dc.contributorPinto, Leão Pereira
dc.contributorhttp://lattes.cnpq.br/4634092517001105
dc.contributorhttp://lattes.cnpq.br/7040457616034306
dc.contributorSouza, Lelia Batista de
dc.contributorhttp://lattes.cnpq.br/6671914892609743
dc.contributorCavalcante, Roberta Barroso
dc.contributorhttp://lattes.cnpq.br/6510605059677599
dc.creatorBarros, Joyce Magalhães de
dc.date.accessioned2021-09-15T15:32:56Z
dc.date.accessioned2022-10-05T22:59:15Z
dc.date.available2021-09-15T15:32:56Z
dc.date.available2022-10-05T22:59:15Z
dc.date.created2021-09-15T15:32:56Z
dc.date.issued2021-07-07
dc.identifierBARROS, Joyce Magalhães de. Imunoexpressão da proteína ING3 em Queilites Actínicas e carcinomas de células escamosas de lábio inferior. 2021. 89f. Dissertação (Mestrado em Ciências Odontológicas) - Centro de Ciências da Saúde, Universidade Federal do Rio Grande do Norte, Natal, 2021.
dc.identifierhttps://repositorio.ufrn.br/handle/123456789/33666
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3943744
dc.description.abstractThe family of inhibitors of growth (ING) corresponds to a group of tumor suppressor genes whose expression is altered or absent in several types of cancer. The products of these genes are mainly related to cellular processes indispensable in carcinogenesis, including cell proliferation, DNA replication and repair. This study evaluated the immunohistochemical expression of ING3 protein in 45 actinic cheilitis (AC) and 48 lower lip squamous cell carcinoma (CCELI) specimens. Protein expression was compared between the two groups of samples, as well as with the clinicopathological parameters of studied lesions, using Fisher's exact tests, Kruskal-Wallis (KW), Mann-Whitney (U) and correlation test of Spearman. A significance level of 5% was adopted for all tests, with values of p ≤ 0.05 being considered significant. No statistically significant associations were found between morphological variables of CCELI and tumor size, lymph node involvement, clinical staging, local recurrence and lymph node metastasis after treatment (p>0.05). Deaths were significantly more frequent in tumors with a high histopathological risk score (p<0.05). In ACs, significant differences in nuclear-cytoplasmic and restricted to the cytoplasm expression of ING3, with gradation of Kujan et al. (2006) were found (p<0.05). In CCELIs, there was no statistically significant difference when comparing ING3 expressions (nucleocytoplasmic and cytoplasmic restricted) with clinical and morphological parameters (p>0.05). Nucleocytoplasmic ING3 expression was significantly lower in CCELI when compared to AC cases (p<0.05) and cytoplasm-restricted expression was significantly higher in CCELIs (p<0.05). Our results suggest that there is a remarkable decrease in ING3 nuclear expression according to malignant progression, indicating an impaired tumor suppressor function of this protein in AC and CCELI. However, it is believed that, in lip carcinogenesis, ING3 is better characterized as predictive marker of malignant transformation, rather than a biomarker of tumor biological behavior.
dc.publisherUniversidade Federal do Rio Grande do Norte
dc.publisherBrasil
dc.publisherUFRN
dc.publisherPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS ODONTOLÓGICAS
dc.rightsAcesso Aberto
dc.subjectCarcinoma de células escamosas
dc.subjectCarcinogênese
dc.subjectQueilite
dc.subjectBiomarcadores tumorais
dc.titleImunoexpressão da proteína ING3 em Queilites Actínicas e carcinomas de células escamosas de lábio inferior
dc.typemasterThesis


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