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dc.contributor.authorLaborda-Illanes, Auroraes_ES
dc.contributor.authorSánchez-Alcoholado, Lidiaes_ES
dc.contributor.authorCastellano-Castillo, Danieles_ES
dc.contributor.authorBoutriq, Soukainaes_ES
dc.contributor.authorPlaza-Andrades, Isaaces_ES
dc.contributor.authorAranega-Martín, Lucíaes_ES
dc.contributor.authorPeralta-Linero, Jesúses_ES
dc.contributor.authorAlba, Emilioes_ES
dc.contributor.authorGonzález González, Aliciaes_ES
dc.contributor.authorQueipo-Ortuño, María Isabeles_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-01-16T15:36:36Z
dc.date.available2023-01-16T15:36:36Z
dc.date.issued2023es_ES
dc.identifier.issn0753-3322es_ES
dc.identifier.issn1950-6007es_ES
dc.identifier.urihttps://hdl.handle.net/10902/27217
dc.description.abstractMelatonin is a molecule with different antitumor actions in breast cancer and has been described as an inhibitor of vascular endothelial growth factor (VEGF). Despite the recognition of the key role exerted by VEGF in tumor angiogenesis, limitations arise when developing models to test new antiangiogenic molecules. Thus, the aim of this study was to develop rapid, economic, high capacity and easy handling angiogenesis assays to test the antiangiogenic effects of melatonin and demonstrate its most effective dose to neutralize and interfere with the angiogenic sprouting effect induced by VEGF and MCF-7. To perform this, 3D endothelial cell (HUVEC) spheroids and a chicken embryo chorioallantoic membrane (CAM) assay were used. The results showed that VEGF and MCF-7 were able to stimulate the sprouting of the new vessels in 3D endothelial spheroids and the CAM assay, and that melatonin had an inhibitory effect on angiogenesis. Specifically, as the 1 mM pharmacological dose was the only effective dose able to inhibit the formation of ramifications around the alginate in the CAM assay model, this inhibition was shown to occur in a dose-dependent manner. Taken together, these techniques represent novel tools for the development of antiangiogenic molecules such as melatonin, with possible implications for the therapy of breast cancer.es_ES
dc.description.sponsorshipFunding: This work was funded in part by PE-0106–2019 from the Consejería de Salud de la Junta de Andalucía, C19047–2018 from Fundación Unicaja and UMA18-FEDERJA-042 from UMA-FEDER & ALIANZA MIXTA ANDALUCÍA-ROCHE. Alicia González González is a recipient of a postdoctoral grant Margarita Salas (RMS-08) from European Union-NextGenerationEU, Spanish Ministry of Universities and Recovery Transformation and Resilience Plan, through a call from University of Cantabria. Aurora Laborda Illanes is a recipient of a predoctoral grant, PFIS-ISCIII (FI19–00112), co-funded by the Fondo Social Europeo (FSE). Lidia Sanchez Alcoholado is a recipient of a postdoctoral grant (RH-0026–2021) from the Consejería de Salud y Familia (co-funded by the Fondo Europeo de Andalucía 2014–2020, Andalucía, Spain). Daniel Castellano Castillo is a recipient of a postdoctoral grant Sara Borrell (CD21/00164) from Instituto de Salud Carlos III.es_ES
dc.format.extent7 p.es_ES
dc.language.isoenges_ES
dc.publisherEditions Scientifiques Elsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights© 2022 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license.*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceBiomedicine & Pharmacotherapy Volume 157, January 2023, 114041es_ES
dc.subject.otherAngiogenesis assayes_ES
dc.subject.otherAngiogenesis inhibitores_ES
dc.subject.otherBreast canceres_ES
dc.subject.otherCAMes_ES
dc.subject.otherChicken chorioallantoic membranees_ES
dc.subject.otherEndothelial cellses_ES
dc.subject.otherHUVECes_ES
dc.subject.otherMCF-7es_ES
dc.subject.otherMelatonines_ES
dc.subject.otherSpheroidses_ES
dc.subject.otherVEGFes_ES
dc.titleDevelopment of in vitro and in vivo tools to evaluate the antiangiogenic potential of melatonin to neutralize the angiogenic effects of VEGF and breast cancer cells: CAM assay and 3D endothelial cell spheroidses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.biopha.2022.114041es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.biopha.2022.114041es_ES
dc.type.versionpublishedVersiones_ES


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