Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais

Detalhes bibliográficos
Autor(a) principal: Almeida, Dennys Ramon de Melo Fernandes
Data de Publicação: 2014
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/15428
Resumo: P16 is a tumor suppressor gene widely studied in lesions associated with human papillomavirus (HPV) since its overexpression is caused by viral protein E7. Furthermore, this molecule can interact with cyclin D1, an important regulator of cell cycle used a marker of tumor aggressiveness. The expression of the human Ki-67 protein is strictly associated with cell proliferation and consequently the degree of malignancy and prognosis of tumors. This study aimed to evaluate the immunohistochemical expression of p16, cyclin D1 and Ki67 in benign oral lesions showing Koilocytosis and squamous cell carcinoma (CEC) with or without microscopic evidence of viral infection. This is a retrospective study, quantitative and cross carried by lifting paraffin blocks performed in Oral Pathology Laboratory of the course of the Federal University of Ceará Dentistry, from 2008 to 2013. We selected 89 samples grouped in 25 fibroepithelial hyperplasia with Koilocytosis (HFE / Col); 16 oral squamous papillomas (PO); 28 oral squamous cell carcinomas (CEC), subdivided among patients younger than 50 years (CEC-50) and above 50 years (CEC + 50). Were used in 20 cases of fibroepithelial hyperplasia (HFE) as a negative control. In histological review of all groups, except for CEC + 50, cytological changes were found consistent with Koilocytosis (p <0.001). Females were the most prevalent in the whole sample is not, however, statistically significant (p = 0.830). The most affected age groups, in all groups, were the fourth and fifth decades of life, however, without statistical significance (p = 0701). The most common anatomical location in the HFE / Col was the alveolar ridge followed by buccal mucosa in the mouth floor PO and alveolar ridge, the CEC under age 50 the tongue and palate and in cases of CEC over 50 years the tongue, this last significantly (p = 0.015). All benign oral lesions and the group of CEC-50 showed high immunostaining for p16 and cyclin D1, which was statistically significant compared to the negative control (HFE) (p <0.001). The quantitative expression of Ki67 was significantly higher in CEC-50 in the control group (HFE) (p <0.001). We conclude that oral lesions with Koilocytosis (papilloma, HFE / Col and CEC-50) are positive for p16 and cyclin D1 suggests a possible association of pathogenesis with human papillomavirus.
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spelling Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões oraisImmunohistochemical P16 expression, cyclin D1 and KI67 in oral injuriesNeoplasias BucaisCiclina D1P16 is a tumor suppressor gene widely studied in lesions associated with human papillomavirus (HPV) since its overexpression is caused by viral protein E7. Furthermore, this molecule can interact with cyclin D1, an important regulator of cell cycle used a marker of tumor aggressiveness. The expression of the human Ki-67 protein is strictly associated with cell proliferation and consequently the degree of malignancy and prognosis of tumors. This study aimed to evaluate the immunohistochemical expression of p16, cyclin D1 and Ki67 in benign oral lesions showing Koilocytosis and squamous cell carcinoma (CEC) with or without microscopic evidence of viral infection. This is a retrospective study, quantitative and cross carried by lifting paraffin blocks performed in Oral Pathology Laboratory of the course of the Federal University of Ceará Dentistry, from 2008 to 2013. We selected 89 samples grouped in 25 fibroepithelial hyperplasia with Koilocytosis (HFE / Col); 16 oral squamous papillomas (PO); 28 oral squamous cell carcinomas (CEC), subdivided among patients younger than 50 years (CEC-50) and above 50 years (CEC + 50). Were used in 20 cases of fibroepithelial hyperplasia (HFE) as a negative control. In histological review of all groups, except for CEC + 50, cytological changes were found consistent with Koilocytosis (p <0.001). Females were the most prevalent in the whole sample is not, however, statistically significant (p = 0.830). The most affected age groups, in all groups, were the fourth and fifth decades of life, however, without statistical significance (p = 0701). The most common anatomical location in the HFE / Col was the alveolar ridge followed by buccal mucosa in the mouth floor PO and alveolar ridge, the CEC under age 50 the tongue and palate and in cases of CEC over 50 years the tongue, this last significantly (p = 0.015). All benign oral lesions and the group of CEC-50 showed high immunostaining for p16 and cyclin D1, which was statistically significant compared to the negative control (HFE) (p <0.001). The quantitative expression of Ki67 was significantly higher in CEC-50 in the control group (HFE) (p <0.001). We conclude that oral lesions with Koilocytosis (papilloma, HFE / Col and CEC-50) are positive for p16 and cyclin D1 suggests a possible association of pathogenesis with human papillomavirus.O p16 é um gene supressor de tumor amplamente estudado nas lesões associadas ao Papilomavírus Humano (HPV) visto que sua superexpressão é causada pela proteína viral E7. Além disso, esta molécula pode interagir com ciclina D1, importante regulador do ciclo celular, utilizado como marcador de agressividade tumoral. A expressão da proteína humana Ki67 está estritamente relacionada com a proliferação celular e consequentemente com o grau de malignidade e prognóstico das neoplasias. O presente estudo objetivou avaliar a expressão imunoistoquímica de p16, ciclina D1 e Ki67 em lesões orais benignas exibindo coilocitose e no carcinoma de células escamosas (CEC) com ou sem evidência microscópica de infecção viral. Trata-se de um estudo retrospectivo, quantitativo e transversal realizado por meio do levantamento de blocos parafinados realizado no Laboratório de Patologia Bucal do curso de Odontologia da Universidade Federal do Ceará, no período de 2008 a 2013. Foram selecionadas 89 amostras agrupadas em: 25 hiperplasias fibroepiteliais com coilocitose (HFE/Col); 16 papilomas escamosos orais (PO); 28 carcinomas de células escamosas orais (CEC), subdividido entre pacientes abaixo de 50 anos (CEC-50) e acima de 50 anos (CEC+50). Utilizaram-se 20 casos de hiperplasias fibroepiteliais (HFE) como controle negativo. Na revisão histológica de todos os grupos, exceto no CEC+50, foram encontradas alterações citológicas consistentes com coilocitose (p<0.001). O sexo feminino foi o mais prevalente em toda a amostra não sendo, contudo, estatisticamente significante (p=0.830). As faixas etárias mais afetadas, em todos os grupos, foram a quarta e a quinta décadas de vida, no entanto, sem significância estatística (p=0.701). A localização anatômica mais frequente no HFE/Col foi o rebordo alveolar seguida da mucosa jugal, no PO o assoalho bucal e rebordo alveolar, no CEC abaixo de 50 anos a língua e palato e nos casos de CEC acima de 50 anos a língua, este último de forma significante (p=0.015). Todas as lesões orais benignas e o grupo de CEC-50 apresentaram elevada imunomarcação para p16 e ciclina D1, sendo estatisticamente significante em relação ao controle negativo (HFE) (p<0.001). A expressão quantitativa por Ki67 foi significantemente maior no CEC-50 em relação ao grupo controle (HFE) (p<0.001). Conclui-se que as lesões orais com coilocitose (papiloma, HFE/Col e CEC-50) apresentam positividade para p16 e ciclina D1 sugerindo possível associação da patogênese com o papilomavírus humano.Alves, Ana Paula Negreiros NunesAlmeida, Dennys Ramon de Melo Fernandes2016-03-09T15:46:29Z2016-03-09T15:46:29Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfALMEIDA, D. R. M. F. Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais. 2014. 68 f. Dissertação (Mestrado em Patologia) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2014.http://www.repositorio.ufc.br/handle/riufc/15428porreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2019-01-21T17:08:18Zoai:repositorio.ufc.br:riufc/15428Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2019-01-21T17:08:18Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
Immunohistochemical P16 expression, cyclin D1 and KI67 in oral injuries
title Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
spellingShingle Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
Almeida, Dennys Ramon de Melo Fernandes
Neoplasias Bucais
Ciclina D1
title_short Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
title_full Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
title_fullStr Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
title_full_unstemmed Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
title_sort Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais
author Almeida, Dennys Ramon de Melo Fernandes
author_facet Almeida, Dennys Ramon de Melo Fernandes
author_role author
dc.contributor.none.fl_str_mv Alves, Ana Paula Negreiros Nunes
dc.contributor.author.fl_str_mv Almeida, Dennys Ramon de Melo Fernandes
dc.subject.por.fl_str_mv Neoplasias Bucais
Ciclina D1
topic Neoplasias Bucais
Ciclina D1
description P16 is a tumor suppressor gene widely studied in lesions associated with human papillomavirus (HPV) since its overexpression is caused by viral protein E7. Furthermore, this molecule can interact with cyclin D1, an important regulator of cell cycle used a marker of tumor aggressiveness. The expression of the human Ki-67 protein is strictly associated with cell proliferation and consequently the degree of malignancy and prognosis of tumors. This study aimed to evaluate the immunohistochemical expression of p16, cyclin D1 and Ki67 in benign oral lesions showing Koilocytosis and squamous cell carcinoma (CEC) with or without microscopic evidence of viral infection. This is a retrospective study, quantitative and cross carried by lifting paraffin blocks performed in Oral Pathology Laboratory of the course of the Federal University of Ceará Dentistry, from 2008 to 2013. We selected 89 samples grouped in 25 fibroepithelial hyperplasia with Koilocytosis (HFE / Col); 16 oral squamous papillomas (PO); 28 oral squamous cell carcinomas (CEC), subdivided among patients younger than 50 years (CEC-50) and above 50 years (CEC + 50). Were used in 20 cases of fibroepithelial hyperplasia (HFE) as a negative control. In histological review of all groups, except for CEC + 50, cytological changes were found consistent with Koilocytosis (p <0.001). Females were the most prevalent in the whole sample is not, however, statistically significant (p = 0.830). The most affected age groups, in all groups, were the fourth and fifth decades of life, however, without statistical significance (p = 0701). The most common anatomical location in the HFE / Col was the alveolar ridge followed by buccal mucosa in the mouth floor PO and alveolar ridge, the CEC under age 50 the tongue and palate and in cases of CEC over 50 years the tongue, this last significantly (p = 0.015). All benign oral lesions and the group of CEC-50 showed high immunostaining for p16 and cyclin D1, which was statistically significant compared to the negative control (HFE) (p <0.001). The quantitative expression of Ki67 was significantly higher in CEC-50 in the control group (HFE) (p <0.001). We conclude that oral lesions with Koilocytosis (papilloma, HFE / Col and CEC-50) are positive for p16 and cyclin D1 suggests a possible association of pathogenesis with human papillomavirus.
publishDate 2014
dc.date.none.fl_str_mv 2014
2016-03-09T15:46:29Z
2016-03-09T15:46:29Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv ALMEIDA, D. R. M. F. Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais. 2014. 68 f. Dissertação (Mestrado em Patologia) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2014.
http://www.repositorio.ufc.br/handle/riufc/15428
identifier_str_mv ALMEIDA, D. R. M. F. Expressão imunoistoquímica de P16, ciclina D1 e KI67 em lesões orais. 2014. 68 f. Dissertação (Mestrado em Patologia) - Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, 2014.
url http://www.repositorio.ufc.br/handle/riufc/15428
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dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
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reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
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