Publication:
OT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesis

dc.contributor.authorRebbaa, Abdelhadi
dc.contributor.authorPatil, Ghanshyam
dc.contributor.authorSudha, Thangirala
dc.contributor.authorMousa, Shaker A.
dc.contributor.buuauthorYalçın, Murat
dc.contributor.departmentVeterinerlik Fakültesi
dc.contributor.departmentVeteriner Hekimliği Temel Bilimler Bölümü
dc.contributor.orcid0000-0002-5600-8162
dc.contributor.researcheridAAG-6956-2021
dc.contributor.scopusid57192959734
dc.date.accessioned2023-05-26T07:58:17Z
dc.date.available2023-05-26T07:58:17Z
dc.date.issued2013-05
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.
dc.description.sponsorshipOthera Pharmaceuticals
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.
dc.identifier.endpage62
dc.identifier.issn0304-3835
dc.identifier.issn1872-7980
dc.identifier.issue1
dc.identifier.pubmed23348692
dc.identifier.scopus2-s2.0-84875255335
dc.identifier.startpage55
dc.identifier.urihttps://doi.org/10.1016/j.canlet.2013.01.016
dc.identifier.urihttp://hdl.handle.net/11452/32804
dc.identifier.volume332
dc.identifier.wos000316775500008
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.collaborationYurtdışı
dc.relation.journalCancer Letters
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectOncology
dc.subjectAngiogenesis
dc.subjectChemo-resistance
dc.subjectNanoparticles
dc.subjectOT-404
dc.subjectHormone-releasing-hormone
dc.subjectEndothelial growth-factor
dc.subjectThyroid-hormone
dc.subjectProngiogenic action
dc.subjectKinase inhibitor
dc.subjectTyrosine kinase
dc.subjectDown-regülation
dc.subjectCancer-therapy
dc.subjectPhase-II
dc.subjectIn-vivo
dc.subjectMus musculus
dc.subject.emtreeAntineoplastic agent
dc.subject.emtreeDoxorubicin
dc.subject.emtreeEtoposide
dc.subject.emtreeFibroblast growth factor 2
dc.subject.emtreeNanoparticle
dc.subject.emtreeOt 404
dc.subject.emtreeUnclassified drug
dc.subject.emtreeAnimal cell
dc.subject.emtreeAnimal experiment
dc.subject.emtreeAntineoplastic activity
dc.subject.emtreeArticle
dc.subject.emtreeBreast cancer
dc.subject.emtreeCancer cell
dc.subject.emtreeCancer growth
dc.subject.emtreeCarcinogenesis
dc.subject.emtreeControlled study
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug mechanism
dc.subject.emtreeDrug targeting
dc.subject.emtreeHuman
dc.subject.emtreeHuman cell
dc.subject.emtreeIn vivo study
dc.subject.emtreeMale
dc.subject.emtreeMouse
dc.subject.emtreeNonhuman
dc.subject.emtreePriority journal
dc.subject.emtreeTumor growth
dc.subject.emtreeTumor volume
dc.subject.emtreeTumor xenograft
dc.subject.meshAngiogenesis inhibitors
dc.subject.meshAnimals
dc.subject.meshAntineoplastic combined chemotherapy protocols
dc.subject.meshBreast neoplasms
dc.subject.meshCell proliferation
dc.subject.meshChemistry, pharmaceutical
dc.subject.meshDose-response relationship, drug
dc.subject.meshDoxorubicin
dc.subject.meshDrug resistance, neoplasm
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMCF-7 cells
dc.subject.meshMice
dc.subject.meshMice, inbred C57BL
dc.subject.meshMice, nude
dc.subject.meshNanocapsules
dc.subject.meshNeovascularization, physiologic
dc.subject.meshTime factors
dc.subject.meshTumor burden
dc.subject.meshU937 cells
dc.subject.meshXenograft model antitumor assays
dc.subject.scopusHsp90 Inhibitor; Ganetespib; Tanespimycin
dc.subject.wosOncology
dc.titleOT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesis
dc.typeArticle
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentVeterinerlik Fakültesi/Veteriner Hekimliği Temel Bilimler Bölümü
local.indexed.atScopus
local.indexed.atWOS

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