13Z-
dc.date.issued2016-
dc.identifier.citationCHAVES, F. N. et al. Evaluation of the p-AKT, p-JNK and FoxO3a function in the oral epithelial dysplasia malignance. Oral Diseases, Houndmills, p. 1-27, 2016.pt_BR
dc.identifier.issn1354-523X-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/21487-
dc.description.abstractOBJECTIVES: To evaluate the expression of p-AKT, p-JNK, FoxO3a and KI-67 in samples of Oral Squamous Cell Carcinoma (OSCC) and Oral Epithelial Dysplasias (OEDs) to understand their possible involvement in the malignant transformation process of oral lesions. MATERIALS AND METHODS: Tissue samples of 20 cases of OSCCs, 20 OEDs and normal oral mucosa were subjected to immunohistochemistry reactions for anti-p-Akt, anti-p-JNK, anti-FoxO3a and anti-Ki-67 antibodies. It was analyzed quantitative (number of immunostained cells) and qualitative (immunostaining intensity) parameters in different cell immunostaining sublocations. RESULTS: Nuclear p-AKT was observed significantly greater immunostaining in OSCC (21.2 ± 19.0) than in dysplasias (7.9 ± 8.1) and control (1.8 ± 4.7) (p = 0.002). Immunostaining of strong nuclear p-JNK was greater in controls (48.3 ± 13.7) than in OEDs (11.0 ± 10.3) and OSCCs (1.1 ± 1.3) (p<0.001). Strong nuclear immunostaining of FoxO3a proved to be absent in OSCCs (0.0 ± 0.1) with little staining on dysplasias (3.2 ± 5.4) and increased expression in controls (13.5 ± 4.8) (p<0.001). Immunostaining of strong nuclear ki-67 was grater in OSCCs (48.1±49.6) than in OED (11.8±10.6) and controls (1.9±2.0) (p<0.001). CONCLUSIONS: Malignant process of OEDs in this research may involve the same mechanisms of established malignant lesions.pt_BR
dc.language.isoenpt_BR
dc.publisherOral Diseasespt_BR
dc.subjectCarcinomapt_BR
dc.subjectCitoplasmapt_BR
dc.subjectCytoplasmpt_BR
dc.titleEvaluation of the p-AKT, p-JNK and FoxO3a function in the oral epithelial dysplasia malignancept_BR
dc.typeArtigo de Periódicopt_BR
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