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dc.creatorLeón González, Antonio Josées
dc.creatorSáez Martínez, Prudencioes
dc.creatorJiménez Vacas, Juan M.es
dc.creatorHerrero Aguayo, Vicentees
dc.creatorMontero Hidalgo, Antonio J.es
dc.creatorGómez Gómez, Enriquees
dc.creatorMadrona, Andréses
dc.creatorCastaño, Justo P.es
dc.creatorEspartero Sánchez, José Luises
dc.creatorGahete, Manuel D.es
dc.creatorLuque, Raúl M.es
dc.date.accessioned2021-09-10T16:36:14Z
dc.date.available2021-09-10T16:36:14Z
dc.date.issued2021
dc.identifier.citationLeón González, A.J., Sáez Martínez, P., Jiménez Vacas, J.M., Herrero Aguayo, V., Montero Hidalgo, A.J., Gómez Gómez, E.,...,Luque, R.M. (2021). Comparative cytotoxic activity of hydroxytyrosol and its semisynthetic lipophilic derivatives in prostate cancer cells. Antioxidants, 10 (9), 1348.
dc.identifier.issn2076-3921es
dc.identifier.urihttps://hdl.handle.net/11441/125626
dc.description.abstractA high adherence to a Mediterranean diet has been related to numerous beneficial effects in human health, including a lower incidence and mortality of prostate cancer (PCa). Olive oil is an important source of phenolic bioactive compounds, mainly hydroxytyrosol (HT), of this diet. Be-cause of the growing interest of this compound and its derivatives as a cancer chemopreventive agent, we aimed to compare the in vitro effect of HT isolated from olive mill wastewaters and five semisynthetic alkyl ether, ester, and nitro-derivatives against prostate cancer (PCa) cell lines. The effect in cell proliferation was determined in RWPE-1, LNCaP, 22Rv1, and PC-3 cells by resazurin assay, the effect in cell migration by wound healing assay, and tumorsphere and colony formation were evaluated. The changes in key signaling pathways involved in carcinogenesis were assessed by using a phosphorylation pathway profiling array and by Western blotting. Antiproliferative effects of HT and two lipophilic derivatives [hydroxytyrosyl acetate (HT-Ac)/ethyl hydroxytyrosyl ether (HT-Et)] were significantly higher in cancerous PC-3 and 22Rv1 cells than in non-malignant RWPE-1 cells. HT/HT-Ac/HT-Et significantly reduced migration capacity in RWPE-1 and PC-3 and prostatosphere size and colony formation in 22Rv1, whereas only HT-Ac and HT-Et reduced these functional parameters in PC-3. The cytotoxic effect in 22Rv1 cells was correlated with modifications in the phosphorylation pattern of key proteins, including ERK1/2 and AKT. Consistently, HT-Ac and HT-Et decreased p-AKT levels in PC-3. In sum, our results suggest that HT and its lipophilic derivatives could be considered as potential therapeutic tools in PCa.es
dc.description.sponsorshipJunta de Andalucía PI-0152-2019, BIO-0139, RH-0084-2020es
dc.description.sponsorshipMinisterio de Economía y Competitividad PID2019-105564RB-I00, PID2019-105201RB-I00, FPU17/00263, FPU16/06190, FPU18/02485es
dc.formatapplication/pdfes
dc.format.extent16 p.es
dc.language.isoenges
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)es
dc.relation.ispartofAntioxidants, 10 (9), 1348-.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAnticanceres
dc.subjectExtra virgin olive oiles
dc.subjectHydroxytyrosoles
dc.subjectProstate canceres
dc.subjectSemisynthetic derivativeses
dc.titleComparative cytotoxic activity of hydroxytyrosol and its semisynthetic lipophilic derivatives in prostate cancer cellses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química Orgánica y Farmacéuticaes
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Farmacologíaes
dc.relation.projectIDPI-0152-2019es
dc.relation.projectIDBIO-0139es
dc.relation.projectIDRH-0084-2020es
dc.relation.projectIDPID2019-105564RB-I00es
dc.relation.projectIDPID2019-105201RB-100es
dc.relation.projectIDFPU17/00263es
dc.relation.projectIDFPU16/06190es
dc.relation.projectIDFPU18/02485es
dc.relation.publisherversionhttps://doi.org/10.3390/antiox10091348es
dc.identifier.doi10.3390/antiox10091348es
dc.journaltitleAntioxidantses
dc.publication.volumen10es
dc.publication.issue9es
dc.publication.initialPage1348es
dc.description.awardwinningPremio Mensual Publicación Científica Destacada de la US. Facultad de Farmacia

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