In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma
Autor(a) principal: | |
---|---|
Data de Publicação: | 2014 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/179263 |
Resumo: | Histone deacetylase inhibitors and bisphosphonates have a promising future in the treatment of cancer as targeted anticancer drugs, particularly when used together or in combination with other cytotoxic agents. However, the effects of these combined treatments have not yet been systematically evaluated in Ewing sarcoma. The in vitro effects on cellular proliferation, viability and survival were investigated in two Ewing sarcoma cell lines, SK-ES-1 and RD-ES. The cell lines were treated with sodium butyrate, a histone deacetylase inhibitor and zoledronic acid, a bisphosphonate, alone, together or in combination with chemotherapeutic drugs recommended for clinical treatment of Ewing sarcoma. The data demonstrated that the combination of sodium butyrate and zoledronic acid had a synergistic cytotoxic effect at 72 h following treatment, persisting for 10-14 days post-treatment, in both cell lines tested. All combinations between sodium butyrate or zoledronic acid and the traditional antineoplastic drugs (doxorubicin, etoposide and vincristine) demonstrated a synergistic cytotoxic effect at 72 h in SK-ES-1 and RD-ES cells, except for the combinations of sodium butyrate with vincristine and of zoledronic acid with doxorubicin, which showed only an additive effect in RD-ES cell lines as compared to each agent alone. These acute effects observed in both Ewing sarcoma cell lines were confirmed by the clonogenic assay. The present data suggest that combining histone deacetylase inhibitors and bisphosphonates with traditional chemotherapeutic drugs is a promising therapeutic strategy for the treatment of Ewing sarcoma, and provides a basis for further studies in this field. |
id |
UFRGS-2_716e4f9b66e12c553209447cc63e8120 |
---|---|
oai_identifier_str |
oai:www.lume.ufrgs.br:10183/179263 |
network_acronym_str |
UFRGS-2 |
network_name_str |
Repositório Institucional da UFRGS |
repository_id_str |
|
spelling |
Santos, Michel Pinheiro dosFarias, Caroline Brunetto deRoesler, RafaelBrunetto, Algemir LunardiAbujamra, Ana Lúcia2018-06-09T03:34:51Z20141021-335Xhttp://hdl.handle.net/10183/179263001068630Histone deacetylase inhibitors and bisphosphonates have a promising future in the treatment of cancer as targeted anticancer drugs, particularly when used together or in combination with other cytotoxic agents. However, the effects of these combined treatments have not yet been systematically evaluated in Ewing sarcoma. The in vitro effects on cellular proliferation, viability and survival were investigated in two Ewing sarcoma cell lines, SK-ES-1 and RD-ES. The cell lines were treated with sodium butyrate, a histone deacetylase inhibitor and zoledronic acid, a bisphosphonate, alone, together or in combination with chemotherapeutic drugs recommended for clinical treatment of Ewing sarcoma. The data demonstrated that the combination of sodium butyrate and zoledronic acid had a synergistic cytotoxic effect at 72 h following treatment, persisting for 10-14 days post-treatment, in both cell lines tested. All combinations between sodium butyrate or zoledronic acid and the traditional antineoplastic drugs (doxorubicin, etoposide and vincristine) demonstrated a synergistic cytotoxic effect at 72 h in SK-ES-1 and RD-ES cells, except for the combinations of sodium butyrate with vincristine and of zoledronic acid with doxorubicin, which showed only an additive effect in RD-ES cell lines as compared to each agent alone. These acute effects observed in both Ewing sarcoma cell lines were confirmed by the clonogenic assay. The present data suggest that combining histone deacetylase inhibitors and bisphosphonates with traditional chemotherapeutic drugs is a promising therapeutic strategy for the treatment of Ewing sarcoma, and provides a basis for further studies in this field.application/pdfengOncology reports. Athens. Vol. 31, no. 2 (Feb. 2014), p. 955-968Sarcoma de EwingÁcido butíricoDifosfonatosQuimioterapia adjuvanteIn vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcomaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001068630.pdf001068630.pdfTexto completo (inglês)application/pdf1097055http://www.lume.ufrgs.br/bitstream/10183/179263/1/001068630.pdfaba87dad35648169e42275b7eeb6f93fMD51TEXT001068630.pdf.txt001068630.pdf.txtExtracted Texttext/plain65399http://www.lume.ufrgs.br/bitstream/10183/179263/2/001068630.pdf.txtce85db61878354e57a3f2c7ef4d69140MD5210183/1792632018-06-10 02:35:41.948951oai:www.lume.ufrgs.br:10183/179263Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-06-10T05:35:41Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
title |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
spellingShingle |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma Santos, Michel Pinheiro dos Sarcoma de Ewing Ácido butírico Difosfonatos Quimioterapia adjuvante |
title_short |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
title_full |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
title_fullStr |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
title_full_unstemmed |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
title_sort |
In vitro antitumor effect of sodium butyrate and zoledronic acid combined with traditional chemotherapeutic drugs : a paradigm of synergistic molecular targeting in the treatment of Ewing sarcoma |
author |
Santos, Michel Pinheiro dos |
author_facet |
Santos, Michel Pinheiro dos Farias, Caroline Brunetto de Roesler, Rafael Brunetto, Algemir Lunardi Abujamra, Ana Lúcia |
author_role |
author |
author2 |
Farias, Caroline Brunetto de Roesler, Rafael Brunetto, Algemir Lunardi Abujamra, Ana Lúcia |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santos, Michel Pinheiro dos Farias, Caroline Brunetto de Roesler, Rafael Brunetto, Algemir Lunardi Abujamra, Ana Lúcia |
dc.subject.por.fl_str_mv |
Sarcoma de Ewing Ácido butírico Difosfonatos Quimioterapia adjuvante |
topic |
Sarcoma de Ewing Ácido butírico Difosfonatos Quimioterapia adjuvante |
description |
Histone deacetylase inhibitors and bisphosphonates have a promising future in the treatment of cancer as targeted anticancer drugs, particularly when used together or in combination with other cytotoxic agents. However, the effects of these combined treatments have not yet been systematically evaluated in Ewing sarcoma. The in vitro effects on cellular proliferation, viability and survival were investigated in two Ewing sarcoma cell lines, SK-ES-1 and RD-ES. The cell lines were treated with sodium butyrate, a histone deacetylase inhibitor and zoledronic acid, a bisphosphonate, alone, together or in combination with chemotherapeutic drugs recommended for clinical treatment of Ewing sarcoma. The data demonstrated that the combination of sodium butyrate and zoledronic acid had a synergistic cytotoxic effect at 72 h following treatment, persisting for 10-14 days post-treatment, in both cell lines tested. All combinations between sodium butyrate or zoledronic acid and the traditional antineoplastic drugs (doxorubicin, etoposide and vincristine) demonstrated a synergistic cytotoxic effect at 72 h in SK-ES-1 and RD-ES cells, except for the combinations of sodium butyrate with vincristine and of zoledronic acid with doxorubicin, which showed only an additive effect in RD-ES cell lines as compared to each agent alone. These acute effects observed in both Ewing sarcoma cell lines were confirmed by the clonogenic assay. The present data suggest that combining histone deacetylase inhibitors and bisphosphonates with traditional chemotherapeutic drugs is a promising therapeutic strategy for the treatment of Ewing sarcoma, and provides a basis for further studies in this field. |
publishDate |
2014 |
dc.date.issued.fl_str_mv |
2014 |
dc.date.accessioned.fl_str_mv |
2018-06-09T03:34:51Z |
dc.type.driver.fl_str_mv |
Estrangeiro 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://hdl.handle.net/10183/179263 |
dc.identifier.issn.pt_BR.fl_str_mv |
1021-335X |
dc.identifier.nrb.pt_BR.fl_str_mv |
001068630 |
identifier_str_mv |
1021-335X 001068630 |
url |
http://hdl.handle.net/10183/179263 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Oncology reports. Athens. Vol. 31, no. 2 (Feb. 2014), p. 955-968 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRGS instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
instname_str |
Universidade Federal do Rio Grande do Sul (UFRGS) |
instacron_str |
UFRGS |
institution |
UFRGS |
reponame_str |
Repositório Institucional da UFRGS |
collection |
Repositório Institucional da UFRGS |
bitstream.url.fl_str_mv |
http://www.lume.ufrgs.br/bitstream/10183/179263/1/001068630.pdf http://www.lume.ufrgs.br/bitstream/10183/179263/2/001068630.pdf.txt |
bitstream.checksum.fl_str_mv |
aba87dad35648169e42275b7eeb6f93f ce85db61878354e57a3f2c7ef4d69140 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS) |
repository.mail.fl_str_mv |
|
_version_ |
1815447662550319104 |