Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis

Detalhes bibliográficos
Autor(a) principal: Marques, Ricardo
Data de Publicação: 2015
Outros Autores: Vaz, Cátia, Baptista, Cláudio, Gomes, Madalena, Gama, Adelina, Alves, Gilberto, Santos, Cecilia, Schmitt, Fernando, Socorro, Sílvia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.6/7662
Resumo: Regucalcin (RGN) is a calcium-binding protein, which has been shown to be underexpressed in cancer cases. This study aimed to determine the association of RGN expression with clinicopathological parameters of human breast cancer. In addition, the role of RGN in malignancy of mammary gland using transgenic rats overexpressing the protein (Tg-RGN) was investigated. Wild-type (Wt) and Tg-RGN rats were treated with 7,12-dimethylbenz[α]anthracene (DMBA). Carcinogen-induced tumors were histologically classified and the Ki67 proliferation index was estimated. Immunohistochemistry analysis showed that RGN immunoreactivity was negatively correlated with the histological grade of breast infiltrating ductal carcinoma suggesting that progression of breast cancer is associated with loss of RGN. Tg-RGN rats displayed lower incidence of carcinogen-induced mammary gland tumors, as well as lower incidence of invasive forms. Moreover, higher proliferation was observed in non-invasive tumors of Wt animals comparatively with Tg-RGN. Overexpression of RGN was associated with diminished expression of cell-cycle inhibitors and increased expression of apoptosis inducers. Augmented activity of apoptosis effector caspase-3 was found in the mammary gland of Tg-RGN. RGN overexpression protected from carcinogen-induced mammary gland tumor development and was linked with reduced proliferation and increased apoptosis. These findings indicated the protective role of RGN in the carcinogenesis of mammary gland.
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spelling Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesisApoptosisBreast cancerCarcinogenDMBAMammary glandRegucalcinRegucalcin (RGN) is a calcium-binding protein, which has been shown to be underexpressed in cancer cases. This study aimed to determine the association of RGN expression with clinicopathological parameters of human breast cancer. In addition, the role of RGN in malignancy of mammary gland using transgenic rats overexpressing the protein (Tg-RGN) was investigated. Wild-type (Wt) and Tg-RGN rats were treated with 7,12-dimethylbenz[α]anthracene (DMBA). Carcinogen-induced tumors were histologically classified and the Ki67 proliferation index was estimated. Immunohistochemistry analysis showed that RGN immunoreactivity was negatively correlated with the histological grade of breast infiltrating ductal carcinoma suggesting that progression of breast cancer is associated with loss of RGN. Tg-RGN rats displayed lower incidence of carcinogen-induced mammary gland tumors, as well as lower incidence of invasive forms. Moreover, higher proliferation was observed in non-invasive tumors of Wt animals comparatively with Tg-RGN. Overexpression of RGN was associated with diminished expression of cell-cycle inhibitors and increased expression of apoptosis inducers. Augmented activity of apoptosis effector caspase-3 was found in the mammary gland of Tg-RGN. RGN overexpression protected from carcinogen-induced mammary gland tumor development and was linked with reduced proliferation and increased apoptosis. These findings indicated the protective role of RGN in the carcinogenesis of mammary gland.uBibliorumMarques, RicardoVaz, CátiaBaptista, CláudioGomes, MadalenaGama, AdelinaAlves, GilbertoSantos, CeciliaSchmitt, FernandoSocorro, Sílvia2019-12-04T17:00:56Z2015-01-152015-01-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.6/7662eng10.1016/j.yexcr.2014.08.007metadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-12-15T09:47:12Zoai:ubibliorum.ubi.pt:10400.6/7662Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:48:07.930594Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
title Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
spellingShingle Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
Marques, Ricardo
Apoptosis
Breast cancer
Carcinogen
DMBA
Mammary gland
Regucalcin
title_short Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
title_full Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
title_fullStr Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
title_full_unstemmed Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
title_sort Histopathological and in vivo evidence of regucalcin as a protective molecule in mammary gland carcinogenesis
author Marques, Ricardo
author_facet Marques, Ricardo
Vaz, Cátia
Baptista, Cláudio
Gomes, Madalena
Gama, Adelina
Alves, Gilberto
Santos, Cecilia
Schmitt, Fernando
Socorro, Sílvia
author_role author
author2 Vaz, Cátia
Baptista, Cláudio
Gomes, Madalena
Gama, Adelina
Alves, Gilberto
Santos, Cecilia
Schmitt, Fernando
Socorro, Sílvia
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv uBibliorum
dc.contributor.author.fl_str_mv Marques, Ricardo
Vaz, Cátia
Baptista, Cláudio
Gomes, Madalena
Gama, Adelina
Alves, Gilberto
Santos, Cecilia
Schmitt, Fernando
Socorro, Sílvia
dc.subject.por.fl_str_mv Apoptosis
Breast cancer
Carcinogen
DMBA
Mammary gland
Regucalcin
topic Apoptosis
Breast cancer
Carcinogen
DMBA
Mammary gland
Regucalcin
description Regucalcin (RGN) is a calcium-binding protein, which has been shown to be underexpressed in cancer cases. This study aimed to determine the association of RGN expression with clinicopathological parameters of human breast cancer. In addition, the role of RGN in malignancy of mammary gland using transgenic rats overexpressing the protein (Tg-RGN) was investigated. Wild-type (Wt) and Tg-RGN rats were treated with 7,12-dimethylbenz[α]anthracene (DMBA). Carcinogen-induced tumors were histologically classified and the Ki67 proliferation index was estimated. Immunohistochemistry analysis showed that RGN immunoreactivity was negatively correlated with the histological grade of breast infiltrating ductal carcinoma suggesting that progression of breast cancer is associated with loss of RGN. Tg-RGN rats displayed lower incidence of carcinogen-induced mammary gland tumors, as well as lower incidence of invasive forms. Moreover, higher proliferation was observed in non-invasive tumors of Wt animals comparatively with Tg-RGN. Overexpression of RGN was associated with diminished expression of cell-cycle inhibitors and increased expression of apoptosis inducers. Augmented activity of apoptosis effector caspase-3 was found in the mammary gland of Tg-RGN. RGN overexpression protected from carcinogen-induced mammary gland tumor development and was linked with reduced proliferation and increased apoptosis. These findings indicated the protective role of RGN in the carcinogenesis of mammary gland.
publishDate 2015
dc.date.none.fl_str_mv 2015-01-15
2015-01-15T00:00:00Z
2019-12-04T17:00:56Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.6/7662
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.1016/j.yexcr.2014.08.007
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