Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S1676-24442008000200007 http://repositorio.unifesp.br/handle/11600/4314 |
Resumo: | BACKGROUND: Osteosarcomas (OS), the most frequent primary malignant bone tumors, have aggressive local behavior and high rate of metastatization. The events that allow tumor growth and dissemination are still controversial. The studies about carcinogenesis and tumor progression in this neoplasia, which are based on c-erb-B2, P-glycoprotein (P-gp) and p53 immunoexpression, show conflicting results as to the real prognostic value and its correlations with histological parameters. Anaplasia in childhood neoplasias is a histological parameter of tumor aggressiveness and chemoresistance. In primary or metastatic OS, its meaning remains controversial. On the other hand, in other human neoplasias, c-erb-B2 expression is associated with p53, nuclear grade and other aggressiveness parameters. OBJECTIVE: The aim of the present study was to evaluate p53, c-erb-B2 and P-gp immunoexpression in OS, correlating the parameters with the presence of anaplasia. METHODS: This study included 96 pre-chemotherapy biopsies in patients with high-grade OS diagnosed between 1991 and 2000. The immunohistochemical evaluation of p53 and c-erb-B2 was carried out with the streptavidin-biotin-peroxidase technique. Cases were considered positive when there was immunoexpression in 10% or more neoplastic cells. Only membrane staining (for c-erb-B2 and P-gp), and nuclear staining (for p53) were considered positive. Anaplasia was defined as Wilms' tumor, and considered present or absent. RESULTS: Anaplasia was present in 29 out of 82 cases (35.36%); p53 immunoexpression was detected in 25 out of 60 cases (36.23%); P-gp, in 30 out of 73 cases (41.1%); and c-erb-B2, in 22 out of 55 cases (40%). The results demonstrated an association between c-erb-B2 and p53 immunoexpression (p = 0.042), p53 and parameter of anaplasia (p = 0.015), anaplasia and P-gp (p = 0.034). CONCLUSIONS: The p53, c-erb-B2 and P-gp immunoexpression is relatively frequent in high-grade, metastatic and non-metastatic OS. The results reinforce the hypotheses that in the presence of anaplasia adverse events may occur simultaneously in this neoplasm. Anaplasia may become a histological marker for P-gp and/or p53 status in some high-grade OS, and it may indicate chemoresistance. There was no positive association between p53 and P-gp. |
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Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasiaP-glycoprotein, erb2 and p53 expression in high-grade human osteosarcomas and their correlation with anaplasiaOsteosarcomaImmunohistochemistryBone tumorBone neoplasmHistological markersOsteossarcomaImuno-histoquímicaTumores ósseosNeoplasias ósseasMarcadores histológicosBACKGROUND: Osteosarcomas (OS), the most frequent primary malignant bone tumors, have aggressive local behavior and high rate of metastatization. The events that allow tumor growth and dissemination are still controversial. The studies about carcinogenesis and tumor progression in this neoplasia, which are based on c-erb-B2, P-glycoprotein (P-gp) and p53 immunoexpression, show conflicting results as to the real prognostic value and its correlations with histological parameters. Anaplasia in childhood neoplasias is a histological parameter of tumor aggressiveness and chemoresistance. In primary or metastatic OS, its meaning remains controversial. On the other hand, in other human neoplasias, c-erb-B2 expression is associated with p53, nuclear grade and other aggressiveness parameters. OBJECTIVE: The aim of the present study was to evaluate p53, c-erb-B2 and P-gp immunoexpression in OS, correlating the parameters with the presence of anaplasia. METHODS: This study included 96 pre-chemotherapy biopsies in patients with high-grade OS diagnosed between 1991 and 2000. The immunohistochemical evaluation of p53 and c-erb-B2 was carried out with the streptavidin-biotin-peroxidase technique. Cases were considered positive when there was immunoexpression in 10% or more neoplastic cells. Only membrane staining (for c-erb-B2 and P-gp), and nuclear staining (for p53) were considered positive. Anaplasia was defined as Wilms' tumor, and considered present or absent. RESULTS: Anaplasia was present in 29 out of 82 cases (35.36%); p53 immunoexpression was detected in 25 out of 60 cases (36.23%); P-gp, in 30 out of 73 cases (41.1%); and c-erb-B2, in 22 out of 55 cases (40%). The results demonstrated an association between c-erb-B2 and p53 immunoexpression (p = 0.042), p53 and parameter of anaplasia (p = 0.015), anaplasia and P-gp (p = 0.034). CONCLUSIONS: The p53, c-erb-B2 and P-gp immunoexpression is relatively frequent in high-grade, metastatic and non-metastatic OS. The results reinforce the hypotheses that in the presence of anaplasia adverse events may occur simultaneously in this neoplasm. Anaplasia may become a histological marker for P-gp and/or p53 status in some high-grade OS, and it may indicate chemoresistance. There was no positive association between p53 and P-gp.INTRODUÇÃO: Osteossarcoma (OS), o mais freqüente tumor primário maligno do osso, tem comportamento local agressivo e alto índice de disseminação sistêmica. Os eventos que permitem o crescimento e a disseminação tumoral ainda permanecem controversos. Os estudos sobre a carcinogênese e a progressão dessa neoplasia, com base na imunoexpressão de c-erb-B2, P-glicoproteína (P-gp) e p53, apresentam resultados conflitantes acerca do real valor prognóstico e suas correlações com parâmetros histológicos. A anaplasia, em neoplasias na infância, constitui parâmetro histológico de agressividade tumoral e quimiorresistência. Nos OS primários ou metastáticos, seu significado permanece controverso. Por outro lado, em outras neoplasias humanas, a expressão do c-erb-B2 relaciona-se com p53, grau nuclear e outros parâmetros de agressividade. OBJETIVO: Avaliar a imunoexpressão de p53, c-erb-B2 e P-gp em OS, correlacionando os parâmetros entre si e com a presença de anaplasia. MÉTODO: O estudo incluiu 96 biópsias pré-quimioterapia de pacientes com OS de alto grau, diagnosticados entre 1991 e 2000. A pesquisa imuno-histoquímica de p53, P-gp e c-erb-B2 foi feita pela técnica da estreptoavidina-biotina-peroxidase. Foram considerados positivos os casos onde havia imunoexpressão em 10% ou mais das células neoplásicas. Somente colorações membranosa (para cerb-B2 e P-gp) e nuclear (para p53) foram consideradas positivas. Anaplasia foi definida como no tumor de Wilms, sendo considerada presente ou ausente. RESULTADOS: Anaplasia pôde ser avaliada em 82/96 casos, estando presente em 29 (35,36%). Imunoexpressão de p53 foi detectada em 25 dos 60 casos (36,23%); de P-gp, em 30 dos 73 casos (41,1%); e de c-erb-B2, em 22 dos 55 casos (40%). Os resultados demonstraram associação entre as imunoexpressões de c-erb-B2 e p53 (p = 0,042), p53 e o parâmetro anaplasia (p = 0,015), anaplasia e Pg (p = 0.034) CONCLUSÕES: A imunoexpressão de p53, c-erb-B2 e P-gp é evento relativamente freqüente em OS de alto grau, metastáticos e não-metastáticos ao diagnóstico. Os resultados reforçam a hipótese de que nessa neoplasia na presença de anaplasia ocorrem simultaneamente eventos adversos, que atuam conjuntamente. A anaplasia constitui marcador histológico do status da P-gp e/ou do p53 em parte dos OS de alto grau e nestes talvez seja indicativa de quimiorresistência. Não houve associação positiva entre p53 e P-gp.Universidade Federal de São Paulo (UNIFESP) Departamento de PatologiaUNIFESP Departamento de PediatriaUNIFESP Departamento de OrtopediaUNIFESP Grupo de Apoio ao Adolescente e Criança com Câncer Departamento de Genética do Instituto de OncologiaUNIFESP, Depto. de PatologiaUNIFESP, Depto. de PediatriaUNIFESP, Depto. de OrtopediaUNIFESP, Grupo de Apoio ao Adolescente e Criança com Câncer Depto. de Genética do Instituto de OncologiaSciELOSociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de CitopatologiaUniversidade Federal de São Paulo (UNIFESP)Alves, Maria Teresa de Seixas [UNIFESP]Miiji, Luciana Nakao Odashiro [UNIFESP]Marinho, Larissa Cardoso [UNIFESP]Petrilli, Antonio Sergio [UNIFESP]Garcia Filho, Reynaldo Jesus [UNIFESP]Tolledo, Silvia Caminada [UNIFESP]Patricio, Francy Reis da Silva [UNIFESP]2015-06-14T13:38:29Z2015-06-14T13:38:29Z2008-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion107-114application/pdfhttp://dx.doi.org/10.1590/S1676-24442008000200007Jornal Brasileiro de Patologia e Medicina Laboratorial. Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia, v. 44, n. 2, p. 107-114, 2008.10.1590/S1676-24442008000200007S1676-24442008000200007.pdf1676-2444S1676-24442008000200007http://repositorio.unifesp.br/handle/11600/4314porJornal Brasileiro de Patologia e Medicina Laboratorialinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-06T08:41:50Zoai:repositorio.unifesp.br/:11600/4314Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-06T08:41:50Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia P-glycoprotein, erb2 and p53 expression in high-grade human osteosarcomas and their correlation with anaplasia |
title |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
spellingShingle |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia Alves, Maria Teresa de Seixas [UNIFESP] Osteosarcoma Immunohistochemistry Bone tumor Bone neoplasm Histological markers Osteossarcoma Imuno-histoquímica Tumores ósseos Neoplasias ósseas Marcadores histológicos |
title_short |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
title_full |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
title_fullStr |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
title_full_unstemmed |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
title_sort |
Osteossarcomas humanos de alto grau: imunoexpressão de p53, erb-2 e P-glicoproteína, e correlação com o parâmetro anaplasia |
author |
Alves, Maria Teresa de Seixas [UNIFESP] |
author_facet |
Alves, Maria Teresa de Seixas [UNIFESP] Miiji, Luciana Nakao Odashiro [UNIFESP] Marinho, Larissa Cardoso [UNIFESP] Petrilli, Antonio Sergio [UNIFESP] Garcia Filho, Reynaldo Jesus [UNIFESP] Tolledo, Silvia Caminada [UNIFESP] Patricio, Francy Reis da Silva [UNIFESP] |
author_role |
author |
author2 |
Miiji, Luciana Nakao Odashiro [UNIFESP] Marinho, Larissa Cardoso [UNIFESP] Petrilli, Antonio Sergio [UNIFESP] Garcia Filho, Reynaldo Jesus [UNIFESP] Tolledo, Silvia Caminada [UNIFESP] Patricio, Francy Reis da Silva [UNIFESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Alves, Maria Teresa de Seixas [UNIFESP] Miiji, Luciana Nakao Odashiro [UNIFESP] Marinho, Larissa Cardoso [UNIFESP] Petrilli, Antonio Sergio [UNIFESP] Garcia Filho, Reynaldo Jesus [UNIFESP] Tolledo, Silvia Caminada [UNIFESP] Patricio, Francy Reis da Silva [UNIFESP] |
dc.subject.por.fl_str_mv |
Osteosarcoma Immunohistochemistry Bone tumor Bone neoplasm Histological markers Osteossarcoma Imuno-histoquímica Tumores ósseos Neoplasias ósseas Marcadores histológicos |
topic |
Osteosarcoma Immunohistochemistry Bone tumor Bone neoplasm Histological markers Osteossarcoma Imuno-histoquímica Tumores ósseos Neoplasias ósseas Marcadores histológicos |
description |
BACKGROUND: Osteosarcomas (OS), the most frequent primary malignant bone tumors, have aggressive local behavior and high rate of metastatization. The events that allow tumor growth and dissemination are still controversial. The studies about carcinogenesis and tumor progression in this neoplasia, which are based on c-erb-B2, P-glycoprotein (P-gp) and p53 immunoexpression, show conflicting results as to the real prognostic value and its correlations with histological parameters. Anaplasia in childhood neoplasias is a histological parameter of tumor aggressiveness and chemoresistance. In primary or metastatic OS, its meaning remains controversial. On the other hand, in other human neoplasias, c-erb-B2 expression is associated with p53, nuclear grade and other aggressiveness parameters. OBJECTIVE: The aim of the present study was to evaluate p53, c-erb-B2 and P-gp immunoexpression in OS, correlating the parameters with the presence of anaplasia. METHODS: This study included 96 pre-chemotherapy biopsies in patients with high-grade OS diagnosed between 1991 and 2000. The immunohistochemical evaluation of p53 and c-erb-B2 was carried out with the streptavidin-biotin-peroxidase technique. Cases were considered positive when there was immunoexpression in 10% or more neoplastic cells. Only membrane staining (for c-erb-B2 and P-gp), and nuclear staining (for p53) were considered positive. Anaplasia was defined as Wilms' tumor, and considered present or absent. RESULTS: Anaplasia was present in 29 out of 82 cases (35.36%); p53 immunoexpression was detected in 25 out of 60 cases (36.23%); P-gp, in 30 out of 73 cases (41.1%); and c-erb-B2, in 22 out of 55 cases (40%). The results demonstrated an association between c-erb-B2 and p53 immunoexpression (p = 0.042), p53 and parameter of anaplasia (p = 0.015), anaplasia and P-gp (p = 0.034). CONCLUSIONS: The p53, c-erb-B2 and P-gp immunoexpression is relatively frequent in high-grade, metastatic and non-metastatic OS. The results reinforce the hypotheses that in the presence of anaplasia adverse events may occur simultaneously in this neoplasm. Anaplasia may become a histological marker for P-gp and/or p53 status in some high-grade OS, and it may indicate chemoresistance. There was no positive association between p53 and P-gp. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-04-01 2015-06-14T13:38:29Z 2015-06-14T13:38:29Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S1676-24442008000200007 Jornal Brasileiro de Patologia e Medicina Laboratorial. Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia, v. 44, n. 2, p. 107-114, 2008. 10.1590/S1676-24442008000200007 S1676-24442008000200007.pdf 1676-2444 S1676-24442008000200007 http://repositorio.unifesp.br/handle/11600/4314 |
url |
http://dx.doi.org/10.1590/S1676-24442008000200007 http://repositorio.unifesp.br/handle/11600/4314 |
identifier_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial. Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia, v. 44, n. 2, p. 107-114, 2008. 10.1590/S1676-24442008000200007 S1676-24442008000200007.pdf 1676-2444 S1676-24442008000200007 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial |
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info:eu-repo/semantics/openAccess |
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openAccess |
dc.format.none.fl_str_mv |
107-114 application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268426805313536 |