Utilize este identificador para referenciar este registo:
https://hdl.handle.net/10316/109644
Campo DC | Valor | Idioma |
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dc.contributor.author | Oliveira, José Miguel P. Ferreira de | - |
dc.contributor.author | Costa, Maria | - |
dc.contributor.author | Pedrosa, Tiago | - |
dc.contributor.author | Pinto, Pedro | - |
dc.contributor.author | Remédios, Catarina | - |
dc.contributor.author | Oliveira, Helena | - |
dc.contributor.author | Pimentel, Francisco | - |
dc.contributor.author | Almeida, Luís | - |
dc.contributor.author | Santos, Conceição | - |
dc.date.accessioned | 2023-10-19T10:36:16Z | - |
dc.date.available | 2023-10-19T10:36:16Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | https://hdl.handle.net/10316/109644 | - |
dc.description.abstract | Sulforaphane (SFN) is a naturally-occurring isothiocyanate best known for its role as an indirect antioxidant. Notwithstanding, in different cancer cell lines, SFN may promote the accumulation of reactive oxygen species (ROS) and cause cell death e.g. by apoptosis. Osteosarcoma often becomes chemoresistant, and new molecular targets to prevent drug resistance are needed. Here, we aimed to determine the effect of SFN on ROS levels and to identify key biomarkers leading to ROS unbalance and apoptosis in the p53-null MG-63 osteosarcoma cell line. MG-63 cells were exposed to SFN for up to 48 h. At 10 μM concentration or higher, SFN decreased cell viability, increased the%early apoptotic cells and increased caspase 3 activity. At these higher doses, SFN increased ROS levels, which correlated with apoptotic endpoints and cell viability decline. In exposed cells, gene expression analysis revealed only partial induction of phase-2 detoxification genes. More importantly, SFN inhibited ROS-scavenging enzymes and impaired glutathione recycling, as evidenced by inhibition of glutathione reductase (GR) activity and combined inhibition of glutathione peroxidase (GPx) gene expression and enzyme activity. In conclusion, SFN induced oxidative stress and apoptosis via a p53-independent mechanism. GPx expression and activity were found associated with ROS accumulation in MG-63 cells and are potential biomarkers for the efficacy of ROS-inducing agents e.g. as co-adjuvant drugs in osteosarcoma. | pt |
dc.language.iso | eng | pt |
dc.publisher | Public Library of Science | pt |
dc.relation | SFRH/BPD/48853/2008 | pt |
dc.relation | SFRH/BPD/74868/2010 | pt |
dc.rights | openAccess | pt |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt |
dc.title | Sulforaphane induces oxidative stress and death by p53-independent mechanism: implication of impaired glutathione recycling | pt |
dc.type | article | pt |
degois.publication.firstPage | e92980 | pt |
degois.publication.issue | 3 | pt |
degois.publication.title | PLoS ONE | pt |
dc.peerreviewed | yes | pt |
dc.identifier.doi | 10.1371/journal.pone.0092980 | - |
degois.publication.volume | 9 | pt |
dc.date.embargo | 2014-01-01 | * |
dc.identifier.pmid | 24667842 | - |
uc.date.periodoEmbargo | 0 | pt |
dc.identifier.eissn | 1932-6203 | - |
item.openairetype | article | - |
item.fulltext | Com Texto completo | - |
item.languageiso639-1 | en | - |
item.grantfulltext | open | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.researchunit | CEISUC - Center for Health Studies and Research of the University of Coimbra | - |
crisitem.author.orcid | 0000-0001-5993-5132 | - |
Aparece nas coleções: | I&D CEISUC - Artigos em Revistas Internacionais |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
---|---|---|---|---|
Sulforaphane-induces-oxidative-stress-and-death-by-p53independent-mechanism-Implication-of-impaired-glutathione-recyclingPLoS-ONE.pdf | 683.31 kB | Adobe PDF | Ver/Abrir |
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