Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/38195
Title: Pro-survival signal inhibition by CDK inhibitor dinaciclib in Chronic Lymphocytic Leukaemia
Authors: Chen, Yixiang
Germano, Sandra
Clements, Chris
Samuel, Jesvin
Shelmani, Ghalia
Jayne, Sandrine
Dyer, Martin J. S.
Macip, Salvador
First Published: 29-Jul-2016
Publisher: Wiley
Citation: British Journal of Haematology, 2016, doi: 10.1111/bjh.14285
Abstract: Dinaciclib is a cyclin-dependent kinase inhibitor with clinical potential in different cancers, including chronic lymphocytic leukaemia (CLL). In order to better understand its cytotoxic action, we characterized its effects on signalling pathways important for the survival of CLL cells. We found that dinaciclib induced apoptosis through the activation of caspases 8 and 9, which was independent of the presence of cytokines to mimic the environment of proliferation centres or IGVH mutation status. Moreover, treatment with dinaciclib led to the inhibition of oncogenic pathways normally activated in stimulated CLL cells, such as STAT3, NF-κB, p38, PI3K/AKT and RAF/MEK/ERK. Dinaciclib was also able to block the expression of anti-apoptotic proteins of the BCL2 family such as MCL1 and BCL-xL (also termed BCL2L1). Finally, we showed that low concentrations of dinaciclib enhanced cell sensitivity to ibrutinib and the BCL2 inhibitor ABT-199, two drugs with known effects on CLL. Taken together, our data show that dinaciclib targets multiple pro-survival signalling pathways in CLL, which provides a mechanistic explanation for its potent induction of apoptosis. They also support a therapeutic application of cyclin-dependent kinase inhibitors in CLL in combination with other relevant targeted therapies.
DOI Link: 10.1111/bjh.14285
ISSN: 0007-1048
eISSN: 1365-2141
Links: http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14285/full
http://hdl.handle.net/2381/38195
Embargo on file until: 29-Jul-2017
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © Wiley, 2016. This version of the article is distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Appears in Collections:Published Articles, Dept. of Molecular and Cell Biology

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