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dc.contributor.authorDíaz Rodríguez, María Elena 
dc.contributor.authorHernández-García, Susana
dc.contributor.authorSanz, Eduardo
dc.contributor.authorPandiella Alonso, Atanasio 
dc.date.accessioned2026-04-14T14:45:24Z
dc.date.available2026-04-14T14:45:24Z
dc.date.issued2016-02-02
dc.identifier.citationDíaz-Rodríguez, E., Hernández-García, S., Sanz, E., & Pandiella, A. (2016). Antitumoral effect of Ocoxin on acute myeloid leukemia. Oncotarget, 7(5), 6231-6242. https://doi.org/10.18632/ONCOTARGET.6862. PMID: 26756220; PMCID: PMC4868752.es_ES
dc.identifier.urihttp://hdl.handle.net/10366/170984
dc.description.abstract[EN]Acute myeloid leukemia (AML) is a heterogeneous hematological malignancy whose incidence is growing in developed countries. In the relapse setting, very limited therapeutic options are available and in most cases only palliative care can be offered to patients. The effect of a composite formulation that contains several antioxidants, Ocoxin Oral solution (OOS), was tested in this condition. When analyzed in vitro, OOS exhibited anti-AML action that was both time and dose dependent. In vivo OOS induced a ralentization of tumor growth that was due to a decrease in cell proliferation. Such effect could, at least partially, be due to an increase in the cell cycle inhibitor p27, although other cell cycle proteins seemed to be altered. Besides, OOS induced an immunomodulatory effect through the induction of IL6. When tested in combination with other therapeutic agents normally used in the treatment of AML patients, OOS demonstrated a higher antiproliferative action, suggesting that it may be used in combination with those standard of care treatments to potentiate their antiproliferative action in the AML clinic.es_ES
dc.language.isoenges_ES
dc.publisherImpact Journalses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacionales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/es_ES
dc.subjectAcute myeloid leukemiaes_ES
dc.subjectAntioxidantses_ES
dc.subjectCell cyclees_ES
dc.subjectp27es_ES
dc.subject.meshAntioxidants *
dc.subject.meshZinc Sulfate *
dc.subject.meshAscorbic Acid *
dc.subject.meshLeukemia *
dc.subject.meshCell Cycle *
dc.subject.meshPlant Extracts *
dc.subject.meshXenograft Model Antitumor Assays *
dc.subject.meshHumans *
dc.subject.meshVitamin B 6 *
dc.subject.meshCell Line *
dc.subject.meshCell Proliferation *
dc.subject.meshFolic Acid *
dc.subject.meshRandom Allocation *
dc.subject.meshApoptosis *
dc.subject.meshPantothenic Acid *
dc.subject.meshVitamin B 12 *
dc.subject.meshAnimals *
dc.subject.meshMice *
dc.titleAntitumoral effect of ocoxin on acute myeloid leukemiaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.18632/ONCOTARGET.6862es_ES
dc.subject.unesco2302es_ES
dc.subject.unesco3207.08 Hematologíaes_ES
dc.identifier.doi10.18632/oncotarget.6862
dc.relation.projectIDFU2012-39151es_ES
dc.relation.projectIDAECCes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid26756220
dc.identifier.essn1949-2553
dc.journal.titleOncotargetes_ES
dc.volume.number7es_ES
dc.issue.number5es_ES
dc.page.initial6231es_ES
dc.page.final6242es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsácido pantoténico *
dc.subject.decsapoptosis *
dc.subject.decshumanos *
dc.subject.decsratones *
dc.subject.decslínea celular *
dc.subject.decsdistribución aleatoria *
dc.subject.decsleucemia *
dc.subject.decsvitamina B 6 *
dc.subject.decsextractos de plantas *
dc.subject.decsácido fólico *
dc.subject.decsensayos antitumorales por modelo de xenoinjerto *
dc.subject.decsanimales *
dc.subject.decsácido ascórbico *
dc.subject.decsciclo celular *
dc.subject.decsvitamina B 12 *
dc.subject.decsantioxidantes *
dc.subject.decssulfato de zinc *
dc.subject.decsproliferación celular *


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