Transitory dasatinib-resistant states in KIT(mut) t(8;21) acute myeloid leukemia cells correlate with altered KIT expression

Item Type:	Article
Title:	Transitory dasatinib-resistant states in KIT(mut) t(8;21) acute myeloid leukemia cells correlate with altered KIT expression
Creators Name:	Herrmann, M.D. and Lennerz, J.K. and Bullinger, L. and Bartholomae, S. and Holzmann, K. and Westhoff, M.A. and Corbacioglu, S. and Debatin, K.M.
Abstract:	KIT inhibition with dasatinib represents a promising approach to targeted therapy in t(8;21) acute myeloid leukemia (AML) and clinical trials are currently evaluating its clinical relevance. However, data on continuous long-term dasatinib exposure of AML cells are limited and the potential effects on KIT inhibition and dasatinib sensitivity are unexplored. Treatment-related resistance ultimately limits clinical efficacy of tyrosine kinase inhibitors (TKI), which could similarly apply to dasatinib in t(8;21) AML. In this study, we used the dasatinib-sensitive KIT(mut) t(8;21) AML cell line Kasumi-1 to model, in a confined and controllable way, molecular effects upon continuous dasatinib treatment. Long-term dasatinib exposure at clinically relevant levels resulted in markedly decreased drug-sensitivity of KIT(mut) t(8;21) AML cells. Notably, all dasatinib-resistant clones lacked secondary KIT-mutations. Instead, persistent growth correlated with alterations in KIT expression levels-that is, either KIT overexpression with maintained downstream signaling or KIT downregulation with concomitant activation of alternate pathways. Although KIT overexpression was associated with retained receptor activity and STAT3 activation, KIT downregulation correlated with decreased STAT3 levels and increased ERK-signaling. Importantly, brief discontinuation of dasatinib restored dasatinib-sensitivity associated with reversal of signaling signatures similar to treatment-naive, dasatinib-sensitive cells. The observed desensitization of KIT(mut) t(8;21) AML cells upon continuous dasatinib exposure suggests that therapy-related acquisition of resistance could pose significant limitations on therapeutic efficiency. Notably, we identified TKI-resistant states of transient nature that correlate with alterations in KIT expression and can be reversed upon brief inhibitor withdrawal. These findings indicate that discontinuing treatment maintains dasatinib sensitivity in KIT(mut) AML cells.
Keywords:	Acute Myeloid Leukemia, Antineoplastic Agents, Apoptosis, Cell Proliferation, Dasatinib, Gene Expression Profiling, Genetic Translocation, Neoplasm Drug Resistance, Mutation, Pair 21 Human Chromosomes, Pair 8 Human Chromosomes, Proto-Oncogene Proteins c-kit, Pyrimidines, Thiazoles
Source:	Experimental Hematology
ISSN:	0301-472X
Publisher:	Elsevier
Volume:	42
Number:	2
Page Range:	90-100
Date:	February 2014
Official Publication:	https://doi.org/10.1016/j.exphem.2013.10.006
PubMed:	View item in PubMed

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