Dasatinib inhibits proliferation and induces apoptosis in the KASUMI-1 cell line bearing the t(8;21)(q22;q22) and the N822K c-kit mutation

Leuk Res. 2013 Feb;37(2):175-82. doi: 10.1016/j.leukres.2012.10.011. Epub 2012 Nov 10.

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.

MeSH terms

  • Apoptosis / drug effects*
  • Caspases / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chromosomes, Human, Pair 21
  • Chromosomes, Human, Pair 8
  • Dasatinib
  • Enzyme Activation / drug effects
  • Humans
  • K562 Cells
  • Leukemia, Myeloid, Acute / genetics
  • Mutation*
  • Phosphorylation / drug effects
  • Protein Isoforms
  • Protein Kinase Inhibitors / pharmacology*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins c-kit / genetics*
  • Pyrimidines / pharmacology*
  • Thiazoles / pharmacology*
  • Translocation, Genetic*
  • src-Family Kinases / antagonists & inhibitors

Substances

  • Protein Isoforms
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Thiazoles
  • Proto-Oncogene Proteins c-kit
  • src-Family Kinases
  • Proto-Oncogene Proteins c-akt
  • Caspases
  • Dasatinib