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dc.contributor.authorSuat, Tekin
dc.contributor.authorYavuz, Erden
dc.contributor.authorSuleyman, Sandal
dc.contributor.authorBayram, Yilmaz
dc.date.accessioned2019-08-09T06:14:28Z
dc.date.available2019-08-09T06:14:28Z
dc.date.issued2018
dc.identifier.citationTekin, S., Erden, Y., Sandal, S., Yilmaz, B. (2015). Is irisin an anticarcinogenic peptide. Medicine Science, 4(2), 2172-2180.en_US
dc.identifier.urihttp://www.scopemed.org/?mno=171454
dc.identifier.urihttp://hdl.handle.net/11772/1754
dc.description.abstractIrisin is thought an anti obesity hormone, which regulates body weight and metabolism, including insulin resistance. It is known that obesity is a risk factor in the development of cancer. This study was designed to evaluate whether there is a role of irisin on viability of human prostate cancer cells. In the present study, 0.1, 1, 10 and 100 nM concentrations of irisin were applied to human prostate cancer cells with androgen receptor positive (LNCaP) and androgen receptor negative (DU-145, PC3). Effects of irisin were determined using 3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. At the end of study, all concentrations of irisin reduced viability in the three types of prostate cells, but only 10 and 100 nM concentrations of the irisin caused a significant decreases (p<0.05). Consequently, high concentrations of irisin in both androgen receptor positive and androgen receptor negative cell lines reduced cell viability. These results show that the cytotoxic effects of irisin on prostate cancer cells are not dependent on androgen receptor mechanism.en_US
dc.language.isoengen_US
dc.publisherMedicine Scienceen_US
dc.relation.isversionof10.5455/medscience.2014.03.8210en_US
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_US
dc.subjectIrisinen_US
dc.subjectLNCaPen_US
dc.subjectDU-145en_US
dc.subjectCell viabilityen_US
dc.titleIs irisin an anticarcinogenic peptide?en_US
dc.typearticleen_US
dc.relation.journalMedicine Scienceen_US
dc.contributor.departmentBartın Üniversitesi, Fen Fakültesi, Moleküler Biyoloji ve Genetik Bölümüen_US
dc.identifier.volume4en_US
dc.identifier.issue2en_US
dc.identifier.startpage2172en_US
dc.identifier.endpage2180en_US


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