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http://repositorio.ufc.br/handle/riufc/21487
Tipo: | Artigo de Periódico |
Título: | Evaluation of the p-AKT, p-JNK and FoxO3a function in the oral epithelial dysplasia malignance |
Autor(es): | Chaves, Filipe Nobre Marinho, Thâmara Manoela Bezerra Silva, Paulo Goberlânio de Barros Oliveira, Francisco Artur Forte Sousa, Fabrício Bitu Costa, Fábio Wildson Gurgel Alves, Ana Paula Negreiros Nunes Pereira, Karuza Maria Alves |
Palavras-chave: | Carcinoma;Citoplasma;Cytoplasm |
Data do documento: | 2016 |
Instituição/Editor/Publicador: | Oral Diseases |
Citação: | CHAVES, 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. |
Abstract: | OBJECTIVES: 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. |
URI: | http://www.repositorio.ufc.br/handle/riufc/21487 |
ISSN: | 1354-523X |
Aparece nas coleções: | DCOD - Artigos publicados em revistas científicas |
Arquivos associados a este item:
Arquivo | Descrição | Tamanho | Formato | |
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2016_art_fnchaves.pdf | 1,32 MB | Adobe PDF | Visualizar/Abrir |
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