Mostrar el registro sencillo del ítem

Artículo

dc.creatorFernández Cruz, Edwines
dc.creatorCerezo López, Ana Belénes
dc.creatorCantos Villar, Emmaes
dc.creatorRichard, Tristanes
dc.creatorTroncoso González, Ana Maríaes
dc.creatorGarcía Parrilla, María del Carmenes
dc.date.accessioned2023-12-18T15:53:48Z
dc.date.available2023-12-18T15:53:48Z
dc.date.issued2019-04
dc.identifier.citationFernández Cruz, E., Cerezo López, A.B., Cantos Villar, E., Richard, T., Troncoso González, A.M. y García Parrilla, M.d.C. (2019). Inhibition of VEGFR-2 Phosphorylation and Effects on Downstream Signaling Pathways in Cultivated Human Endothelial Cells by Stilbenes from Vitis Spp. Journal of Agricultural and Food Chemistry, 67 (14), 3909-3918. https://doi.org/10.1021/acs.jafc.9b00282.
dc.identifier.issn0021-8561es
dc.identifier.issn1520-5118es
dc.identifier.urihttps://hdl.handle.net/11441/152650
dc.description.abstractStilbenes are phenolic compounds present in different higher plant families that have shown different biological activities, such as antioxidant properties and antitumoral and anti-atherosclerotic effects, among others. Angiogenesis is a key process involved in both cancer and cardiovascular diseases, the vascular endothelial growth factor (VEGF) and its receptor VEGFR-2 being the main triggers. Certain polyphenol compounds, such as flavonoids, have shown a potent capacity to inhibit VEGF and, consequently, angiogenesis. The present work, therefore, aims to evaluate the potential effect of stilbenes on inhibiting VEGF and their subsequent effect on the downstream signaling pathway (PLCγ1, Akt, and eNOS). VEGFR-2 activation was studied through an ELISA assay in the HUVEC line, while the phosphorylation of intracellular downstream proteins PLCγ1, Akt, and eNOS was tested by Western blot. Student's t test was used to determine significant differences between samples. On the one hand, astringin, pallidol, and -viniferin showed the lowest IC 50 values (2.90 ± 0.27, 4.42 ± 0.67, and 6.10 ± 1.29 μM, respectively) against VEGFR-2 activation. Additionally, VEGF-induced PLCγ1 phosphorylation was significantly inhibited by ϵ-viniferin, astringin, and -viniferin. However, ϵ-viniferin and pallidol simultaneously enhanced eNOS activation, proving to be via Akt activation in the case of ϵ-viniferin. For the first time, these data suggest that stilbenes such as astringin, pallidol, -viniferin, and ϵ-viniferin have a potential anti-angiogenic effect and they could be further considered as anti-VEGF ingredients in food and beverages. In addition, ϵ ϵ-viniferin and pallidol significantly allowed eNOS activation and could likely prevent the side effects caused by anti-VEGF hypertension drugs.es
dc.description.sponsorshipEuropean Union PP.AVA.AVA201601.03es
dc.description.sponsorshipAgence nationale de la recherche ANR-14-LAB5-0005-01, ANR-11-INBS-0010es
dc.formatapplication/pdfes
dc.format.extent35 p.es
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.relation.ispartofJournal of Agricultural and Food Chemistry, 67 (14), 3909-3918.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAnti-angiogenices
dc.subjectAstringines
dc.subjectHUVECes
dc.subjectStilbeneses
dc.subjectVEGFes
dc.titleInhibition of VEGFR-2 Phosphorylation and Effects on Downstream Signaling Pathways in Cultivated Human Endothelial Cells by Stilbenes from Vitis Sppes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Nutrición y Bromatología, Toxicología y Medicina Legales
dc.relation.projectIDPP.AVA.AVA201601.03es
dc.relation.projectIDANR-14-LAB5-0005-01es
dc.relation.projectIDANR-11-INBS-0010es
dc.relation.publisherversionhttps://doi.org/10.1021/acs.jafc.9b00282es
dc.identifier.doi10.1021/acs.jafc.9b00282es
dc.journaltitleJournal of Agricultural and Food Chemistryes
dc.publication.volumen67es
dc.publication.issue14es
dc.publication.initialPage3909es
dc.publication.endPage3918es
dc.contributor.funderEuropean Union (UE)es
dc.contributor.funderAgence Nationale de la Recherche. Francees

FicherosTamañoFormatoVerDescripción
Inhibition of VEGFR‑2.pdf1.077MbIcon   [PDF] Ver/Abrir   Versión aceptada

Este registro aparece en las siguientes colecciones

Mostrar el registro sencillo del ítem

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