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dc.contributor.authorMartín, Rubén-
dc.contributor.authorIbeas, Elvira-
dc.contributor.authorCarvalho-Tavares, Juliana-
dc.contributor.authorHernández, Marita-
dc.contributor.authorRuiz-Gutiérrez, Valentina-
dc.contributor.authorNieto, María Luisa-
dc.date.accessioned2009-07-01T10:48:06Z-
dc.date.available2009-07-01T10:48:06Z-
dc.date.issued2009-06-22-
dc.identifier.citationPLoS ONE 4(6): e5975 (2009)en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/10261/14147-
dc.description.abstract[Background]: Triterpene alcohols and acids are multifunctional compounds widely distributed throughout the plant kingdom that exhibit a variety of beneficial health properties, being synthetic analogs of oleanolic acid under clinical evaluation as anti-tumoral therapeutic agents. However, the antineoplastic activity of two natural occuring triterpenoid alcohols extracted from olive oil, erythrodiol (an intermediate from oleanolic acid), and its isomer, uvaol, has barely been reported, particularly on brain cancer cells. Astrocytomas are among the most common and aggressive type of primary malignant tumors in the neurological system lacking effective treatments, and in this study, we addressed the effect of these two triterpenic diols on the human 1321N1 astrocytoma cell line.en_US
dc.description.abstract[Principal Findings]: Erythrodiol and uvaol effectively affected cell proliferation, as well as cell cycle phases and induced 1321N1 cell death. Both triterpenes successfully modulated the apoptotic response, promoting nuclear condensation and fragmentation. They caused retraction and rounding of cultured cells, which lost adherence from their supports, while F-actin and vimentin filaments disappeared as an organized cytoplasmic network. At molecular level, changes in the expression of surface proteins associated with adhesion or death processes were also observed. Moreover, triterpene exposure resulted in the production of reactive oxygen species (ROS) with loss of mitochondrial transmembrane potential, and correlated with the activation of c-Jun N-terminal kinases (JNK). The presence of catalase reversed the triterpenic diols-induced mitochondrial depolarization, JNK activation, and apoptotic death, indicating the critical role of ROS in the action of these compounds.en_US
dc.description.abstract[Conclusions]: Overall, we provide a significant insight into the anticarcinogenic action of erythrodiol and uvaol that may have a potential in prevention and treatment of brain tumors and other cancers.en_US
dc.description.sponsorshipThis study has been funded by a grants SAF2005-01242, SAF2008-00245 and AGL2008-022845 from MICINN, and CSI11A08 from the Government of Castilla y Leon. MH is under the Ramon y Cajal Program (Co-funded by F.S.E.). E.I., R.M. and J.C-T. are supported by a fellowship from the Spanish Ministerio de Educación y Ciencia.en_US
dc.format.extent877431 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofPublisher's version-
dc.rightsopenAccessen_US
dc.subjectTriterpenicen_US
dc.subjectJNKen_US
dc.subjectROSen_US
dc.subjectAstrocytomasen_US
dc.titleNatural triterpenic diols promote apoptosis in astrocytoma cells through ROS-mediated mitochondrial depolarization and JNK activationen_US
dc.typeartículoen_US
dc.identifier.doi10.1371/journal.pone.0005975-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1371/journal.pone.0005975-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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