Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/32396
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dc.contributor.authorSamli, Murat-
dc.contributor.authorŞahin, Ahmet-
dc.date.accessioned2023-04-14T11:15:45Z-
dc.date.available2023-04-14T11:15:45Z-
dc.date.issued2019-06-
dc.identifier.citationŞamlı, H. vd. (2019). ''Paclitaxel resistance and the role of miRNAs in prostate cancer cell lines''. World Journal of Urology, 37(6), Special Issue, 1117-1126.en_US
dc.identifier.issn0724-4983-
dc.identifier.issn1433-8726-
dc.identifier.urihttps://doi.org/10.1007/s00345-018-2501-6-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00345-018-2501-6-
dc.identifier.urihttp://hdl.handle.net/11452/32396-
dc.description.abstractPurposeTo investigate the expression profiles of 86 miRNAs in paclitaxel-resistant prostate cancer cell lines and to identify the genes that have a role in the development of drug resistance.MethodsThree prostate cancer cell lines, androgen-dependent VCaP, androgen-independent PC-3 and DU-145, were used to obtain paclitaxel-resistant cells by progressively increasing the concentration of paclitaxel in the culture medium. Viability assays with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium and sulforhodamine B were used to assess the cell resistance level and cytotoxic effects of paclitaxel treatment. Total RNA was isolated from both prostate cancer cell lines and their resistant versions, and cDNA samples were reverse transcribed from total RNA. Selected target genes of miRNAs that showed differences in expression and were estimated to be effective on drug resistance mechanism were analyzed with western blot analysis.ResultsExpression study of 86 miRNAs by RT-PCR demonstrated that several of the miRNAs were expressed at different levels in paclitaxel-resistant cells compared to wild-type cells. Moreover, the expression profiles of these miRNAs varied among different prostate cancer cell line types, with 13 miRNAs being up-regulated in the resistant cells. Among these, miR-200b-3p, miR-34b-3p and miR-375 exhibited a marked up-regulation. Further, miR-100-5p showed a prominent increase in paclitaxel-resistant VCaP-R and DU145-R cells. Western blot and RT-PCR studies showed that only the LARP1 and CCND1 genes were over-expressed up to 2-5 times in all paclitaxel-resistant cell lines compared to the other investigated genes.ConclusionsIn this study, the three paclitaxel-resistant prostate cancer cell lines examined showed remarkably different miRNA expression profiles.en_US
dc.language.isoentr_TR
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectUrology & nephrologyen_US
dc.subjectMiRNAen_US
dc.subjectProstate canceren_US
dc.subjectPaclitaxelen_US
dc.subjectDrug resistanceen_US
dc.subjectMesenchymal Transitionen_US
dc.subjectSensitivityen_US
dc.subjectMicrornasen_US
dc.subjectExpressionen_US
dc.subjectRegulatoren_US
dc.subjectDocetaxelen_US
dc.subjectFamilyen_US
dc.subjectLarp1en_US
dc.subject.meshAntineoplastic Agents, Phytogenicen_US
dc.subject.meshCell Line, Tumoren_US
dc.subject.meshDrug Resistance, Neoplasmen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMicroRNAsen_US
dc.subject.meshPaclitaxelen_US
dc.subject.meshProstatic Neoplasmsen_US
dc.titlePaclitaxel resistance and the role of miRNAs in prostate cancer cell linesen_US
dc.typeArticleen_US
dc.identifier.wos000468914100017tr_TR
dc.identifier.scopus2-s2.0-85053695511tr_TR
dc.relation.tubitak213S012tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Veteriner Fakültesi/Zootekni ve Hayvan Besleme/Veterinerlik Genetiği Bölümü.tr_TR
dc.contributor.orcid0000-0003-2758-5945tr_TR
dc.contributor.orcid0000-0003-3118-8061tr_TR
dc.identifier.startpage1117tr_TR
dc.identifier.endpage1126tr_TR
dc.identifier.volume37tr_TR
dc.identifier.issue6, Special Issueen_US
dc.relation.journalWorld Journal of Urologyen_US
dc.contributor.buuauthorSamlı, Hale-
dc.contributor.buuauthorVatansever, Buse-
dc.contributor.buuauthorArdıçlı, Sena-
dc.contributor.buuauthorAztopal, Nazlıhan-
dc.contributor.buuauthorDincel, Deniz-
dc.contributor.buuauthorBalcı, Faruk-
dc.contributor.researcheridAAH-6488-2021tr_TR
dc.contributor.researcheridAAM-4361-2020tr_TR
dc.contributor.researcheridAAH-6192-2021tr_TR
dc.contributor.researcheridL-6687-2018tr_TR
dc.contributor.researcheridAAV-4886-2020tr_TR
dc.contributor.researcheridO-3394-2019tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed30244336tr_TR
dc.subject.wosUrology & nephrologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid6507670789tr_TR
dc.contributor.scopusid57203938885tr_TR
dc.contributor.scopusid56607305700tr_TR
dc.contributor.scopusid55853882900tr_TR
dc.contributor.scopusid56607385000tr_TR
dc.contributor.scopusid16062981700tr_TR
dc.subject.scopusUrinary Bladder Neoplasms; Prostatic Neoplasms; Micrornaen_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeMicroRNAen_US
dc.subject.emtreePaclitaxelen_US
dc.subject.emtreeDrug resistanceen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeProstate tumoren_US
dc.subject.emtreeTumor cell lineen_US
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