Histopathological features and P-glycoprotein expression in retinoblastoma
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1814268361382559744 |