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dc.contributor.authorGenc, Gurkan
dc.contributor.authorKilinc, Veli
dc.contributor.authorBedir, Abdulkerim
dc.contributor.authorOzkaya, Ozan
dc.date.accessioned2020-06-21T13:56:53Z
dc.date.available2020-06-21T13:56:53Z
dc.date.issued2014
dc.identifier.issn0886-022X
dc.identifier.issn1525-6049
dc.identifier.urihttps://doi.org/10.3109/0886022X.2014.926755
dc.identifier.urihttps://hdl.handle.net/20.500.12712/15055
dc.descriptionozkaya, ozan/0000-0002-0198-1221en_US
dc.descriptionWOS: 000340259600019en_US
dc.descriptionPubMed: 24937012en_US
dc.description.abstractCisplatin is a chemotherapeutic agent, which is used in the treatment of various solid organ cancers, and its main dose limiting side effect of cisplatin is nephrotoxicity. The aim of this study is to investigate the role of pioglitazone and creatine on cisplatin nephrotoxicity in vitro. Real-time cell analyzer system (RTCA) was used for real-time and time-dependent analysis of the cellular response of HK-2 cells following incubation with cisplatin and combination with creatine or pioglitazone hydrochloride. First, half-maximal inhibitory concentrations (IC50) of cisplatin, creatine and pioglitazone were calculated by RTCA system. Afterwards creatine and pioglitazone was administered with serial dilutions under RTCA system. IC50 dose for cisplatin was 7.69M x 10(-5) at 24th hour and 3.93M x 10(-6) at 48th hour. IC50 dose for pioglitazone was 1.61M x 10(-3) at 24th hour and 2.85M x 10(-4) at 48th hour. Although cells were treated the dose of 40,225mM creatine, IC50 dose could not been reached. Neither pioglitazone nor creatine had additional protective effect in any dose. Consequently, beneficial effect of creatine and pioglitazone on cisplatin-induced cell death could not be found. Further studies and clinical trials are needed to evaluate the effect of different doses of these drugs in cisplatin-induced nephrotoxicity.en_US
dc.description.sponsorshipOndokuz Mayis UniversityOndokuz Mayis University [PYO.TIP.1901.10.014]en_US
dc.description.sponsorshipThe authors report no declarations of interest. This study was supported by grants from the Ondokuz Mayis University Research Fund with the number PYO.TIP.1901.10.014en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.3109/0886022X.2014.926755en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDrug toxicityen_US
dc.subjectcisplatinen_US
dc.subjectcreatineen_US
dc.subjectpioglitazoneen_US
dc.titleEffect of creatine and pioglitazone on Hk-2 cell line cisplatin nephrotoxicityen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume36en_US
dc.identifier.issue7en_US
dc.identifier.startpage1104en_US
dc.identifier.endpage1107en_US
dc.relation.journalRenal Failureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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