Histopathological features and P-glycoprotein expression in retinoblastoma

Detalhes bibliográficos
Autor(a) principal: Souza Filho, João Pessoa de [UNIFESP]
Data de Publicação: 2005
Outros Autores: Corrêa, Zélia Maria da Silva [UNIFESP], Odashiro, Alexandre N. [UNIFESP, Coutinho, Anamaria Baptista [UNIFESP, Martins, Maria Cristina [UNIFESP], Erwenne, Clélia Maria [UNIFESP], Burnier Júnior, Miguel Noel Nascente [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1167/iovs.04-1290
http://repositorio.unifesp.br/handle/11600/28482
Resumo: PURPOSE. To investigate the expression of P- glycoprotein (P-gp) in retinoblastoma specimens enucleated as a primary treatment or after conservative treatment and to correlate this expression with histopathological tumor features.METHODS. Retrospective analysis was performed on retinoblastoma specimens obtained consecutively between 1993 and 2003 by enucleation either as primary treatment ( group I) or after the failure of conservative treatment ( group II). Sections from the formalin-fixed, paraffin-embedded specimens were stained with hematoxylin and eosin. Group I tumor differentiation was classified according to the percentage of Flexner-Wintersteiner rosettes. Group II tumors, categorized as viable-appearing, regressed with a well-differentiated component (WDC), and regressed. Other features, such as choroidal and optic nerve invasion, were evaluated. P-gp expression was graded semiquantitatively as negative, low, or high. Variables were statistically analyzed by chi(2) and Student's t-tests.RESULTS. Histopathological assessment of group I revealed 65% moderately differentiated tumors, 30% well differentiated, and 5% poorly differentiated. Fifteen percent had optic nerve tumor invasion only, 20% choroidal invasion only, and 55% both choroidal and optic nerve invasion. Group II had 62.5% well-differentiated, regressed tumors; 25% had regressed tumors replaced by glial scarring; and 12.5% had tumors containing viable, poorly differentiated cells. Approximately 18% had choroidal tumor invasion only, 6.3% optic nerve tumor invasion only, and 6.3% simultaneous optic nerve and choroidal invasion. P- gp expression was observed in 60% of group I and 66.6% of group II. All P-gp-positive cases in group II had a high expression. P- gp was also expressed by 81.2% of well-differentiated tumors.CONCLUSIONS. P- gp was expressed more frequently by well-differentiated retinoblastomas, especially those treated by chemotherapy before enucleation. This finding could be related to treatment failure.
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spelling Histopathological features and P-glycoprotein expression in retinoblastomaPURPOSE. To investigate the expression of P- glycoprotein (P-gp) in retinoblastoma specimens enucleated as a primary treatment or after conservative treatment and to correlate this expression with histopathological tumor features.METHODS. Retrospective analysis was performed on retinoblastoma specimens obtained consecutively between 1993 and 2003 by enucleation either as primary treatment ( group I) or after the failure of conservative treatment ( group II). Sections from the formalin-fixed, paraffin-embedded specimens were stained with hematoxylin and eosin. Group I tumor differentiation was classified according to the percentage of Flexner-Wintersteiner rosettes. Group II tumors, categorized as viable-appearing, regressed with a well-differentiated component (WDC), and regressed. Other features, such as choroidal and optic nerve invasion, were evaluated. P-gp expression was graded semiquantitatively as negative, low, or high. Variables were statistically analyzed by chi(2) and Student's t-tests.RESULTS. Histopathological assessment of group I revealed 65% moderately differentiated tumors, 30% well differentiated, and 5% poorly differentiated. Fifteen percent had optic nerve tumor invasion only, 20% choroidal invasion only, and 55% both choroidal and optic nerve invasion. Group II had 62.5% well-differentiated, regressed tumors; 25% had regressed tumors replaced by glial scarring; and 12.5% had tumors containing viable, poorly differentiated cells. Approximately 18% had choroidal tumor invasion only, 6.3% optic nerve tumor invasion only, and 6.3% simultaneous optic nerve and choroidal invasion. P- gp expression was observed in 60% of group I and 66.6% of group II. All P-gp-positive cases in group II had a high expression. P- gp was also expressed by 81.2% of well-differentiated tumors.CONCLUSIONS. P- gp was expressed more frequently by well-differentiated retinoblastomas, especially those treated by chemotherapy before enucleation. This finding could be related to treatment failure.Universidade Federal de São Paulo, Dept Ophthalmol, São Paulo, BrazilMcGill Univ, Dept Ophthalmol, Henry C Witelson Ocular Pathol Lab, Montreal, PQ H3A 2T5, CanadaUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, BrazilWeb of ScienceAssoc Research Vision Ophthalmology IncUniversidade Federal de São Paulo (UNIFESP)McGill UnivSouza Filho, João Pessoa de [UNIFESP]Corrêa, Zélia Maria da Silva [UNIFESP]Odashiro, Alexandre N. [UNIFESPCoutinho, Anamaria Baptista [UNIFESPMartins, Maria Cristina [UNIFESP]Erwenne, Clélia Maria [UNIFESP]Burnier Júnior, Miguel Noel Nascente [UNIFESP]2016-01-24T12:38:05Z2016-01-24T12:38:05Z2005-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion3478-3483http://dx.doi.org/10.1167/iovs.04-1290Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 10, p. 3478-3483, 2005.10.1167/iovs.04-12900146-0404http://repositorio.unifesp.br/handle/11600/28482WOS:000232112900002engInvestigative Ophthalmology & Visual Scienceinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-05-05T11:13:22Zoai:repositorio.unifesp.br/:11600/28482Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-05-05T11:13:22Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Histopathological features and P-glycoprotein expression in retinoblastoma
title Histopathological features and P-glycoprotein expression in retinoblastoma
spellingShingle Histopathological features and P-glycoprotein expression in retinoblastoma
Souza Filho, João Pessoa de [UNIFESP]
title_short Histopathological features and P-glycoprotein expression in retinoblastoma
title_full Histopathological features and P-glycoprotein expression in retinoblastoma
title_fullStr Histopathological features and P-glycoprotein expression in retinoblastoma
title_full_unstemmed Histopathological features and P-glycoprotein expression in retinoblastoma
title_sort Histopathological features and P-glycoprotein expression in retinoblastoma
author Souza Filho, João Pessoa de [UNIFESP]
author_facet Souza Filho, João Pessoa de [UNIFESP]
Corrêa, Zélia Maria da Silva [UNIFESP]
Odashiro, Alexandre N. [UNIFESP
Coutinho, Anamaria Baptista [UNIFESP
Martins, Maria Cristina [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
Burnier Júnior, Miguel Noel Nascente [UNIFESP]
author_role author
author2 Corrêa, Zélia Maria da Silva [UNIFESP]
Odashiro, Alexandre N. [UNIFESP
Coutinho, Anamaria Baptista [UNIFESP
Martins, Maria Cristina [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
Burnier Júnior, Miguel Noel Nascente [UNIFESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
McGill Univ
dc.contributor.author.fl_str_mv Souza Filho, João Pessoa de [UNIFESP]
Corrêa, Zélia Maria da Silva [UNIFESP]
Odashiro, Alexandre N. [UNIFESP
Coutinho, Anamaria Baptista [UNIFESP
Martins, Maria Cristina [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
Burnier Júnior, Miguel Noel Nascente [UNIFESP]
description PURPOSE. To investigate the expression of P- glycoprotein (P-gp) in retinoblastoma specimens enucleated as a primary treatment or after conservative treatment and to correlate this expression with histopathological tumor features.METHODS. Retrospective analysis was performed on retinoblastoma specimens obtained consecutively between 1993 and 2003 by enucleation either as primary treatment ( group I) or after the failure of conservative treatment ( group II). Sections from the formalin-fixed, paraffin-embedded specimens were stained with hematoxylin and eosin. Group I tumor differentiation was classified according to the percentage of Flexner-Wintersteiner rosettes. Group II tumors, categorized as viable-appearing, regressed with a well-differentiated component (WDC), and regressed. Other features, such as choroidal and optic nerve invasion, were evaluated. P-gp expression was graded semiquantitatively as negative, low, or high. Variables were statistically analyzed by chi(2) and Student's t-tests.RESULTS. Histopathological assessment of group I revealed 65% moderately differentiated tumors, 30% well differentiated, and 5% poorly differentiated. Fifteen percent had optic nerve tumor invasion only, 20% choroidal invasion only, and 55% both choroidal and optic nerve invasion. Group II had 62.5% well-differentiated, regressed tumors; 25% had regressed tumors replaced by glial scarring; and 12.5% had tumors containing viable, poorly differentiated cells. Approximately 18% had choroidal tumor invasion only, 6.3% optic nerve tumor invasion only, and 6.3% simultaneous optic nerve and choroidal invasion. P- gp expression was observed in 60% of group I and 66.6% of group II. All P-gp-positive cases in group II had a high expression. P- gp was also expressed by 81.2% of well-differentiated tumors.CONCLUSIONS. P- gp was expressed more frequently by well-differentiated retinoblastomas, especially those treated by chemotherapy before enucleation. This finding could be related to treatment failure.
publishDate 2005
dc.date.none.fl_str_mv 2005-10-01
2016-01-24T12:38:05Z
2016-01-24T12:38:05Z
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/10.1167/iovs.04-1290
Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 10, p. 3478-3483, 2005.
10.1167/iovs.04-1290
0146-0404
http://repositorio.unifesp.br/handle/11600/28482
WOS:000232112900002
url http://dx.doi.org/10.1167/iovs.04-1290
http://repositorio.unifesp.br/handle/11600/28482
identifier_str_mv Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 46, n. 10, p. 3478-3483, 2005.
10.1167/iovs.04-1290
0146-0404
WOS:000232112900002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Investigative Ophthalmology & Visual Science
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 3478-3483
dc.publisher.none.fl_str_mv Assoc Research Vision Ophthalmology Inc
publisher.none.fl_str_mv Assoc Research Vision Ophthalmology 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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