The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines

Detalhes bibliográficos
Autor(a) principal: Souza, J. P. de
Data de Publicação: 2006
Outros Autores: Corrêa, Zélia Maria da Silva [UNIFESP], Marshall, J. C., Anteka, E., Coutinho, A. B., Martins, M. C., Burnier, M. N.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1038/sj.eye.6701938
http://repositorio.unifesp.br/handle/11600/28853
Resumo: Purpose To examine the effect of nepafenac, a selective cyclooxygenase-2 (COX-2) inhibitor, on the proliferation rate of two human retinoblastoma (Rb) cell lines.Methods Two human Rb cell lines (WERI-RB and Y79) were cultured. COX-2 expression in these cell lines was verified by imunocytochemical analysis of cytospin sections and Western blotting. An MTT-based proliferation assay was used to compare Rb cell growth with and without amfenac, the active metabolite of nepafenac. the averaged results per condition were recorded. the Student's t-test was used to compare results from the cells cultured with and without amfenac.Result the Y79 cell line showed a higher proliferative rate than the WERI-RB cell line. Both cell lines were negative for COX-2 expression by immunocytochemical analysis; however, both cell lines were positive for COX-2 expression by Western blot. When amfenac was added to both of the cell lines, a statistically significant reduction in proliferation was observed in both cell lines. the two Rb cell lines were positive for COX-2 only in the Western blot, indicating that they probably express low levels of COX-2, which was undetectable by immucytochemical analysis.Conclusion the selective, anti-COX-2 molecule amfenac inhibited proliferation of both tested Rb cell lines. Further trials should be undertaken to study the effect of selective COX-2 inhibitors on Rb.
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spelling The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell linesCOX-2retinoblastomanepafenaccell linesimmunocytochemistryPurpose To examine the effect of nepafenac, a selective cyclooxygenase-2 (COX-2) inhibitor, on the proliferation rate of two human retinoblastoma (Rb) cell lines.Methods Two human Rb cell lines (WERI-RB and Y79) were cultured. COX-2 expression in these cell lines was verified by imunocytochemical analysis of cytospin sections and Western blotting. An MTT-based proliferation assay was used to compare Rb cell growth with and without amfenac, the active metabolite of nepafenac. the averaged results per condition were recorded. the Student's t-test was used to compare results from the cells cultured with and without amfenac.Result the Y79 cell line showed a higher proliferative rate than the WERI-RB cell line. Both cell lines were negative for COX-2 expression by immunocytochemical analysis; however, both cell lines were positive for COX-2 expression by Western blot. When amfenac was added to both of the cell lines, a statistically significant reduction in proliferation was observed in both cell lines. the two Rb cell lines were positive for COX-2 only in the Western blot, indicating that they probably express low levels of COX-2, which was undetectable by immucytochemical analysis.Conclusion the selective, anti-COX-2 molecule amfenac inhibited proliferation of both tested Rb cell lines. Further trials should be undertaken to study the effect of selective COX-2 inhibitors on Rb.McGill Univ, Henry C Witelson Ocular Pathol Lab, Montreal, PQ, CanadaUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, SP, BrazilRetina & Oncol Serv, Dept Ophthalmol, Porto Alegre, RS, BrazilUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, SP, BrazilWeb of ScienceNature Publishing GroupMcGill UnivUniversidade Federal de São Paulo (UNIFESP)Retina & Oncol ServSouza, J. P. deCorrêa, Zélia Maria da Silva [UNIFESP]Marshall, J. C.Anteka, E.Coutinho, A. B.Martins, M. C.Burnier, M. N.2016-01-24T12:41:07Z2016-01-24T12:41:07Z2006-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion598-601http://dx.doi.org/10.1038/sj.eye.6701938Eye. London: Nature Publishing Group, v. 20, n. 5, p. 598-601, 2006.10.1038/sj.eye.67019380950-222Xhttp://repositorio.unifesp.br/handle/11600/28853WOS:000237360000016engEyeinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:41:07Zoai:repositorio.unifesp.br/:11600/28853Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:41:07Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
title The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
spellingShingle The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
Souza, J. P. de
COX-2
retinoblastoma
nepafenac
cell lines
immunocytochemistry
title_short The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
title_full The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
title_fullStr The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
title_full_unstemmed The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
title_sort The effect of a selective cyclooxygenase-2 (COX-2) inhibitor on the proliferation rate of retinoblastoma cell lines
author Souza, J. P. de
author_facet Souza, J. P. de
Corrêa, Zélia Maria da Silva [UNIFESP]
Marshall, J. C.
Anteka, E.
Coutinho, A. B.
Martins, M. C.
Burnier, M. N.
author_role author
author2 Corrêa, Zélia Maria da Silva [UNIFESP]
Marshall, J. C.
Anteka, E.
Coutinho, A. B.
Martins, M. C.
Burnier, M. N.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv McGill Univ
Universidade Federal de São Paulo (UNIFESP)
Retina & Oncol Serv
dc.contributor.author.fl_str_mv Souza, J. P. de
Corrêa, Zélia Maria da Silva [UNIFESP]
Marshall, J. C.
Anteka, E.
Coutinho, A. B.
Martins, M. C.
Burnier, M. N.
dc.subject.por.fl_str_mv COX-2
retinoblastoma
nepafenac
cell lines
immunocytochemistry
topic COX-2
retinoblastoma
nepafenac
cell lines
immunocytochemistry
description Purpose To examine the effect of nepafenac, a selective cyclooxygenase-2 (COX-2) inhibitor, on the proliferation rate of two human retinoblastoma (Rb) cell lines.Methods Two human Rb cell lines (WERI-RB and Y79) were cultured. COX-2 expression in these cell lines was verified by imunocytochemical analysis of cytospin sections and Western blotting. An MTT-based proliferation assay was used to compare Rb cell growth with and without amfenac, the active metabolite of nepafenac. the averaged results per condition were recorded. the Student's t-test was used to compare results from the cells cultured with and without amfenac.Result the Y79 cell line showed a higher proliferative rate than the WERI-RB cell line. Both cell lines were negative for COX-2 expression by immunocytochemical analysis; however, both cell lines were positive for COX-2 expression by Western blot. When amfenac was added to both of the cell lines, a statistically significant reduction in proliferation was observed in both cell lines. the two Rb cell lines were positive for COX-2 only in the Western blot, indicating that they probably express low levels of COX-2, which was undetectable by immucytochemical analysis.Conclusion the selective, anti-COX-2 molecule amfenac inhibited proliferation of both tested Rb cell lines. Further trials should be undertaken to study the effect of selective COX-2 inhibitors on Rb.
publishDate 2006
dc.date.none.fl_str_mv 2006-05-01
2016-01-24T12:41:07Z
2016-01-24T12:41:07Z
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/10.1038/sj.eye.6701938
Eye. London: Nature Publishing Group, v. 20, n. 5, p. 598-601, 2006.
10.1038/sj.eye.6701938
0950-222X
http://repositorio.unifesp.br/handle/11600/28853
WOS:000237360000016
url http://dx.doi.org/10.1038/sj.eye.6701938
http://repositorio.unifesp.br/handle/11600/28853
identifier_str_mv Eye. London: Nature Publishing Group, v. 20, n. 5, p. 598-601, 2006.
10.1038/sj.eye.6701938
0950-222X
WOS:000237360000016
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Eye
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 598-601
dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
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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