Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29660
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dc.contributor.authorKaçar, Ömer-
dc.contributor.authorAdıgüzel, Zelal-
dc.contributor.authorAçılan, Ceyda-
dc.date.accessioned2022-12-05T07:13:09Z-
dc.date.available2022-12-05T07:13:09Z-
dc.date.issued2013-07-
dc.identifier.citationCevatemre, B. vd. (2013). ''Combination of fenretinide and indole-3-carbinol results in synergistic cytotoxic activity inducing apoptosis against human breast cancer cells in vitro". Anti-Cancer Drugs, 24(6), 577-586.en_US
dc.identifier.issn0959-4973-
dc.identifier.issn1473-5741-
dc.identifier.urihttps://doi.org/10.1097/CAD.0b013e328360a921-
dc.identifier.urihttps://journals.lww.com/anti-cancerdrugs/Fulltext/2013/07000/Combination_of_fenretinide_and_indole_3_carbinol.4.aspx-
dc.identifier.urihttp://hdl.handle.net/11452/29660-
dc.description.abstractThe outcome in patients with breast cancer is not satisfactory to date, although new chemotherapy regimens have been introduced in clinics. Therefore, novel approaches are required for better management of patients with breast cancer. In this study, we tested the cytotoxic activity of a new combination of fenretinide, a synthetic retinoid, with indole-3-carbinol, a natural product present in vegetables such as broccoli and cabbage, against MCF-7 (estrogen receptor-positive) and MDA-MB-231 (estrogen receptor-negative) cell lines. It has been found that the combination resulted in more powerful cytotoxic activity, by induction of apoptosis, compared with that when they were used singly. In conclusion, this novel combination warrants in-vivo experiments to elucidate its possible use in the treatment of breast cancer.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinstr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOncologyen_US
dc.subjectPharmacology & pharmacyen_US
dc.subject3,3 '-diindolylmethaneen_US
dc.subjectBreast canceren_US
dc.subjectChemotherapyen_US
dc.subjectCytotoxicityen_US
dc.subjectFenretinide (4-HPR)en_US
dc.subjectIndole-3-carbinolen_US
dc.subjectGene-expressionen_US
dc.subjectDown-regulationen_US
dc.subjectOvarian-canceren_US
dc.subjectCycle arresten_US
dc.subjectGrowthen_US
dc.subject3,3'-diindolylmethaneen_US
dc.subjectDeathen_US
dc.subjectInductionen_US
dc.subject3,3-diindolylmethaneen_US
dc.subjectInhibitionen_US
dc.subject.meshAntineoplastic agentsen_US
dc.subject.meshApoptosisen_US
dc.subject.meshCell cycleen_US
dc.subject.meshDNA, complementaryen_US
dc.subject.meshDrug synergismen_US
dc.subject.meshFenretinideen_US
dc.subject.meshGene expression regulation, neoplasticen_US
dc.subject.meshHumansen_US
dc.subject.meshIndolesen_US
dc.subject.meshMCF-7 cellsen_US
dc.subject.meshRNAen_US
dc.subject.meshRNA, small interferingen_US
dc.subject.meshTransfectionen_US
dc.titleCombination of fenretinide and indole-3-carbinol results in synergistic cytotoxic activity inducing apoptosis against human breast cancer cells in vitroen_US
dc.typeArticleen_US
dc.identifier.wos000323214000004tr_TR
dc.identifier.scopus2-s2.0-84878902921tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.relation.bapUAP(F)-2011/44tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.orcid0000-0003-0463-6818tr_TR
dc.identifier.startpage577tr_TR
dc.identifier.endpage586tr_TR
dc.identifier.volume24tr_TR
dc.identifier.issue6tr_TR
dc.relation.journalAnti-Cancer Drugstr_TR
dc.contributor.buuauthorCevatemre, Buse-
dc.contributor.buuauthorArı, Ferda-
dc.contributor.buuauthorSarımahmut, Mehmet-
dc.contributor.buuauthorOral, Arzu Yılmaztepe-
dc.contributor.buuauthorDere, Egemen-
dc.contributor.buuauthorUlukaya, Engin-
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.contributor.researcheridAHD-2050-2022tr_TR
dc.contributor.researcheridAAH-5068-2021tr_TR
dc.contributor.researcheridK-5792-2018tr_TR
dc.contributor.researcheridA-5841-2017tr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed23542749tr_TR
dc.subject.wosOncologyen_US
dc.subject.wosPharmacology & pharmacyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid55693788600tr_TR
dc.contributor.scopusid2437608530tr_TR
dc.contributor.scopusid44661687400tr_TR
dc.contributor.scopusid23091316500tr_TR
dc.contributor.scopusid6603627015tr_TR
dc.contributor.scopusid6602927353tr_TR
dc.subject.scopus3 Indolemethanol; Indoles; 3-(2-Bromoethyl)Indoleen_US
dc.subject.emtree3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromideen_US
dc.subject.emtree3 indolemethanolen_US
dc.subject.emtreeAdenosine triphosphateen_US
dc.subject.emtreeFenretinideen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBreast canceren_US
dc.subject.emtreeBroccolien_US
dc.subject.emtreeCabbageen_US
dc.subject.emtreeCell deathen_US
dc.subject.emtreeCell viabilityen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug cytotoxicityen_US
dc.subject.emtreeEstrogen receptor positive breast canceren_US
dc.subject.emtreeFluorescence imagingen_US
dc.subject.emtreeGene expressionen_US
dc.subject.emtreeGenetic transfectionen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeWestern blottingen_US
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