Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat
- Autores
- Bergoc, Rosa
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Fil: Bergoc, Rosa. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.
The objective of this study was to evaluate the in vivo antitumor action of rosiglitazone (Rosi) alone or in combination with tamoxifen (Tam) on experimental mammary tumors induced by N-nitroso-N-methylurea (NMU) in Sprague-Dawley rats. Animals bearing mammary tumors were treated with 0.06 mg/kg/day or 0.12 mg/kg/day of Rosi orally, 1 mg/kg/day of Tam sc, or with the combined treatment (Rosi+Tam). After 25 days of treatments, the following responses were observed: 45% of tumors were responsive to 0.06 mg/kg/day of Rosi treatment, while 55% of tumors under Tam treatment responded. Results of the combined Rosi+Tam treatment indicate that 75% of tumors were responsive. Similar results were obtained with 0.12 mg/kg/day of Rosi. Apoptosis, necrosis and glandular hypersecretion were observed in Rosi-treated tumors. In all cases, the combined Rosi+Tam treatment potentiates the antitumor effect of Tam alone. No side-effect was observed after treatment at any assayed dose. - Materia
-
ARTICULO
MEDICINA
CANCER DE MAMA
FARMACOLOGIA - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- Repositorio
- Institución
- Fundación H. A. Barceló
- OAI Identificador
- oai:fbarcelo:snrd:HASH01306d5597361f65b25e7e57
Ver los metadatos del registro completo
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Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in RatBergoc, RosaARTICULOMEDICINACANCER DE MAMAFARMACOLOGIAFil: Bergoc, Rosa. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.The objective of this study was to evaluate the in vivo antitumor action of rosiglitazone (Rosi) alone or in combination with tamoxifen (Tam) on experimental mammary tumors induced by N-nitroso-N-methylurea (NMU) in Sprague-Dawley rats. Animals bearing mammary tumors were treated with 0.06 mg/kg/day or 0.12 mg/kg/day of Rosi orally, 1 mg/kg/day of Tam sc, or with the combined treatment (Rosi+Tam). After 25 days of treatments, the following responses were observed: 45% of tumors were responsive to 0.06 mg/kg/day of Rosi treatment, while 55% of tumors under Tam treatment responded. Results of the combined Rosi+Tam treatment indicate that 75% of tumors were responsive. Similar results were obtained with 0.12 mg/kg/day of Rosi. Apoptosis, necrosis and glandular hypersecretion were observed in Rosi-treated tumors. In all cases, the combined Rosi+Tam treatment potentiates the antitumor effect of Tam alone. No side-effect was observed after treatment at any assayed dose.PubMed 2006 May-Jun;26(3A):2113-222020-02-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://repositorio.barcelo.edu.ar/greenstone/collect/snrd/index/assoc/HASH0130.dir/BRC_37_MED_BA.pdfenginfo:eu-repo/semantics/openAccessreponame:Repositorio Institucional (Fundacion Barceló)instname:Fundación H. A. Barceló2025-09-18T10:48:56Zoai:fbarcelo:snrd:HASH01306d5597361f65b25e7e57instacron:BARCELOInstitucionalhttp://repositorio.barcelo.edu.ar/greenstone/cgi-bin/library.cgiUniversidad privadaNo correspondehttp://repositorio.barcelo.edu.ar/greenstone/cgi-bin/oaiserver.cgilrodriguezares@barcelo.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2025-09-18 10:48:57.702Repositorio Institucional (Fundacion Barceló) - Fundación H. A. Barcelófalse |
dc.title.none.fl_str_mv |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
title |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
spellingShingle |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat Bergoc, Rosa ARTICULO MEDICINA CANCER DE MAMA FARMACOLOGIA |
title_short |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
title_full |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
title_fullStr |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
title_full_unstemmed |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
title_sort |
Effect of Rosiglitazone on N-nitroso-N-methylurea-induced Mammary Tumors in Rat |
dc.creator.none.fl_str_mv |
Bergoc, Rosa |
author |
Bergoc, Rosa |
author_facet |
Bergoc, Rosa |
author_role |
author |
dc.subject.none.fl_str_mv |
ARTICULO MEDICINA CANCER DE MAMA FARMACOLOGIA |
topic |
ARTICULO MEDICINA CANCER DE MAMA FARMACOLOGIA |
dc.description.none.fl_txt_mv |
Fil: Bergoc, Rosa. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina. The objective of this study was to evaluate the in vivo antitumor action of rosiglitazone (Rosi) alone or in combination with tamoxifen (Tam) on experimental mammary tumors induced by N-nitroso-N-methylurea (NMU) in Sprague-Dawley rats. Animals bearing mammary tumors were treated with 0.06 mg/kg/day or 0.12 mg/kg/day of Rosi orally, 1 mg/kg/day of Tam sc, or with the combined treatment (Rosi+Tam). After 25 days of treatments, the following responses were observed: 45% of tumors were responsive to 0.06 mg/kg/day of Rosi treatment, while 55% of tumors under Tam treatment responded. Results of the combined Rosi+Tam treatment indicate that 75% of tumors were responsive. Similar results were obtained with 0.12 mg/kg/day of Rosi. Apoptosis, necrosis and glandular hypersecretion were observed in Rosi-treated tumors. In all cases, the combined Rosi+Tam treatment potentiates the antitumor effect of Tam alone. No side-effect was observed after treatment at any assayed dose. |
description |
Fil: Bergoc, Rosa. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-02-27 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://repositorio.barcelo.edu.ar/greenstone/collect/snrd/index/assoc/HASH0130.dir/BRC_37_MED_BA.pdf |
url |
http://repositorio.barcelo.edu.ar/greenstone/collect/snrd/index/assoc/HASH0130.dir/BRC_37_MED_BA.pdf |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
PubMed 2006 May-Jun;26(3A):2113-22 |
publisher.none.fl_str_mv |
PubMed 2006 May-Jun;26(3A):2113-22 |
dc.source.none.fl_str_mv |
reponame:Repositorio Institucional (Fundacion Barceló) instname:Fundación H. A. Barceló |
reponame_str |
Repositorio Institucional (Fundacion Barceló) |
collection |
Repositorio Institucional (Fundacion Barceló) |
instname_str |
Fundación H. A. Barceló |
repository.name.fl_str_mv |
Repositorio Institucional (Fundacion Barceló) - Fundación H. A. Barceló |
repository.mail.fl_str_mv |
lrodriguezares@barcelo.edu.ar |
_version_ |
1843611759741501440 |
score |
13.070432 |