Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/32804
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dc.contributor.authorRebbaa, Abdelhadi-
dc.contributor.authorPatil, Ghanshyam-
dc.contributor.authorSudha, Thangirala-
dc.contributor.authorMousa, Shaker A.-
dc.date.accessioned2023-05-26T07:58:17Z-
dc.date.available2023-05-26T07:58:17Z-
dc.date.issued2013-05-
dc.identifier.citationRebbaa, A. vd. (2013). “OT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesis”. Cancer Letters, 332(1), 55-62.en_US
dc.identifier.issn0304-3835-
dc.identifier.issn1872-7980-
dc.identifier.urihttps://doi.org/10.1016/j.canlet.2013.01.016-
dc.identifier.urihttp://hdl.handle.net/11452/32804-
dc.description.abstractThere is a need for a comprehensive anti-cancer strategy that simultaneously targets abnormal proliferation, angiogenesis rates, and development of chemotherapy resistance. We have identified a small molecule, OT-404, that effectively inhibited proliferation and angiogenesis of either chemo-sensitive or resistant human cancer cells and enhanced cancer cell sensitivity to different chemotherapy. In vivo studies of human tumor xenografts in nude mice showed that OT-404, used alone or encapsulated into nanoparticles, inhibited the growth of doxorubicin-resistant breast cancer MCF-7 by more than 80%, and by 95% when combined with doxorubicin. These findings provide evidence for the potential of OT-404 in cancer management.en_US
dc.description.sponsorshipOthera Pharmaceuticalsen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOncologyen_US
dc.subjectAngiogenesisen_US
dc.subjectChemo-resistanceen_US
dc.subjectNanoparticlesen_US
dc.subjectOT-404en_US
dc.subjectHormone-releasing-hormoneen_US
dc.subjectEndothelial growth-factoren_US
dc.subjectThyroid-hormoneen_US
dc.subjectProngiogenic actionen_US
dc.subjectKinase inhibitoren_US
dc.subjectTyrosine kinaseen_US
dc.subjectDown-regülationen_US
dc.subjectCancer-therapyen_US
dc.subjectPhase-IIen_US
dc.subjectIn-vivoen_US
dc.subjectMus musculusen_US
dc.subject.meshAngiogenesis inhibitorsen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAntineoplastic combined chemotherapy protocolsen_US
dc.subject.meshBreast neoplasmsen_US
dc.subject.meshCell proliferationen_US
dc.subject.meshChemistry, pharmaceuticalen_US
dc.subject.meshDose-response relationship, drugen_US
dc.subject.meshDoxorubicinen_US
dc.subject.meshDrug resistance, neoplasmen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMCF-7 cellsen_US
dc.subject.meshMiceen_US
dc.subject.meshMice, inbred C57BLen_US
dc.subject.meshMice, nudeen_US
dc.subject.meshNanocapsulesen_US
dc.subject.meshNeovascularization, physiologicen_US
dc.subject.meshTime factorsen_US
dc.subject.meshTumor burdenen_US
dc.subject.meshU937 cellsen_US
dc.subject.meshXenograft model antitumor assaysen_US
dc.titleOT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesisen_US
dc.typeArticleen_US
dc.identifier.wos000316775500008tr_TR
dc.identifier.scopus2-s2.0-84875255335tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Veterinerlik Fakültesi/Veteriner Hekimliği Temel Bilimler Bölümü.tr_TR
dc.contributor.orcid0000-0002-5600-8162tr_TR
dc.identifier.startpage55tr_TR
dc.identifier.endpage62tr_TR
dc.identifier.volume332tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalCancer Lettersen_US
dc.contributor.buuauthorYalçın, Murat-
dc.contributor.researcheridAAG-6956-2021tr_TR
dc.relation.collaborationYurtdışıtr_TR
dc.identifier.pubmed23348692tr_TR
dc.subject.wosOncologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ1en_US
dc.contributor.scopusid57192959734tr_TR
dc.subject.scopusHsp90 Inhibitor; Ganetespib; Tanespimycinen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeDoxorubicinen_US
dc.subject.emtreeEtoposideen_US
dc.subject.emtreeFibroblast growth factor 2en_US
dc.subject.emtreeNanoparticleen_US
dc.subject.emtreeOt 404en_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAntineoplastic activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBreast canceren_US
dc.subject.emtreeCancer cellen_US
dc.subject.emtreeCancer growthen_US
dc.subject.emtreeCarcinogenesisen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug mechanismen_US
dc.subject.emtreeDrug targetingen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIn vivo studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMouseen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeTumor growthen_US
dc.subject.emtreeTumor volumeen_US
dc.subject.emtreeTumor xenograften_US
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