Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.25835
Title: LEE011 and ruxolitinib: A synergistic drug combination for natural killer/T-cell lymphoma (NKTCL)
Authors: Hee, Y.T
Yan, J 
Nizetic, D
Chng, W.-J 
Keywords: cyclin dependent kinase 4
cyclin dependent kinase 6
Janus kinase 1
Janus kinase 2
ribociclib
ruxolitinib
STAT protein
Article
cancer combination chemotherapy
cancer inhibition
cell cycle progression
cell viability
controlled study
drug efficacy
drug potentiation
drug targeting
enzyme inhibition
IC50
lymphoma cell line
monotherapy
NK T cell lymphoma
Issue Date: 2018
Citation: Hee, 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
Rights: Attribution 4.0 International
Abstract: Natural 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.
Source Title: Oncotarget
URI: https://scholarbank.nus.edu.sg/handle/10635/178073
ISSN: 19492553
DOI: 10.18632/oncotarget.25835
Rights: Attribution 4.0 International
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