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
gdc.author.yokid 119193
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
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
gdc.description.scopusquality N/A
gdc.description.startpage 437 en_US
gdc.description.volume 18 en_US
gdc.identifier.openalex W2185879025
gdc.identifier.pmid 23818358
gdc.identifier.wos WOS:000322750700020
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype GOLD
gdc.oaire.diamondjournal false
gdc.oaire.downloads 5
gdc.oaire.impulse 4.0
gdc.oaire.influence 2.7402625E-9
gdc.oaire.isgreen true
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
gdc.oaire.popularity 1.7619836E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 0302 clinical medicine
gdc.oaire.views 3
gdc.openalex.collaboration National
gdc.openalex.fwci 0.61767124
gdc.openalex.normalizedpercentile 0.72
gdc.opencitations.count 7
gdc.plumx.mendeley 18
gdc.plumx.pubmedcites 3
gdc.plumx.scopuscites 8
gdc.scopus.citedcount 8
gdc.wos.citedcount 7
relation.isAuthorOfPublication.latestForDiscovery 7bb863bb-9384-4a07-9fbb-b9c1ab7634a3
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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