Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33037
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dc.contributor.authorYurdacan, Beste-
dc.contributor.authorEskiler, Gamze Güney-
dc.date.accessioned2023-06-14T12:41:23Z-
dc.date.available2023-06-14T12:41:23Z-
dc.date.issued2019-07-
dc.identifier.citationYurdacan, B. vd. (2019). ''Investigation of new treatment option for hepatocellular carcinoma: a combination of sorafenib with usnic acid''. Journal of Pharmacy and Pharmacology, 71(7), 1119-1132.en_US
dc.identifier.issn0022-3573-
dc.identifier.issn2042-7158-
dc.identifier.urihttps://doi.org/10.1111/jphp.13097-
dc.identifier.urihttps://academic.oup.com/jpp/article/71/7/1119/6122173-
dc.identifier.urihttp://hdl.handle.net/11452/33037-
dc.description.abstractObjectives Sorafenib (SOR) is an orally administered molecular targeted agent in the systemic chemotherapy of hepatocellular carcinoma (HCC). However, the partial response of SOR is limited due to its adverse side effect and high heterogeneity and resistant phenotype of HCC. In the current study, we investigated synergistic effects of SOR and usnic acid (UA) on HCC cell lines including HepG2 and SNU-449, and a normal cell line, HUVEC. Methods The antiproliferative and apoptotic effects of combination therapy and SOR alone were analysed by WST-1 and Annexin V analysis, respectively. Furthermore, cell cycle, gene expression analysis of SOR-targeted kinases and acridine orange-ethidium bromide staining were also performed in combined treatments. Key findings Our results demonstrated that SOR and UA combination indicated a strong synergism in HCC cell lines and reduced SOR toxicity in HUVEC cells. Additionally, the combination treatment SOR and UA significantly induced much more apoptotic cell death and G0/G1 arrest through downregulation of SOR-targeted kinases. Conclusions Consequently, SOR and UA combination could be a new therapeutic strategy for HCC treatment.tr_TR
dc.language.isoenen_US
dc.publisherOxford Universityen_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.subjectCombination treatmenten_US
dc.subjectHepatocellular carcinomaen_US
dc.subjectSorafeniben_US
dc.subjectUsnic aciden_US
dc.subjectAntitumor-activityen_US
dc.subjectCancer-cellsen_US
dc.subjectInhibitionen_US
dc.subjectPathwayen_US
dc.subjectGeneen_US
dc.subjectP16en_US
dc.subjectPharmacology & pharmacyen_US
dc.subject.meshAnnexin A5en_US
dc.subject.meshAntineoplastic Agentsen_US
dc.subject.meshApoptosisen_US
dc.subject.meshBenzofuransen_US
dc.subject.meshCarcinoma, Hepatocellularen_US
dc.subject.meshCell Line, Tumoren_US
dc.subject.meshCell Proliferationen_US
dc.subject.meshDrug Synergismen_US
dc.subject.meshDrug Therapy, Combinationen_US
dc.subject.meshHep G2 Cellsen_US
dc.subject.meshHumansen_US
dc.subject.meshLiver Neoplasmsen_US
dc.subject.meshProtein-Tyrosine Kinasesen_US
dc.subject.meshSorafeniben_US
dc.titleInvestigation of new treatment option for hepatocellular carcinoma: A combination of sorafenib with usnic aciden_US
dc.typeArticleen_US
dc.identifier.wos000470977400010tr_TR
dc.identifier.scopus2-s2.0-85065044797tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri/Tıbbi Biyoloji Bölümü.tr_TR
dc.contributor.orcid0000-0002-1619-6680tr_TR
dc.contributor.orcid0000-0002-3820-424Xtr_TR
dc.contributor.orcid0000-0002-3316-316Xtr_TR
dc.contributor.orcid0000-0002-3316-316Xtr_TR
dc.contributor.orcid0000-0001-7904-883Xtr_TR
dc.identifier.startpage1119tr_TR
dc.identifier.endpage1132tr_TR
dc.identifier.volume71tr_TR
dc.identifier.issue7tr_TR
dc.relation.journalJournal of Pharmacy and Pharmacologyen_US
dc.contributor.buuauthorEgeli, Ünal-
dc.contributor.buuauthorEryılmaz, Işıl Ezgi-
dc.contributor.buuauthorÇeçener, Gülşah-
dc.contributor.buuauthorTunca, Berrin-
dc.contributor.researcheridABI-6078-2020tr_TR
dc.contributor.researcheridAAP-9988-2020tr_TR
dc.contributor.researcheridGWV-3548-2022tr_TR
dc.contributor.researcheridAAH-1656-2021tr_TR
dc.contributor.researcheridAAH-1420-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed31025377tr_TR
dc.subject.wosPharmacology & pharmacyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid55665145000tr_TR
dc.contributor.scopusid57189380840tr_TR
dc.contributor.scopusid6508156530tr_TR
dc.contributor.scopusid6602965754tr_TR
dc.subject.scopusUsnic Acid; Extract; Lichen (Disease)en_US
dc.subject.emtreeAcridine orangeen_US
dc.subject.emtreeEthidium bromideen_US
dc.subject.emtreeLipocortin 5en_US
dc.subject.emtreePhosphotransferaseen_US
dc.subject.emtreeSorafeniben_US
dc.subject.emtreeUsnic aciden_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeBenzofuran derivativeen_US
dc.subject.emtreeProtein tyrosine kinaseen_US
dc.subject.emtreeAntiproliferative activityen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeAutophagyen_US
dc.subject.emtreeCell cycle arresten_US
dc.subject.emtreeCell organelleen_US
dc.subject.emtreeCell structureen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDown regulationen_US
dc.subject.emtreeDrug cytotoxicityen_US
dc.subject.emtreeDrug potentiationen_US
dc.subject.emtreeGene expressionen_US
dc.subject.emtreeHep-G2 cell lineen_US
dc.subject.emtreeHepatocellular carcinoma cell lineen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeHUVEC cell lineen_US
dc.subject.emtreeLiver cell carcinomaen_US
dc.subject.emtreePercentage of cells in G0/G1 phaseen_US
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreeCell proliferationen_US
dc.subject.emtreeCombination drug therapyen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeLiver cell carcinomaen_US
dc.subject.emtreeLiver tumoren_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreeTumor cell lineen_US
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