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dc.contributor.authorHolien, Toril
dc.contributor.authorMisund, Kristine
dc.contributor.authorOlsen, Oddrun Elise
dc.contributor.authorBaranowska, Katarzyna Anna
dc.contributor.authorBuene, Glenn
dc.contributor.authorBørset, Magne
dc.contributor.authorWaage, Anders
dc.contributor.authorSundan, Anders
dc.date.accessioned2015-06-03T20:47:43Z
dc.date.accessioned2015-06-08T10:57:25Z
dc.date.available2015-06-03T20:47:43Z
dc.date.available2015-06-08T10:57:25Z
dc.date.issued2015
dc.identifier.citationOncoTarget 2015
dc.identifier.issn1949-2553
dc.identifier.issn1949-2553
dc.identifier.urihttp://hdl.handle.net/11250/284777
dc.description.abstractIn multiple myeloma, elevated MYC expression is related to disease initiation and progression. We found that in myeloma cell lines, MYC gene amplifications were common and correlated with MYC mRNA and protein. In primary cell samples MYC mRNA levels were also relatively high; however gene copy number alterations were uncommon. Elevated levels of MYC in primary myeloma cells have been reported to arise from complex genetic aberrations and are more common than previously thought. Thus, elevated MYC expression is achieved differently in myeloma cell lines and primary cells. Sensitivity of myeloma cell lines to the MYC inhibitor 10058-F4 correlated with MYC expression, supporting that the activity of 10058-F4 was through specific inhibition of MYC.
dc.language.isoeng
dc.titleMYC amplifications in myeloma cell lines; correlation with MYC-inhibitor efficacy
dc.typeJournal article
dc.typePeer revieweden_GB
dc.date.updated2015-06-03T20:47:42Z
dc.source.journalOncoTarget
dc.identifier.doi10.18632/oncotarget.4245
dc.identifier.cristin1246200
dc.description.localcodeCopyright @ 2008-2015 Impact Journals, LLC. All rights reserved. Impact Journals is a trademark of Impact Journals, LLC . All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.


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