Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29462
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dc.date.accessioned2022-11-16T13:30:24Z-
dc.date.available2022-11-16T13:30:24Z-
dc.date.issued2013-06-
dc.identifier.citationArı, F. vd. (2013). "Palladium(II) saccharinate complexes with bis(2-pyridylmethyl) amine induce cell death by apoptosis in human breast cancer cells in vitro", Bioorganic and Medicinal Chemistry, 21(11), 3016-3021.en_US
dc.identifier.issn0968-0896-
dc.identifier.issn1464-3391-
dc.identifier.urihttps://doi.org/10.1016/j.bmc.2013.03.073-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0968089613002952-
dc.identifier.urihttp://hdl.handle.net/11452/29462-
dc.description.abstractThe outcomes of breast cancer patients are still poor although new compounds have recently been introduced into the clinic. Therefore, novel chemical approaches are required. In the present study, palladium( II) and corresponding platinum(II) complexes containing bis(2-pyridylmethyl) amine (bpma) and saccharine were synthesized and tested against human breast cancer cell lines, MCF-7 and MDA-MB-231, in vitro. Cytotoxicity was first screened by the MTT assay and the results were further confirmed by the ATP assay. The palladium complexes 1 and 3 yielded stronger cytotoxicity than the corresponding platinum complexes 2 and 4 at the same doses. The palladium complex 3 was found to be the most cytotoxic one. Therefore, a more comprehensive study was carried out with this complex only. The mode of cell death was determined morphologically under fluorescent microscope and biochemically with detection of active caspase-3 and PARP cleavage by Western blot. Changes in apoptosis-related gene expressions were measured with qPCR. It was demonstrated that complex 3 caused cell death by apoptosis determined by fluorescence imaging and Western blot. As a sign of apoptosis, PARP was cleaved in both of the cell lines. In addition, caspase-3 was cleaved in MDA-MB-231 cells while this cleavage was not observed in MCF-7. The results show that the complex 3 is a promising anti-cancer compound against breast cancer with an IC50 value of 3.9 mu M for MCF-7 and 4.2 mu M for MDA-MB-231 cells, which warrants further animal experiments.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiochemistry & molecular biologyen_US
dc.subjectPharmacology & pharmacyen_US
dc.subjectChemistryen_US
dc.subject.meshAntineoplastic agentsen_US
dc.subject.meshApoptosisen_US
dc.subject.meshCaspase 3en_US
dc.subject.meshCell line, tumoren_US
dc.subject.meshCell proliferationen_US
dc.subject.meshCoordination complexesen_US
dc.subject.meshCytotoxinsen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene expressionen_US
dc.subject.meshHumansen_US
dc.subject.meshInhibitory concentration 50en_US
dc.subject.meshOrganoplatinum compoundsen_US
dc.subject.meshPalladiumen_US
dc.subject.meshPoly(ADP-ribose) polymerasesen_US
dc.titlePalladium(II) saccharinate complexes with bis(2-pyridylmethyl) amine induce cell death by apoptosis in human breast cancer cells in vitroen_US
dc.typeArticleen_US
dc.identifier.wos000319002600022tr_TR
dc.identifier.scopus2-s2.0-84877826586tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.relation.bapUAP(T)-2010-6tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.orcid0000-0002-2849-3332tr_TR
dc.contributor.orcid0000-0003-2647-5875tr_TR
dc.identifier.startpage3016tr_TR
dc.identifier.endpage3021tr_TR
dc.identifier.volume21tr_TR
dc.identifier.issue11tr_TR
dc.relation.journalBioorganic and Medicinal Chemistryen_US
dc.contributor.buuauthorArı, Ferda-
dc.contributor.buuauthorUlukaya, Engin-
dc.contributor.buuauthorSarımahmut, Mehmet-
dc.contributor.buuauthorYılmaz, Veysel Turan-
dc.contributor.researcheridAAG-8288-2021tr_TR
dc.contributor.researcheridL-7238-2018tr_TR
dc.contributor.researcheridK-5792-2018tr_TR
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.identifier.pubmed23601820tr_TR
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosChemistry, medicinalen_US
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid24376085300tr_TR
dc.contributor.scopusid6602927353tr_TR
dc.contributor.scopusid44661687400tr_TR
dc.contributor.scopusid7006269202tr_TR
dc.subject.scopusComplex; Palladium; 2-Phenylpyridineen_US
dc.subject.emtreeBis(2 pyridylmethyl)amineen_US
dc.subject.emtreeCaspase 3en_US
dc.subject.emtreeNicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferaseen_US
dc.subject.emtreePalladium complexen_US
dc.subject.emtreeSaccharinen_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBreast canceren_US
dc.subject.emtreeCancer cellen_US
dc.subject.emtreeCell deathen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug cytotoxicityen_US
dc.subject.emtreeDrug dosage form comparisonen_US
dc.subject.emtreeDrug synthesisen_US
dc.subject.emtreeFuorescence microscopyen_US
dc.subject.emtreeGene expressionen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIC 50en_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreePolymerase chain reactionen_US
dc.subject.emtreeWestern blottingen_US
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