Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34257
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dc.contributor.authorÜvez, Ayça-
dc.contributor.authorEsener, Osman Behzat Burak-
dc.contributor.authorErkısa, Merve-
dc.contributor.authorKarakuş, Dilek-
dc.contributor.authorArmutak, Elif İlkay-
dc.date.accessioned2023-10-09T10:07:57Z-
dc.date.available2023-10-09T10:07:57Z-
dc.date.issued2020-
dc.identifier.citationÜvez, A. vd. (2020). "Synergistic interactions between resveratrol and doxorubicin inhibit angiogenesis both in vitro and in vivo". Polish Journal of Veterinary Sciences, 23(4), 571-580.en_US
dc.identifier.issn1505-1773-
dc.identifier.issn2300-2557-
dc.identifier.urihttps://doi.org/10.24425/pjvs.2020.135803-
dc.identifier.urihttps://journals.pan.pl/dlibra/publication/135803/edition/118729/content-
dc.identifier.urihttp://hdl.handle.net/11452/34257-
dc.description.abstractResveratrol is a polyphenolic compound which is found in many nutrients including grapes, peanuts, raspberries, and apples. Anti-proliferative, anti-angiogenic and apoptotic effects of resveratrol have been shown on various cancer cells. Doxorubicin is considered as one of the most effective anticancer agents and reveals its antitumor activity by induction of apoptosis and inhibition of angiogenesis. Our study reports for the first time the potent ability of resveratrol in combination with doxorubicin to inhibit angiogenesis in vitro and in vivo. The cytotoxic effect of resveratrol (1.56-100 mu M), doxorubicin (0.01-0.92 mu M) and their combination were analyzed in the human umbilical vein endothelial cells (HUVECs) by ATP assay. In vitro angiogenesis was evaluated using tube formation assay in HUVECs. In vivo anti-angiogenic activity was assessed in a chick chorioallantoic membrane (CAM) model using fertilized chicken eggs. All test groups were compared to thalidomide as a positive control, three concentrations of resveratrol (10-5-2.5 mu g/pellet) and a 2 mu g/pellet concentration of doxorubicin was examined. All data were evaluated statistically. Resveratrol and doxorubicin alone displayed inhibitory effects on angiogenesis and cell viability at higher doses. However, the combination of resveratrol and doxorubicin exhibited a significant dose-dependent inhibition of CAM angiogenesis in vivo as well as proliferation and tube formation in HUVECs compared to the positive control (+/-)-thalidomide. Our results suggest that resveratrol in combination with doxorubicin is a novel strategy in the prevention and treatment of angiogenesis.en_US
dc.language.isoenen_US
dc.publisherPolska Akademia Nauken_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectVeterinary sciencesen_US
dc.subjectResveratrolen_US
dc.subjectAnti-angiogenic activityen_US
dc.subjectTube formationen_US
dc.subjectHuvecen_US
dc.subjectDoxorubicinen_US
dc.subjectChick chorioallantoic membraneen_US
dc.subjectCanceren_US
dc.subjectCombinationen_US
dc.subjectApoptosisen_US
dc.subjectGrowthen_US
dc.subjectChemotraphyen_US
dc.subjectCellsen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAntibioticsen_US
dc.subject.meshAntineoplasticen_US
dc.subject.meshChorioallantoic membraneen_US
dc.subject.meshDrug synergismen_US
dc.subject.meshHuman umbilical vein endothelial cellsen_US
dc.subject.meshNeovascularizationen_US
dc.subject.meshPhysiologicen_US
dc.subject.meshResveratrolen_US
dc.titleSynergistic interactions between resveratrol and doxorubicin inhibit angiogenesis both in vitro and in vivoen_US
dc.typeArticleen_US
dc.identifier.wos000604955100012tr_TR
dc.identifier.scopus2-s2.0-85100328107tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.contributor.orcid0000-0001-5238-2432tr_TR
dc.identifier.startpage571tr_TR
dc.identifier.endpage580tr_TR
dc.identifier.volume23tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalPolish Journal of Veterinary Sciencesen_US
dc.contributor.buuauthorAydınlık, Şeyma-
dc.contributor.researcheridABI-2909-2020tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed33480492tr_TR
dc.subject.wosVeterinary sciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid57190280044tr_TR
dc.subject.scopusResveratrol; Resveratrol-4'-O-Glucuronide; Stilbene Derivativeen_US
dc.subject.emtreeAdenosine triphosphaten_US
dc.subject.emtreeDoxorubicinen_US
dc.subject.emtreeResveratrolen_US
dc.subject.emtreeThalidomideen_US
dc.subject.emtreeAntineoplastic antibioticen_US
dc.subject.emtreeAntioxidanten_US
dc.subject.emtreeDoxorubicinen_US
dc.subject.emtreeResveratrolen_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAntiangiogenic activityen_US
dc.subject.emtreeAntiproliferative activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCell viabilityen_US
dc.subject.emtreeChick embryoen_US
dc.subject.emtreeChorioallantoisen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug cytotoxicityen_US
dc.subject.emtreeDrug potentiationen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreeIn vivo studyen_US
dc.subject.emtreeMouseen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeUmbilical vein endothelial cellen_US
dc.subject.emtreeAngiogenesisen_US
dc.subject.emtreeAnimalen_US
dc.subject.emtreeAngiogenesisen_US
dc.subject.emtreeCell proliferationen_US
dc.subject.emtreeCell survivalen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeDrug potentiationen_US
dc.subject.emtreeVascularizationen_US
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