RNAi-induced down-regulation of FLT3 expression in AML cell lines increases sensitivity to MLN518.

Abstract

FMS-like tyrosine kinase 3 (FLT3) is a receptor tyrosine kinase that is constitutively activated in approximately 30% of acute myelogenous leukemia (AML) patients and appears to confer an adverse prognosis. Thus, development of inhibitors and/or antibodies that specifically target FLT3 has been of substantial interest. In this regard, phase 1 and 2 trials involving FLT3 inhibitors have recently reported FLT3 inhibition and leukemic blast reduction in some patients. Despite this, issues such as specificity and resistance need to be addressed. Consequently, the development of alternative approaches for targeting FLT3 would be of great consequence. In the present report, we demonstrate that FLT3 siRNA effectively down-regulates FLT3 expression in Ba/F3 cells transfected with FLT3 containing an activating internal tandem duplication (ITD) in the juxtamembrane domain and FLT3-ITD-positive Molm-14 human leukemia cells. Treatment with the FLT3 siRNA results in growth inhibition and apoptosis of these cells. Furthermore, siRNA-induced down-regulation of FLT3 increased the sensitivity of both cell lines to treatment with the FLT3 inhibitor MLN518. This illustrates the potential benefit of combined therapeutic approaches.

• Authors: Denise K Walters, Eric P Stoffregen, Michael C Heinrich, Michael W Deininger, Brian J Druker
• Journal: Blood (Blood) Vol. 105 Issue 7 Pg. 2952-4 (Apr 01 2005) ISSN: 0006-4971 [Print] United States
• PMID: 15585651 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Piperazines
• Protein Kinase Inhibitors
• Proto-Oncogene Proteins
• Quinazolines
• RNA, Small Interfering
• tandutinib
• FLT3 protein, human
• Receptor Protein-Tyrosine Kinases
• fms-Like Tyrosine Kinase 3

Topics

• Cell Line, Tumor
• Down-Regulation
• Drug Resistance, Neoplasm
• Humans
• Leukemia, Myeloid, Acute (drug therapy, physiopathology)
• Piperazines (pharmacology)
• Protein Kinase Inhibitors (pharmacology)
• Proto-Oncogene Proteins (antagonists & inhibitors, genetics)
• Quinazolines (pharmacology)
• RNA, Small Interfering (pharmacology)
• Receptor Protein-Tyrosine Kinases (antagonists & inhibitors, genetics)
• Transfection
• fms-Like Tyrosine Kinase 3