Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Feitosa, Sthefane Gomes
Orientador(a): Pereira, Karuza Maria Alves
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://www.repositorio.ufc.br/handle/riufc/30029
Resumo: Odontogenic cysts are relatively common lesions that cause bone destruction in the jaws. They are classified according to their origin in: developmental cysts, including odontogenic keratocyst (OKC), or in inflammatory cysts. Odontogenic tumors correspond to a complex group of lesions of different histopathological types and clinical behaviors, being classified according to their origin. Among tumors of odontogenic epithelial origin, ameloblastoma (AM) is often significant, tumor due to its slow growth and clinical feature of local invasiveness. The pathogenesis of odontogenic cysts and tumors is still little elucidated and studies aim to identify mechanisms and pathways involved in the formation and progression of these lesions. In this context, the PI3K / AKT / PTEN pathway has been analyzed in some odontogenic cysts and tumors in order to understand mechanisms involved in these lesions. Thus, the present study aimed to analyze and compare the immunohistochemical expression of PI3K and PTEN in odontogenic keratocysts and ameloblastomas. The sample consisted of 10 OKC and 10 AM. Immunohistochemical screening was performed using the anti-PI3K (1:400) and anti-PTEN (1:400). Mean ± SEM of the calculated cell counts and histories were expressed and analyzed by the Mann-Whitney test, followed by Dunn's post-test and correlated using Spearman's correlation. The categorical data were expressed as absolute frequency and compared using Fisher's Exact or Pearson's Chi-square test. Immunohistochemical analysis showed positive immunoblot in all cases of the sample. The total nuclear-stained cells for OKC PTEN were 39.21 ± 12.38 immunopositive cells and AM were 93.60 ± 2.45 (p <0.001). The cytoplasmic immunoexpression of PTEN to OKC was 87.35 ± 5.72 cells immunolabelled and 99.30 ± 0.48 for AM (p = 0.023). The comparison between the histoscore nucleus of PTEN in the OKC (4.90 ± 1.36) and in the AM (11.20 ± 0.53) (p=0.003), also evidencing statistical significance in the comparison of histoscore cytoplasm (p=0.011). The correlation between the percentages of PI3K and PTEN immunoblotting in OKC showed a statistically significant relationship between the percentage of cytoplasmic immunoexpression (p=0.019). Considering the results obtained in this research, it can be concluded that PI3K and PTEN are present in the epithelial constituents of OKC and AM. It is suggested that the PI3K / PTEN pathway may be active in OKC because the negative correlation of PI3K and PTEN is found in this odontogenic cyst.
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spelling Feitosa, Sthefane GomesPereira, Karuza Maria Alves2018-03-02T17:37:10Z2018-03-02T17:37:10Z2018-02-15FEITOSA, S. G. Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas. 2018. 67 f. Dissertação (Mestrado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2018.http://www.repositorio.ufc.br/handle/riufc/30029Odontogenic cysts are relatively common lesions that cause bone destruction in the jaws. They are classified according to their origin in: developmental cysts, including odontogenic keratocyst (OKC), or in inflammatory cysts. Odontogenic tumors correspond to a complex group of lesions of different histopathological types and clinical behaviors, being classified according to their origin. Among tumors of odontogenic epithelial origin, ameloblastoma (AM) is often significant, tumor due to its slow growth and clinical feature of local invasiveness. The pathogenesis of odontogenic cysts and tumors is still little elucidated and studies aim to identify mechanisms and pathways involved in the formation and progression of these lesions. In this context, the PI3K / AKT / PTEN pathway has been analyzed in some odontogenic cysts and tumors in order to understand mechanisms involved in these lesions. Thus, the present study aimed to analyze and compare the immunohistochemical expression of PI3K and PTEN in odontogenic keratocysts and ameloblastomas. The sample consisted of 10 OKC and 10 AM. Immunohistochemical screening was performed using the anti-PI3K (1:400) and anti-PTEN (1:400). Mean ± SEM of the calculated cell counts and histories were expressed and analyzed by the Mann-Whitney test, followed by Dunn's post-test and correlated using Spearman's correlation. The categorical data were expressed as absolute frequency and compared using Fisher's Exact or Pearson's Chi-square test. Immunohistochemical analysis showed positive immunoblot in all cases of the sample. The total nuclear-stained cells for OKC PTEN were 39.21 ± 12.38 immunopositive cells and AM were 93.60 ± 2.45 (p <0.001). The cytoplasmic immunoexpression of PTEN to OKC was 87.35 ± 5.72 cells immunolabelled and 99.30 ± 0.48 for AM (p = 0.023). The comparison between the histoscore nucleus of PTEN in the OKC (4.90 ± 1.36) and in the AM (11.20 ± 0.53) (p=0.003), also evidencing statistical significance in the comparison of histoscore cytoplasm (p=0.011). The correlation between the percentages of PI3K and PTEN immunoblotting in OKC showed a statistically significant relationship between the percentage of cytoplasmic immunoexpression (p=0.019). Considering the results obtained in this research, it can be concluded that PI3K and PTEN are present in the epithelial constituents of OKC and AM. It is suggested that the PI3K / PTEN pathway may be active in OKC because the negative correlation of PI3K and PTEN is found in this odontogenic cyst.Os cistos odontogênicos são lesões relativamente comuns que causam destruição óssea nos maxilares. São classificados conforme sua origem em: cistos de desenvolvimento, incluindo o ceratocisto odontogênico (OKC), ou em cistos inflamatórios. Já os tumores odontogênicos correspondem a um grupo complexo de lesões de diversos tipos histopatológicos e comportamentos clínicos, sendo classificados conforme sua origem. Dentre os tumores de origem epitelial odontogênica, o ameloblastoma (AM) é um tumor frequentemente significativo, devido ao seu crescimento lento e sua característica clínica de invasividade local. A patogênese dos cistos e tumores odontogênicos ainda é pouco elucidada e estudos buscam identificar mecanismos e vias envolvidas na formação e progressão dessas lesões. Nesse contexto, a via PI3K/AKT/PTEN tem sido analisada em algumas lesões odontogênicas, buscando compreender mecanismos envolvidos nestas. Assim, o presente estudo objetivou analisar a expressão imunohistoquímica de PI3K e PTEN em OKC e AM. A amostra foi constituída por 10 OKC e 10 AM. A verificação imunohistoquímica foi realizada utilizando anti-PI3K (1:400) e anti-PTEN (1:400). Foram expressas as médias ± EPM das contagens das células e dos histoscores calculados, os quais foram analisados pelo teste de Mann-Whitney, seguido do pós-teste de Dunn e correlacionados usando a correlação de Spearman. Os dados categóricos foram expressos em frequência absoluta e comparados pelo teste Exato de Fisher ou Qui-quadrado de Pearson. A análise imunohistoquímica evidenciou imunomarcação positiva em todos os casos da amostra. O total de células com marcação nuclear para PTEN de OKC foram 39,21±12,38 e de AM foram 93,60±2,45 (p< 0,001). A imunoexpressão citoplasmática de PTEN para OKC foram de 87,35±5,72 células imunomarcadas e de 99,30±0,48 para os AM (p=0,023). A comparação do histoscore núcleo de PTEN entre os OKC (4,90±1,36) e os AM (11,20±0,53) evidenciou significância estatística (p=0,003), assim como na comparação do histoscore citoplasma de PTEN (p=0,011) e na correlação entre as porcentagens de imunomarcação citoplasmática de PI3K e PTEN nos OKC (p=0,019). Pode-se concluir que PI3K e PTEN estão presentes nos constituintes epiteliais dos OKC e AM. Sugere-se que a via PI3K/PTEN pode está ativa em OKC em virtude da correlação negativa de PI3K e PTEN ser encontrada nesse cisto odontogênico.AmeloblastomaImuno-HistoquímicaAvaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomasEvaluation of PI3K and PTEN immunoexpression in odontogenic keratocysts and ameloblastomasinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccessORIGINAL2018_dis_sgfeitosa.pdf2018_dis_sgfeitosa.pdfapplication/pdf1828966http://repositorio.ufc.br/bitstream/riufc/30029/1/2018_dis_sgfeitosa.pdfe87b1650330811e9ae346d46e5b86ce2MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://repositorio.ufc.br/bitstream/riufc/30029/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52riufc/300292019-01-31 15:31:04.376oai:repositorio.ufc.br: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Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2019-01-31T18:31:04Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
dc.title.en.pt_BR.fl_str_mv Evaluation of PI3K and PTEN immunoexpression in odontogenic keratocysts and ameloblastomas
title Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
spellingShingle Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
Feitosa, Sthefane Gomes
Ameloblastoma
Imuno-Histoquímica
title_short Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
title_full Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
title_fullStr Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
title_full_unstemmed Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
title_sort Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas
author Feitosa, Sthefane Gomes
author_facet Feitosa, Sthefane Gomes
author_role author
dc.contributor.author.fl_str_mv Feitosa, Sthefane Gomes
dc.contributor.advisor1.fl_str_mv Pereira, Karuza Maria Alves
contributor_str_mv Pereira, Karuza Maria Alves
dc.subject.por.fl_str_mv Ameloblastoma
Imuno-Histoquímica
topic Ameloblastoma
Imuno-Histoquímica
description Odontogenic cysts are relatively common lesions that cause bone destruction in the jaws. They are classified according to their origin in: developmental cysts, including odontogenic keratocyst (OKC), or in inflammatory cysts. Odontogenic tumors correspond to a complex group of lesions of different histopathological types and clinical behaviors, being classified according to their origin. Among tumors of odontogenic epithelial origin, ameloblastoma (AM) is often significant, tumor due to its slow growth and clinical feature of local invasiveness. The pathogenesis of odontogenic cysts and tumors is still little elucidated and studies aim to identify mechanisms and pathways involved in the formation and progression of these lesions. In this context, the PI3K / AKT / PTEN pathway has been analyzed in some odontogenic cysts and tumors in order to understand mechanisms involved in these lesions. Thus, the present study aimed to analyze and compare the immunohistochemical expression of PI3K and PTEN in odontogenic keratocysts and ameloblastomas. The sample consisted of 10 OKC and 10 AM. Immunohistochemical screening was performed using the anti-PI3K (1:400) and anti-PTEN (1:400). Mean ± SEM of the calculated cell counts and histories were expressed and analyzed by the Mann-Whitney test, followed by Dunn's post-test and correlated using Spearman's correlation. The categorical data were expressed as absolute frequency and compared using Fisher's Exact or Pearson's Chi-square test. Immunohistochemical analysis showed positive immunoblot in all cases of the sample. The total nuclear-stained cells for OKC PTEN were 39.21 ± 12.38 immunopositive cells and AM were 93.60 ± 2.45 (p <0.001). The cytoplasmic immunoexpression of PTEN to OKC was 87.35 ± 5.72 cells immunolabelled and 99.30 ± 0.48 for AM (p = 0.023). The comparison between the histoscore nucleus of PTEN in the OKC (4.90 ± 1.36) and in the AM (11.20 ± 0.53) (p=0.003), also evidencing statistical significance in the comparison of histoscore cytoplasm (p=0.011). The correlation between the percentages of PI3K and PTEN immunoblotting in OKC showed a statistically significant relationship between the percentage of cytoplasmic immunoexpression (p=0.019). Considering the results obtained in this research, it can be concluded that PI3K and PTEN are present in the epithelial constituents of OKC and AM. It is suggested that the PI3K / PTEN pathway may be active in OKC because the negative correlation of PI3K and PTEN is found in this odontogenic cyst.
publishDate 2018
dc.date.accessioned.fl_str_mv 2018-03-02T17:37:10Z
dc.date.available.fl_str_mv 2018-03-02T17:37:10Z
dc.date.issued.fl_str_mv 2018-02-15
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dc.identifier.citation.fl_str_mv FEITOSA, S. G. Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas. 2018. 67 f. Dissertação (Mestrado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2018.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufc.br/handle/riufc/30029
identifier_str_mv FEITOSA, S. G. Avaliação da imunoexpressão de PI3K e PTEN em ceratocistos odontogênicos e ameloblastomas. 2018. 67 f. Dissertação (Mestrado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2018.
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