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dc.contributor.author정낙신-
dc.date.accessioned2016-08-28T10:08:20Z-
dc.date.available2016-08-28T10:08:20Z-
dc.date.issued2013-
dc.identifier.issn0006-291X-
dc.identifier.otherOAK-10327-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223928-
dc.description.abstractAlthough A3AR agonists exhibit a variety of biological activities including anticancer effects, their possible anti-angiogenic effects have not yet been investigated. In the present study, we assayed the anti-angiogenic activity of thio-Cl-IB-MECA, a novel A3AR agonist, in cultured HUVECs and mES/EB-derived endothelial cells. Thio-Cl-IB-MECA inhibited migration and tube formation by endothelial cells and dramatically decreased ex vivo microvessel sprouting in cultured mouse aortic rings. The anti-angiogenic activity of thio-Cl-IB-MECA was associated with suppression of the expression of the endothelial biomarker PECAM via regulation of PI3K/AKT/mTOR and ERK signaling in mES/EB-derived endothelial cells. © 2013 Elsevier Inc.-
dc.languageEnglish-
dc.titleThio-Cl-IB-MECA, a novel A3 adenosine receptor agonist, suppresses angiogenesis by regulating PI3K/AKT/mTOR and ERK signaling in endothelial cells-
dc.typeArticle-
dc.relation.issue1-
dc.relation.volume437-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage79-
dc.relation.lastpage86-
dc.relation.journaltitleBiochemical and Biophysical Research Communications-
dc.identifier.doi10.1016/j.bbrc.2013.06.040-
dc.identifier.wosidWOS:000322353000014-
dc.identifier.scopusid2-s2.0-84880506278-
dc.author.googleKim G.D.-
dc.author.googleOh J.-
dc.author.googleJeong L.S.-
dc.author.googleLee S.K.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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