MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors

Detalhes bibliográficos
Autor(a) principal: Yoshimoto, Maisa [UNIFESP]
Data de Publicação: 1999
Outros Autores: Toledo, Silvia Regina Caminada de [UNIFESP], Caran, Eliana Maria Monteiro [UNIFESP], Seixas, Maria Teresa de [UNIFESP], Lee, Maria Lucia de Martino [UNIFESP], Abib, Simone de Campos Vieira [UNIFESP], Vianna, Sonia Maria Rossi, Schettini, Sergio Tomaz [UNIFESP], Andrade, Joyce Anderson Duffles [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/S0002-9440(10)65457-0
http://repositorio.unifesp.br/handle/11600/26163
Resumo: Neuroblastoma is the second most common solid tumor occurring in children. Amplification of the MYCN oncogene is associated with poor prognosis. To identify neuroblastoma tumors with MYCN amplification, we studied the number of copies of MYCN in interphase cells by fluorescence in situ hybridization in 20 neuroblastoma patients. MYCN amplification appeared in 7 tumor specimens. Interphase and metaphase studies showed a tumor cell population with both forms of amplification, double minutes and homogeneously staining regions, in two patients. These patients showed a smaller tumor cell subpopulation with the presence of more than one homogeneously staining region, suggesting that gene amplification was undergoing karyotype evolution.
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spelling MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumorsNeuroblastoma is the second most common solid tumor occurring in children. Amplification of the MYCN oncogene is associated with poor prognosis. To identify neuroblastoma tumors with MYCN amplification, we studied the number of copies of MYCN in interphase cells by fluorescence in situ hybridization in 20 neuroblastoma patients. MYCN amplification appeared in 7 tumor specimens. Interphase and metaphase studies showed a tumor cell population with both forms of amplification, double minutes and homogeneously staining regions, in two patients. These patients showed a smaller tumor cell subpopulation with the presence of more than one homogeneously staining region, suggesting that gene amplification was undergoing karyotype evolution.Universidade Federal de São Paulo, Dept Morphol, Div Genet, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pathol, Div Med Pathol, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Surg, Div Pediat Surg, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Inst Oncol Pediat, Escola Paulista Med, São Paulo, BrazilHosp Servidor Publ Estadual, Div Pediat Oncol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol, Div Genet, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pathol, Div Med Pathol, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Surg, Div Pediat Surg, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Inst Oncol Pediat, Escola Paulista Med, São Paulo, BrazilWeb of ScienceAmer Soc Investigative Pathology, IncUniversidade Federal de São Paulo (UNIFESP)Hosp Servidor Publ EstadualYoshimoto, Maisa [UNIFESP]Toledo, Silvia Regina Caminada de [UNIFESP]Caran, Eliana Maria Monteiro [UNIFESP]Seixas, Maria Teresa de [UNIFESP]Lee, Maria Lucia de Martino [UNIFESP]Abib, Simone de Campos Vieira [UNIFESP]Vianna, Sonia Maria RossiSchettini, Sergio Tomaz [UNIFESP]Andrade, Joyce Anderson Duffles [UNIFESP]2016-01-24T12:30:54Z2016-01-24T12:30:54Z1999-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1439-1443http://dx.doi.org/10.1016/S0002-9440(10)65457-0American Journal of Pathology. Baltimore: Amer Soc Investigative Pathology, Inc, v. 155, n. 5, p. 1439-1443, 1999.10.1016/S0002-9440(10)65457-00002-9440http://repositorio.unifesp.br/handle/11600/26163WOS:000083587600007engAmerican Journal of Pathologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-03-16T15:49:48Zoai:repositorio.unifesp.br/:11600/26163Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-03-16T15:49:48Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
title MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
spellingShingle MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
Yoshimoto, Maisa [UNIFESP]
title_short MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
title_full MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
title_fullStr MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
title_full_unstemmed MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
title_sort MYCN gene amplification - Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors
author Yoshimoto, Maisa [UNIFESP]
author_facet Yoshimoto, Maisa [UNIFESP]
Toledo, Silvia Regina Caminada de [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Seixas, Maria Teresa de [UNIFESP]
Lee, Maria Lucia de Martino [UNIFESP]
Abib, Simone de Campos Vieira [UNIFESP]
Vianna, Sonia Maria Rossi
Schettini, Sergio Tomaz [UNIFESP]
Andrade, Joyce Anderson Duffles [UNIFESP]
author_role author
author2 Toledo, Silvia Regina Caminada de [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Seixas, Maria Teresa de [UNIFESP]
Lee, Maria Lucia de Martino [UNIFESP]
Abib, Simone de Campos Vieira [UNIFESP]
Vianna, Sonia Maria Rossi
Schettini, Sergio Tomaz [UNIFESP]
Andrade, Joyce Anderson Duffles [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Hosp Servidor Publ Estadual
dc.contributor.author.fl_str_mv Yoshimoto, Maisa [UNIFESP]
Toledo, Silvia Regina Caminada de [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Seixas, Maria Teresa de [UNIFESP]
Lee, Maria Lucia de Martino [UNIFESP]
Abib, Simone de Campos Vieira [UNIFESP]
Vianna, Sonia Maria Rossi
Schettini, Sergio Tomaz [UNIFESP]
Andrade, Joyce Anderson Duffles [UNIFESP]
description Neuroblastoma is the second most common solid tumor occurring in children. Amplification of the MYCN oncogene is associated with poor prognosis. To identify neuroblastoma tumors with MYCN amplification, we studied the number of copies of MYCN in interphase cells by fluorescence in situ hybridization in 20 neuroblastoma patients. MYCN amplification appeared in 7 tumor specimens. Interphase and metaphase studies showed a tumor cell population with both forms of amplification, double minutes and homogeneously staining regions, in two patients. These patients showed a smaller tumor cell subpopulation with the presence of more than one homogeneously staining region, suggesting that gene amplification was undergoing karyotype evolution.
publishDate 1999
dc.date.none.fl_str_mv 1999-11-01
2016-01-24T12:30:54Z
2016-01-24T12:30:54Z
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/10.1016/S0002-9440(10)65457-0
American Journal of Pathology. Baltimore: Amer Soc Investigative Pathology, Inc, v. 155, n. 5, p. 1439-1443, 1999.
10.1016/S0002-9440(10)65457-0
0002-9440
http://repositorio.unifesp.br/handle/11600/26163
WOS:000083587600007
url http://dx.doi.org/10.1016/S0002-9440(10)65457-0
http://repositorio.unifesp.br/handle/11600/26163
identifier_str_mv American Journal of Pathology. Baltimore: Amer Soc Investigative Pathology, Inc, v. 155, n. 5, p. 1439-1443, 1999.
10.1016/S0002-9440(10)65457-0
0002-9440
WOS:000083587600007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv American Journal of Pathology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1439-1443
dc.publisher.none.fl_str_mv Amer Soc Investigative Pathology, Inc
publisher.none.fl_str_mv Amer Soc Investigative Pathology, Inc
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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