Neutralization of KIT oncogenic signaling in leukemia with antibodies targeting KIT membrane proximal domain 5
Menée sur des lignées cellulaires de leucémie, cette étude met en évidence des mécanismes par lesquels des anticorps spécifiques d'un domaine membranaire de KIT permettent de surmonter une résistance thérapeutique aux inhibiteurs de tyrosine kinase
KIT is a cell surface tyrosine kinase receptor whose ligand SCF (Stem Cell Factor) triggers homodimerization and activation of downstream effector pathways involved in cell survival, proliferation, homing or differentiation. KIT activating mutations are major oncogenic drivers in subsets of acute myeloid leukemia (AML), in mast cell leukemia and in gastrointestinal stromal tumors (GIST). The overexpression of SCF and/or wild type (WT) KIT is also observed in a number of cancers including 50% of AML and small cell lung cancer. The use of tyrosine kinase inhibitors (TKI) in these pathologies is however hampered by initial or acquired resistance following treatment. Using antibody phage display, we obtained 2 antibodies (2D1 and 3G1) specific for the most membrane proximal extracellular immunoglobulin domain (D5) of KIT which is implicated in KIT homodimerization. Produced as single chain variable antibody fragments fused to the Fc fragment of a human IgG1, bivalent 2D1-Fc and 3G1-Fc inhibited KIT-dependent growth of leukemic cell lines expressing WT KIT (UT7/Epo) or constitutively active KIT mutants including the TKI imatinib resistant KIT D816V mutant (HMC1.2 cell line). In all models, either expressing WT KIT or mutated KIT, 2D1 and 3G1-Fc induced KIT internalization and sustained surface down regulation. However, interestingly, KIT degradation was only observed in leukemic cell lines with oncogenic KIT, a property likely to limit the toxicity of these antibodies in patients. These fully human antibody formats may represent therapeutic tools to target KIT signaling in leukemia or GIST, and to bypass TKI resistance of certain KIT mutants.
http://mct.aacrjournals.org/content/early/2015/09/10/1535-7163.MCT-15-0321.abstract 2015