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dc.contributor.authorHee, YTen_US
dc.contributor.authorYan, Jen_US
dc.contributor.authorNizetic, Den_US
dc.contributor.authorChng, W-Jen_US
dc.date.accessioned2020-01-23T13:04:26Z
dc.date.available2018-07-12en_US
dc.date.issued2018-08-07en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/62508
dc.description.abstractNatural killer/T-cell lymphoma (NKTCL) is an aggressive non-Hodgkin lymphoma that has been facing limited success with conventional treatments, urging for the discovery of alternative strategies. Recent studies including ours have revealed that EZH2 and JAK-STAT signalling pathways are key contributors to NKTCL pathogenesis. In particular, we found that EZH2 is overexpressed and directly transcriptionally activates the CCND1 gene to confer growth advantage. CCND1 codes for cyclin D1, which complexes with CDK4/6 to promote G1 to S phase transition. Therefore in this study we investigated whether inhibiting both JAK1/2 and CDK4/6, using LEE011 and ruxolitinib respectively is effective in NKTL. We first demonstrate that separate LEE011 and ruxolitinib treatment is sufficient to cause growth inhibition of NKTCL cells. More importantly, we found that there is synergistic growth inhibitory effects on NKTCL cells with combination treatment of LEE011 and ruxolitinib. The results obtained shows that the targeting of both CDK4/6 and JAK1/2 are promising to develop better treatment alternatives for NKTCL.en_US
dc.description.sponsorshipThis study was supported by the National Medical Research Council (NMRC) grants NMRC/Clinician Scientist-Individual Research/1343/2012 (WJC), NMRC/Basic Research Grant-New Investigator/2021/2014 (JY) and the Singapore Ministry of Education Academic Research Fund Tier 2 grant MOE2015-T2-2-119 (DN). WJC was also supported by the NMRC Clinician Scientist Investigator Award.en_US
dc.format.extent31832 - 31841en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofOncotargeten_US
dc.rightsCreative Commons Attribution
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectLEE011en_US
dc.subjectNKTCLen_US
dc.subjectdrug combinationen_US
dc.subjectlymphomaen_US
dc.subjectruxolitiniben_US
dc.titleLEE011 and ruxolitinib: a synergistic drug combination for natural killer/T-cell lymphoma (NKTCL).en_US
dc.typeArticle
dc.rights.holder2018 Hee et al.
dc.identifier.doi10.18632/oncotarget.25835en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/30159126en_US
pubs.issue61en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume9en_US
dcterms.dateAccepted2018-07-12en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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