Publication: OT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesis
dc.contributor.author | Rebbaa, Abdelhadi | |
dc.contributor.author | Patil, Ghanshyam | |
dc.contributor.author | Sudha, Thangirala | |
dc.contributor.author | Mousa, Shaker A. | |
dc.contributor.buuauthor | Yalçın, Murat | |
dc.contributor.department | Veterinerlik Fakültesi | |
dc.contributor.department | Veteriner Hekimliği Temel Bilimler Bölümü | |
dc.contributor.orcid | 0000-0002-5600-8162 | |
dc.contributor.researcherid | AAG-6956-2021 | |
dc.contributor.scopusid | 57192959734 | |
dc.date.accessioned | 2023-05-26T07:58:17Z | |
dc.date.available | 2023-05-26T07:58:17Z | |
dc.date.issued | 2013-05 | |
dc.description.abstract | There 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.sponsorship | Othera Pharmaceuticals | |
dc.identifier.citation | Rebbaa, 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.endpage | 62 | |
dc.identifier.issn | 0304-3835 | |
dc.identifier.issn | 1872-7980 | |
dc.identifier.issue | 1 | |
dc.identifier.pubmed | 23348692 | |
dc.identifier.scopus | 2-s2.0-84875255335 | |
dc.identifier.startpage | 55 | |
dc.identifier.uri | https://doi.org/10.1016/j.canlet.2013.01.016 | |
dc.identifier.uri | http://hdl.handle.net/11452/32804 | |
dc.identifier.volume | 332 | |
dc.identifier.wos | 000316775500008 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.relation.collaboration | Yurtdışı | |
dc.relation.journal | Cancer Letters | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Oncology | |
dc.subject | Angiogenesis | |
dc.subject | Chemo-resistance | |
dc.subject | Nanoparticles | |
dc.subject | OT-404 | |
dc.subject | Hormone-releasing-hormone | |
dc.subject | Endothelial growth-factor | |
dc.subject | Thyroid-hormone | |
dc.subject | Prongiogenic action | |
dc.subject | Kinase inhibitor | |
dc.subject | Tyrosine kinase | |
dc.subject | Down-regülation | |
dc.subject | Cancer-therapy | |
dc.subject | Phase-II | |
dc.subject | In-vivo | |
dc.subject | Mus musculus | |
dc.subject.emtree | Antineoplastic agent | |
dc.subject.emtree | Doxorubicin | |
dc.subject.emtree | Etoposide | |
dc.subject.emtree | Fibroblast growth factor 2 | |
dc.subject.emtree | Nanoparticle | |
dc.subject.emtree | Ot 404 | |
dc.subject.emtree | Unclassified drug | |
dc.subject.emtree | Animal cell | |
dc.subject.emtree | Animal experiment | |
dc.subject.emtree | Antineoplastic activity | |
dc.subject.emtree | Article | |
dc.subject.emtree | Breast cancer | |
dc.subject.emtree | Cancer cell | |
dc.subject.emtree | Cancer growth | |
dc.subject.emtree | Carcinogenesis | |
dc.subject.emtree | Controlled study | |
dc.subject.emtree | Drug efficacy | |
dc.subject.emtree | Drug mechanism | |
dc.subject.emtree | Drug targeting | |
dc.subject.emtree | Human | |
dc.subject.emtree | Human cell | |
dc.subject.emtree | In vivo study | |
dc.subject.emtree | Male | |
dc.subject.emtree | Mouse | |
dc.subject.emtree | Nonhuman | |
dc.subject.emtree | Priority journal | |
dc.subject.emtree | Tumor growth | |
dc.subject.emtree | Tumor volume | |
dc.subject.emtree | Tumor xenograft | |
dc.subject.mesh | Angiogenesis inhibitors | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Antineoplastic combined chemotherapy protocols | |
dc.subject.mesh | Breast neoplasms | |
dc.subject.mesh | Cell proliferation | |
dc.subject.mesh | Chemistry, pharmaceutical | |
dc.subject.mesh | Dose-response relationship, drug | |
dc.subject.mesh | Doxorubicin | |
dc.subject.mesh | Drug resistance, neoplasm | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | MCF-7 cells | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mice, inbred C57BL | |
dc.subject.mesh | Mice, nude | |
dc.subject.mesh | Nanocapsules | |
dc.subject.mesh | Neovascularization, physiologic | |
dc.subject.mesh | Time factors | |
dc.subject.mesh | Tumor burden | |
dc.subject.mesh | U937 cells | |
dc.subject.mesh | Xenograft model antitumor assays | |
dc.subject.scopus | Hsp90 Inhibitor; Ganetespib; Tanespimycin | |
dc.subject.wos | Oncology | |
dc.title | OT-404, multi-targeted anti-cancer agent affecting tumor proliferation, chemo-resistance, and angiogenesis | |
dc.type | Article | |
dc.wos.quartile | Q1 | |
dspace.entity.type | Publication | |
local.contributor.department | Veterinerlik Fakültesi/Veteriner Hekimliği Temel Bilimler Bölümü | |
local.indexed.at | Scopus | |
local.indexed.at | WOS |
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