Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.25835
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dc.titleLEE011 and ruxolitinib: A synergistic drug combination for natural killer/T-cell lymphoma (NKTCL)
dc.contributor.authorHee, Y.T
dc.contributor.authorYan, J
dc.contributor.authorNizetic, D
dc.contributor.authorChng, W.-J
dc.date.accessioned2020-10-20T05:00:52Z
dc.date.available2020-10-20T05:00:52Z
dc.date.issued2018
dc.identifier.citationHee, Y.T, Yan, J, Nizetic, D, Chng, W.-J (2018). LEE011 and ruxolitinib: A synergistic drug combination for natural killer/T-cell lymphoma (NKTCL). Oncotarget 9 (61) : 31832-31841. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.25835
dc.identifier.issn19492553
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178073
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. © Hee et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcyclin dependent kinase 4
dc.subjectcyclin dependent kinase 6
dc.subjectJanus kinase 1
dc.subjectJanus kinase 2
dc.subjectribociclib
dc.subjectruxolitinib
dc.subjectSTAT protein
dc.subjectArticle
dc.subjectcancer combination chemotherapy
dc.subjectcancer inhibition
dc.subjectcell cycle progression
dc.subjectcell viability
dc.subjectcontrolled study
dc.subjectdrug efficacy
dc.subjectdrug potentiation
dc.subjectdrug targeting
dc.subjectenzyme inhibition
dc.subjectIC50
dc.subjectlymphoma cell line
dc.subjectmonotherapy
dc.subjectNK T cell lymphoma
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentMEDICINE
dc.description.doi10.18632/oncotarget.25835
dc.description.sourcetitleOncotarget
dc.description.volume9
dc.description.issue61
dc.description.page31832-31841
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