Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/50549
DC FieldValueLanguage
dc.contributor.authorMarrero, María Teresaen_US
dc.contributor.authorEstévez, Saraen_US
dc.contributor.authorNegrín, Gledyen_US
dc.contributor.authorQuintana, Joseen_US
dc.contributor.authorLópez, Marianaen_US
dc.contributor.authorPérez, Francisco J.en_US
dc.contributor.authorTriana, Jorgeen_US
dc.contributor.authorLeón, Franciscoen_US
dc.contributor.authorEstévez, Franciscoen_US
dc.contributor.otherQuintana, Jose-
dc.contributor.otherEstevez, Francisco-
dc.contributor.otherLeon, Francisco-
dc.date.accessioned2018-11-24T16:54:49Z-
dc.date.available2018-11-24T16:54:49Z-
dc.date.issued2012en_US
dc.identifier.issn0006-291Xen_US
dc.identifier.urihttp://hdl.handle.net/10553/50549-
dc.description.abstractHere we demonstrate that the semi-synthetic flavonoid ayanin diacetate induces cell death selectively in leukemia cells without affecting the proliferation of normal lymphocytes. Incubation of human leukemia cells with ayanin diacetate induced G(2)-M phase cell cycle arrest and apoptosis which was prevented by the non-specific caspase inhibitor z-VAD-fmk and reduced by the overexpression of Bcl-x(L). Ayanin diacetate-induced cell death was found to be associated with: (i) loss of inner mitochondrial membrane potential, (ii) the release of cytochrome c, (iii) the activation of multiple caspases, (iv) cleavage of poly(ADP-ribose) polymerase and (v) the up-regulation of death receptors for TRAIL, DR4 and DR5. Moreover, the combined treatment with ayanin diacetate and TRAIL amplified cell death, compared to single treatments. These results provide a basis for further exploring the potential applications of this combination for the treatment of cancer.en_US
dc.languageengen_US
dc.relationEvaluación de Potenciales Compuestos Antileucémicos.en_US
dc.relation.ispartofBiochemical and biophysical research communications (Print)en_US
dc.sourceBiochemical and Biophysical Research Communications[ISSN 0006-291X],v. 428(1), p. 116-120 (Noviembre 2012)en_US
dc.subject32 Ciencias médicasen_US
dc.subject2403 Bioquímicaen_US
dc.subject.otherClinical-Implicationsen_US
dc.subject.otherInduced Apoptosisen_US
dc.subject.otherTargeting Deathen_US
dc.subject.otherDecoy Receptorsen_US
dc.subject.otherCanceren_US
dc.subject.otherP53en_US
dc.subject.otherResistanceen_US
dc.subject.otherPathwayen_US
dc.subject.otherFamilyen_US
dc.subject.otherGeneen_US
dc.titleAyanin diacetate-induced cell death is amplified by TRAIL in human leukemia cellsen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.bbrc.2012.10.017en_US
dc.identifier.scopus84868379401-
dc.identifier.isi000311523200020-
dcterms.isPartOfBiochemical And Biophysical Research Communications-
dcterms.sourceBiochemical And Biophysical Research Communications[ISSN 0006-291X],v. 428 (1), p. 116-120-
dc.contributor.authorscopusid55055343200-
dc.contributor.authorscopusid53867837200-
dc.contributor.authorscopusid36094735900-
dc.contributor.authorscopusid8681043500-
dc.contributor.authorscopusid22985994700-
dc.contributor.authorscopusid57197103237-
dc.contributor.authorscopusid55946071500-
dc.contributor.authorscopusid7005039451-
dc.contributor.authorscopusid7003810011-
dc.description.lastpage120en_US
dc.description.firstpage116en_US
dc.relation.volume428en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000311523200020-
dc.contributor.daisngid2743847-
dc.contributor.daisngid23115881-
dc.contributor.daisngid6059605-
dc.contributor.daisngid128315-
dc.contributor.daisngid5158464-
dc.contributor.daisngid34494-
dc.contributor.daisngid34895917-
dc.contributor.daisngid1400733-
dc.contributor.daisngid136703-
dc.contributor.daisngid384944-
dc.identifier.investigatorRIDK-5709-2014-
dc.identifier.investigatorRIDK-5125-2014-
dc.identifier.investigatorRIDNo ID-
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Marrero, MT-
dc.contributor.wosstandardWOS:EstevezA, S-
dc.contributor.wosstandardWOS:Negrin, G-
dc.contributor.wosstandardWOS:Quintana, J-
dc.contributor.wosstandardWOS:Lopez, M-
dc.contributor.wosstandardWOS:Perez, FJ-
dc.contributor.wosstandardWOS:Triana, J-
dc.contributor.wosstandardWOS:Leon, F-
dc.contributor.wosstandardWOS:Estevez, F-
dc.date.coverdateNoviembre 2012en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,268-
dc.description.jcr2,406-
dc.description.sjrqQ2-
dc.description.jcrqQ3-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0001-8225-4538-
crisitem.author.orcid0000-0002-9728-2774-
crisitem.author.orcid0000-0002-9728-2774-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameQuintana Aguiar, José Martín-
crisitem.author.fullNameEstévez Rosas, Francisco Jesús-
crisitem.author.fullNameEstévez Rosas, Francisco Jesús-
crisitem.project.principalinvestigatorEstévez Rosas, Francisco Jesús-
Appears in Collections:Artículos
Show simple item record

SCOPUSTM   
Citations

5
checked on Nov 24, 2024

WEB OF SCIENCETM
Citations

4
checked on Nov 24, 2024

Page view(s)

108
checked on Sep 28, 2024

Google ScholarTM

Check

Altmetric


Share



Export metadata



Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.