Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells

Detalhes bibliográficos
Autor(a) principal: Guimarães, Douglas M.
Data de Publicação: 2016
Outros Autores: Almeida, Luciana Oliveira, Martins, Manoela Domingues, Warner, Kristy, Santos-Silva, Alan Roger, Vargas, Pablo Agustin, Nunes, Fábio Daumas, Squarize, Cristiane Helena, Nor, Jacques Eduardo, Castilho, Rogerio Moraes
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/183990
Resumo: Mucoepidermoid carcinoma (MEC) is the most common malignancy of salivary glands. The response of MEC to chemotherapy is unpredictable, and recent advances in cancer biology suggest the involvement of cancer stem cells (CSCs) in tumor progression and chemoresistance and radioresistance phenotype. We found that histone acetyltransferase inhibitors (HDACi) were capable of disrupting CSCs in MEC. Furthermore, administration of HDACi prior to Cisplatin (two-hit approach) disrupts CSCs and sensitizes tumor cells to Cisplatin. Our findings corroborate to emerging evidence that CSCs play a key role in tumor resistance to chemotherapy, and highlights a pharmacological two-hit approach that disrupts tumor resistance to conventional therapy.
id UFRGS-2_f60b8df715d9326a951822d58716a00d
oai_identifier_str oai:www.lume.ufrgs.br:10183/183990
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Guimarães, Douglas M.Almeida, Luciana OliveiraMartins, Manoela DominguesWarner, KristySantos-Silva, Alan RogerVargas, Pablo AgustinNunes, Fábio DaumasSquarize, Cristiane HelenaNor, Jacques EduardoCastilho, Rogerio Moraes2018-10-26T02:43:25Z20161949-2553http://hdl.handle.net/10183/183990001059508Mucoepidermoid carcinoma (MEC) is the most common malignancy of salivary glands. The response of MEC to chemotherapy is unpredictable, and recent advances in cancer biology suggest the involvement of cancer stem cells (CSCs) in tumor progression and chemoresistance and radioresistance phenotype. We found that histone acetyltransferase inhibitors (HDACi) were capable of disrupting CSCs in MEC. Furthermore, administration of HDACi prior to Cisplatin (two-hit approach) disrupts CSCs and sensitizes tumor cells to Cisplatin. Our findings corroborate to emerging evidence that CSCs play a key role in tumor resistance to chemotherapy, and highlights a pharmacological two-hit approach that disrupts tumor resistance to conventional therapy.application/pdfengOncotarget. Albany. Vol. 7, no. 27 (July 2016), p. 42447-42460Patologia bucalCarcinoma bucalCélulas-tronco neoplásicasSensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cellsEstrangeiroinfo: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:UFRGSORIGINAL001059508.pdfTexto completo (inglês)application/pdf6047204http://www.lume.ufrgs.br/bitstream/10183/183990/1/001059508.pdff3c1eceed4e87325e850b00648b66040MD51TEXT001059508.pdf.txt001059508.pdf.txtExtracted Texttext/plain53658http://www.lume.ufrgs.br/bitstream/10183/183990/2/001059508.pdf.txta3994ce7cfcc93bd293a6076f203e496MD52THUMBNAIL001059508.pdf.jpg001059508.pdf.jpgGenerated Thumbnailimage/jpeg2269http://www.lume.ufrgs.br/bitstream/10183/183990/3/001059508.pdf.jpg1f386c8aea9d13dd8c1de85f6fea7492MD5310183/1839902018-10-27 03:12:32.192091oai:www.lume.ufrgs.br:10183/183990Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-10-27T06:12:32Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
title Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
spellingShingle Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
Guimarães, Douglas M.
Patologia bucal
Carcinoma bucal
Células-tronco neoplásicas
title_short Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
title_full Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
title_fullStr Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
title_full_unstemmed Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
title_sort Sensitizing mucoepidermoid carcinomas to chemotherapy by targeted disruption of cancer stem cells
author Guimarães, Douglas M.
author_facet Guimarães, Douglas M.
Almeida, Luciana Oliveira
Martins, Manoela Domingues
Warner, Kristy
Santos-Silva, Alan Roger
Vargas, Pablo Agustin
Nunes, Fábio Daumas
Squarize, Cristiane Helena
Nor, Jacques Eduardo
Castilho, Rogerio Moraes
author_role author
author2 Almeida, Luciana Oliveira
Martins, Manoela Domingues
Warner, Kristy
Santos-Silva, Alan Roger
Vargas, Pablo Agustin
Nunes, Fábio Daumas
Squarize, Cristiane Helena
Nor, Jacques Eduardo
Castilho, Rogerio Moraes
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Guimarães, Douglas M.
Almeida, Luciana Oliveira
Martins, Manoela Domingues
Warner, Kristy
Santos-Silva, Alan Roger
Vargas, Pablo Agustin
Nunes, Fábio Daumas
Squarize, Cristiane Helena
Nor, Jacques Eduardo
Castilho, Rogerio Moraes
dc.subject.por.fl_str_mv Patologia bucal
Carcinoma bucal
Células-tronco neoplásicas
topic Patologia bucal
Carcinoma bucal
Células-tronco neoplásicas
description Mucoepidermoid carcinoma (MEC) is the most common malignancy of salivary glands. The response of MEC to chemotherapy is unpredictable, and recent advances in cancer biology suggest the involvement of cancer stem cells (CSCs) in tumor progression and chemoresistance and radioresistance phenotype. We found that histone acetyltransferase inhibitors (HDACi) were capable of disrupting CSCs in MEC. Furthermore, administration of HDACi prior to Cisplatin (two-hit approach) disrupts CSCs and sensitizes tumor cells to Cisplatin. Our findings corroborate to emerging evidence that CSCs play a key role in tumor resistance to chemotherapy, and highlights a pharmacological two-hit approach that disrupts tumor resistance to conventional therapy.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2018-10-26T02:43:25Z
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/10183/183990
dc.identifier.issn.pt_BR.fl_str_mv 1949-2553
dc.identifier.nrb.pt_BR.fl_str_mv 001059508
identifier_str_mv 1949-2553
001059508
url http://hdl.handle.net/10183/183990
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Oncotarget. Albany. Vol. 7, no. 27 (July 2016), p. 42447-42460
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/10183/183990/1/001059508.pdf
http://www.lume.ufrgs.br/bitstream/10183/183990/2/001059508.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/183990/3/001059508.pdf.jpg
bitstream.checksum.fl_str_mv f3c1eceed4e87325e850b00648b66040
a3994ce7cfcc93bd293a6076f203e496
1f386c8aea9d13dd8c1de85f6fea7492
bitstream.checksumAlgorithm.fl_str_mv MD5
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_ 1801224954278051840