Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line

Detalhes bibliográficos
Autor(a) principal: Freitas, Mariana
Data de Publicação: 2011
Outros Autores: Alves, Vera, Sarmento-Ribeiro, Ana Bela, Mota-Pinto, Anabela
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/20321
https://doi.org/10.1016/j.bbrc.2011.04.109
Resumo: Docetaxel and sodium selenite are well known for their anticancer properties. While resistance to docetaxel remains an obstacle in prostate cancer chemotherapy, sodium selenite, has been exploited as a new therapeutic approach. Currently, development of therapies affecting a multitude of cell targets, have been proposed as a strategy to overcome drug resistance. This association may reduce systemic toxicity counteracting a wide range of side effects. Here we report the effect of docetaxel and sodium selenite combination on the PC3 prostate cancer cell line, derived from bone metastasis. Therefore we evaluate cell growth, cell cycle progression, viability, mitochondria membrane potential, cytochrome C, Bax/Bcl2 ratio, caspase-3 expression and reactive oxygen species production. Our results suggest that sodium selenite and docetaxel combination have a synergistic effect on cell growth inhibition (67%) compared with docetaxel (22%) and sodium selenite (24%) alone. This combination also significantly induced cell death, mainly by late apoptosis vs necrosis, which is correlated with mitochondria membrane potential depletion. On the other hand, cytochrome C, Bax/Bcl2 ratio and caspase-3, known as proapoptotic factors, significantly increased in the presence of sodium selenite alone, but not in the presence of docetaxel in monotherapy or in combination with sodium selenite. These findings suggest that docetaxel and sodium selenite combination may be more effective on prostate cancer treatment than docetaxel alone warranting further evaluation of this combination in prostate cancer therapeutic approach.
id RCAP_7a3b4b6f3953aa82e7ea6a35d1161ccc
oai_identifier_str oai:estudogeral.uc.pt:10316/20321
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell lineProstate cancerDocetaxelSodium seleniteSynergistic effectChemotherapyDocetaxel and sodium selenite are well known for their anticancer properties. While resistance to docetaxel remains an obstacle in prostate cancer chemotherapy, sodium selenite, has been exploited as a new therapeutic approach. Currently, development of therapies affecting a multitude of cell targets, have been proposed as a strategy to overcome drug resistance. This association may reduce systemic toxicity counteracting a wide range of side effects. Here we report the effect of docetaxel and sodium selenite combination on the PC3 prostate cancer cell line, derived from bone metastasis. Therefore we evaluate cell growth, cell cycle progression, viability, mitochondria membrane potential, cytochrome C, Bax/Bcl2 ratio, caspase-3 expression and reactive oxygen species production. Our results suggest that sodium selenite and docetaxel combination have a synergistic effect on cell growth inhibition (67%) compared with docetaxel (22%) and sodium selenite (24%) alone. This combination also significantly induced cell death, mainly by late apoptosis vs necrosis, which is correlated with mitochondria membrane potential depletion. On the other hand, cytochrome C, Bax/Bcl2 ratio and caspase-3, known as proapoptotic factors, significantly increased in the presence of sodium selenite alone, but not in the presence of docetaxel in monotherapy or in combination with sodium selenite. These findings suggest that docetaxel and sodium selenite combination may be more effective on prostate cancer treatment than docetaxel alone warranting further evaluation of this combination in prostate cancer therapeutic approach.2011-04-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/20321http://hdl.handle.net/10316/20321https://doi.org/10.1016/j.bbrc.2011.04.109enghttp://www.sciencedirect.com/science/article/pii/S0006291X11007078Freitas, MarianaAlves, VeraSarmento-Ribeiro, Ana BelaMota-Pinto, Anabelainfo: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:RCAAP2022-05-25T05:50:32Zoai:estudogeral.uc.pt:10316/20321Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:39.448685Repositório 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 Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
title Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
spellingShingle Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
Freitas, Mariana
Prostate cancer
Docetaxel
Sodium selenite
Synergistic effect
Chemotherapy
title_short Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
title_full Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
title_fullStr Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
title_full_unstemmed Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
title_sort Combined effect of sodium selenite and docetaxel on PC3 metastatic prostate cancer cell line
author Freitas, Mariana
author_facet Freitas, Mariana
Alves, Vera
Sarmento-Ribeiro, Ana Bela
Mota-Pinto, Anabela
author_role author
author2 Alves, Vera
Sarmento-Ribeiro, Ana Bela
Mota-Pinto, Anabela
author2_role author
author
author
dc.contributor.author.fl_str_mv Freitas, Mariana
Alves, Vera
Sarmento-Ribeiro, Ana Bela
Mota-Pinto, Anabela
dc.subject.por.fl_str_mv Prostate cancer
Docetaxel
Sodium selenite
Synergistic effect
Chemotherapy
topic Prostate cancer
Docetaxel
Sodium selenite
Synergistic effect
Chemotherapy
description Docetaxel and sodium selenite are well known for their anticancer properties. While resistance to docetaxel remains an obstacle in prostate cancer chemotherapy, sodium selenite, has been exploited as a new therapeutic approach. Currently, development of therapies affecting a multitude of cell targets, have been proposed as a strategy to overcome drug resistance. This association may reduce systemic toxicity counteracting a wide range of side effects. Here we report the effect of docetaxel and sodium selenite combination on the PC3 prostate cancer cell line, derived from bone metastasis. Therefore we evaluate cell growth, cell cycle progression, viability, mitochondria membrane potential, cytochrome C, Bax/Bcl2 ratio, caspase-3 expression and reactive oxygen species production. Our results suggest that sodium selenite and docetaxel combination have a synergistic effect on cell growth inhibition (67%) compared with docetaxel (22%) and sodium selenite (24%) alone. This combination also significantly induced cell death, mainly by late apoptosis vs necrosis, which is correlated with mitochondria membrane potential depletion. On the other hand, cytochrome C, Bax/Bcl2 ratio and caspase-3, known as proapoptotic factors, significantly increased in the presence of sodium selenite alone, but not in the presence of docetaxel in monotherapy or in combination with sodium selenite. These findings suggest that docetaxel and sodium selenite combination may be more effective on prostate cancer treatment than docetaxel alone warranting further evaluation of this combination in prostate cancer therapeutic approach.
publishDate 2011
dc.date.none.fl_str_mv 2011-04-28
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/20321
http://hdl.handle.net/10316/20321
https://doi.org/10.1016/j.bbrc.2011.04.109
url http://hdl.handle.net/10316/20321
https://doi.org/10.1016/j.bbrc.2011.04.109
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://www.sciencedirect.com/science/article/pii/S0006291X11007078
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799133708553289728