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dc.contributor.authorDíaz Rodríguez, María Elena 
dc.contributor.authorEl-Mallah, Al-Mahy
dc.contributor.authorSanz, Eduardo
dc.contributor.authorPandiella Alonso, Atanasio 
dc.date.accessioned2026-04-10T10:03:06Z
dc.date.available2026-04-10T10:03:06Z
dc.date.issued2017-08
dc.identifier.citationDíaz-Rodríguez, E., El-Mallah, A.-M., Sanz, E., & Pandiella, A. (2017). Antitumoral effect of ocoxin in hepatocellular carcinoma. Oncology Letters, 14(2), 1950-1958. https://doi.org/10.3892/OL.2017.64400. Epub 2017 Jun 21. PMID: 28781639; PMCID: PMC5530179.es_ES
dc.identifier.issn1792-1074
dc.identifier.urihttp://hdl.handle.net/10366/170913
dc.description.abstract[EN]Hepatocellular carcinoma (HCC) is becoming one of the most prevalent types of cancer worldwide. The most efficient types of treatment at present include surgical resection and liver transplantation, but these treatments may only be used in a small percentage of patients. In order to identify novel therapeutic strategies for this disease, the present study explored the potential antitumoral effect of Ocoxin® oral solution (OOS) in HCC. OOS inhibited the proliferation of HCC cell lines in a time- and dose-dependent manner, being more efficient when used in combination with sorafenib, a standard of care treatment for patients diagnosed with advanced-stage disease. Mechanistic studies indicated that the effect of OOS was due to the induction of cell cycle arrest rather than the stimulation of apoptotic cell death. The cell cycle was slowed down in all phases in the HCC cell lines treated with OOS. Finally, when tested in animal models of HCC, OOS reduced tumor progression through the induction of necrosis in xenograft tumor models. Considering the poor prognosis and high resistance to antitumor treatments of HCC, the antiproliferative action of OOS, particularly in combination with sorafenib, provides the opportunity to investigate the effect of combined therapy in a clinical setting.es_ES
dc.language.isoenges_ES
dc.publisherSpandidos Publicationses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacionales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/es_ES
dc.subjectAntioxidantses_ES
dc.subjectCell cyclees_ES
dc.subjectHepatocellular carcinomaes_ES
dc.subject.meshAntioxidants *
dc.subject.meshCarcinoma, Hepatocellular *
dc.subject.meshCell Cycle *
dc.titleAntitumoral effect of ocoxin in hepatocellular carcinomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3892/OL.2017.6440es_ES
dc.subject.unesco2302 Bioquímicaes_ES
dc.subject.unesco3207.13 Oncologíaes_ES
dc.identifier.doi10.3892/ol.2017.6440
dc.relation.projectIDBFU2012-39151es_ES
dc.relation.projectIDAECC12/GC02es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.identifier.pmid28781639
dc.journal.titleOncology Letterses_ES
dc.volume.number14es_ES
dc.issue.number2es_ES
dc.page.initial1950es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsciclo celular *
dc.subject.decsantioxidantes *
dc.subject.decscarcinoma hepatocelular *


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 Internacional