| Literature DB >> 23149070 |
Vassiliki E Mpakou1, Frieda Kontsioti, Sotiris Papageorgiou, Aris Spathis, Christine Kottaridi, Kostas Girkas, Petros Karakitsos, George Dimitriadis, Ioannis Dervenoulas, Vasiliki Pappa.
Abstract
Activating mutations of the c-kit gene are frequently found in CBF (core binding factor) leukemias. We evaluated the effect of tyrosine kinase inhibitor dasatinib in leukemic cell lines bearing or not c-kit mutations. Our data demonstrate that in the AML Kasumi-1 cell line, bearing the N822K c-kit mutation, dasatinib is a potent suppressor of c-kit and Src kinase activity and inhibits the phosphorylation of their downstream target AKT, possibly through the Src-mediated VEGF/VEGFR receptor type 2 pathway. Dasatinib also effectively blocks proliferation and induces apoptosis through caspase-3 activation in Kasumi-1 cells. These data further encourage the integration of dasatinib in the treatment of CBF AML with c-kit mutations in the context of clinical trials, which are eagerly anticipated.Entities:
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Year: 2012 PMID: 23149070 DOI: 10.1016/j.leukres.2012.10.011
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156