Mir-17 in Imatinib Resistance and Response To Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia Cells
| dc.contributor.author | Fıratlıgil, Burcu | |
| dc.contributor.author | Biray Avcı, Çığır | |
| dc.contributor.author | Baran, Yusuf | |
| dc.date.accessioned | 2017-04-12T13:42:26Z | |
| dc.date.available | 2017-04-12T13:42:26Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | In this study we examined the expression levels of miR-17 which possesses oncogenic activities through downregulation of CDKN1A, p21 and E2F1 tumor suppressor genes, in imatinib sensitive and resistant chronic myeloid leukemia (CML) cells. On the other hand, we also determined the expression levels of miR-17 in response to tyrosine kinase inhibitors imatinib, nilotinib and dasatinib used for the treatment of CML. Methods: The expression profiles of miR-17 were analysed by Stem-Loop reverse transcription (RT) polymerase chain reaction (PCR). Results: The results revealed significant increase in the expression levels of miR-17 in imatinib sensitive and resistant cells compared to peripheral blood mononuclear cells (PBMCs). On the other hand, significant decrease was observed in miR-17 levels in response to imatinib, nilotinib and dasatinib. Conclusion: These results may imply that miR-17 can be used for diagnosis and treatment of CML. | en_US |
| dc.description.sponsorship | Scientific and Technological Research Council of Turkey | en_US |
| dc.identifier.citation | Fıratlıgil, B., Biray Avcı, Ç., and Baran, Y. (2013). miR-17 in imatinib resistance and response to tyrosine kinase inhibitors in chronic myeloid leukemia cells. Journal of B.U.ON., 18(2), 437-441. | en_US |
| dc.identifier.issn | 1107-0625 | |
| dc.identifier.scopus | 2-s2.0-84879578050 | |
| dc.identifier.uri | https://hdl.handle.net/11147/5295 | |
| dc.language.iso | en | en_US |
| dc.publisher | Zerbinis Medical Publications | en_US |
| dc.relation.ispartof | Journal of B.U.ON. | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Chronic myeloid leukemia | en_US |
| dc.subject | Dasatinib | en_US |
| dc.subject | Drug resistance | en_US |
| dc.subject | Imatinib | en_US |
| dc.subject | MicroRNAs | en_US |
| dc.subject | Nilotinib | en_US |
| dc.title | Mir-17 in Imatinib Resistance and Response To Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia Cells | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.institutional | Fıratlıgil, Burcu | |
| gdc.author.institutional | Baran, Yusuf | |
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| gdc.description.department | İzmir Institute of Technology. Molecular Biology and Genetics | en_US |
| gdc.description.endpage | 441 | en_US |
| gdc.description.issue | 2 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
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| gdc.description.startpage | 437 | en_US |
| gdc.description.volume | 18 | en_US |
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| gdc.identifier.pmid | 23818358 | |
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| gdc.oaire.keywords | Dasatinib | |
| gdc.oaire.keywords | Antineoplastic Agents | |
| gdc.oaire.keywords | Real-Time Polymerase Chain Reaction | |
| gdc.oaire.keywords | Piperazines | |
| gdc.oaire.keywords | chronic myeloid leukemia | |
| gdc.oaire.keywords | Leukemia, Myelogenous, Chronic, BCR-ABL Positive | |
| gdc.oaire.keywords | Humans | |
| gdc.oaire.keywords | dasatinib | |
| gdc.oaire.keywords | Molecular Targeted Therapy | |
| gdc.oaire.keywords | Protein Kinase Inhibitors | |
| gdc.oaire.keywords | nilotinib | |
| gdc.oaire.keywords | drug resistance | |
| gdc.oaire.keywords | miR-17 | |
| gdc.oaire.keywords | Reverse Transcriptase Polymerase Chain Reaction | |
| gdc.oaire.keywords | Chronic myeloid leukemia | |
| gdc.oaire.keywords | Protein-Tyrosine Kinases | |
| gdc.oaire.keywords | Nilotinib | |
| gdc.oaire.keywords | Gene Expression Regulation, Neoplastic | |
| gdc.oaire.keywords | MicroRNAs | |
| gdc.oaire.keywords | Thiazoles | |
| gdc.oaire.keywords | Pyrimidines | |
| gdc.oaire.keywords | imatinib | |
| gdc.oaire.keywords | Drug Resistance, Neoplasm | |
| gdc.oaire.keywords | Drug resistance | |
| gdc.oaire.keywords | Imatinib | |
| gdc.oaire.keywords | Benzamides | |
| gdc.oaire.keywords | Imatinib Mesylate | |
| gdc.oaire.keywords | K562 Cells | |
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