Schiff Base-Poloxamer P85 Combination Prevents Prostate Cancer Progression in C57/Bl6 Mice

dc.contributor.authorDogan, Aysegul
dc.contributor.authorDemirci, Selami
dc.contributor.authorTurkmen, Nese Basak
dc.contributor.authorCaglayan, Ahmet Burak
dc.contributor.authorAydin, Safa
dc.contributor.authorTelci, Dilek
dc.contributor.authorSahin, Fikrettin
dc.date.accessioned2026-08-12T17:32:55Z
dc.date.issued2016
dc.departmentFırat Üniversitesi
dc.description.abstractBACKGROUNDProstate cancer which is the second most common cause of death among men has a high incidence in recent years. Current therapeutic regimens should be improved to overcome drug resistance. At the metastatic stage, tumors become refractory to established chemotherapeutic treatments and cause serious problems at the clinics. Development of new drug molecules that are able to transport through the membrane easily and kill tumor cells rapidly is of great interest. METHODIn the current study, a novel Heterodinuclear copper(II)Mn(II) Schiff base complex combined with P85 was used for prostate cancer treatment in vivo. Tramp-C1 cells injected animals were subjected to chemotherapeutic formulation treatment and results were analyzed by toxicology analysis, tumor volume measurements, and histopathological analysis. 0.5mg/kg Schiff base was selected and combined with 0.05% P85 according to the toxicology analysis showing the enzyme levels, blood parameters, and multiple organ toxicity. RESULTSResults demonstrated that Heterodinuclear copper(II)Mn(II) complex-P85 combination decreased tumor formation and tumor volume steadily over the course of experiments. CONCLUSIONSOverall, Heterodinuclear copper(II)Mn(II) complex-P85 exerted remarkable anti-cancer activity in vivo in C57/B16 mice. Prostate 76:1454-1463, 2016. (c) 2016 Wiley Periodicals, Inc.
dc.identifier.doi10.1002/pros.23229
dc.identifier.endpage1463
dc.identifier.issn0270-4137
dc.identifier.issn1097-0045
dc.identifier.issue15
dc.identifier.orcid0000-0001-9542-5244
dc.identifier.orcid0000-0003-4138-7689
dc.identifier.orcid0000-0001-6494-8923
dc.identifier.orcid0000-0002-6174-1609
dc.identifier.orcid0000-0002-1329-3143
dc.identifier.orcid0000-0002-2793-6533
dc.identifier.orcid0000-0002-6242-3709
dc.identifier.pmid27338565
dc.identifier.scopus2-s2.0-84977534680
dc.identifier.scopusqualityQ1
dc.identifier.startpage1454
dc.identifier.urihttps://doi.org/10.1002/pros.23229
dc.identifier.urihttps://hdl.handle.net/11508/56825
dc.identifier.volume76
dc.identifier.wosWOS:000384547100011
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofProstate
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectSchiff base
dc.subjectpluronic
dc.subjectP85
dc.subjectprostate cancer
dc.subjecttramp-C1
dc.titleSchiff Base-Poloxamer P85 Combination Prevents Prostate Cancer Progression in C57/Bl6 Mice
dc.typeArticle

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