Author/Authors :
Corrado، نويسنده , , Chiara and Raimondo، نويسنده , , Stefania and Flugy، نويسنده , , Anna Maria and Fontana، نويسنده , , Simona and Santoro، نويسنده , , Alessandra and Stassi، نويسنده , , Giorgio and Marfia، نويسنده , , Anna and Iovino، نويسنده , , Flora and Arlinghaus، نويسنده , , Ralph and Kohn، نويسنده , , Elise C. and Leo، نويسنده , , Giacomo De and Alessandro، نويسنده , , Riccardo، نويسنده ,
Abstract :
Mutation of the Bcr–Abl oncoprotein is one of most frequent mechanisms by which chronic myelogenous leukemia (CML) cells become resistant to imatinib. Here, we show that treatment of cell lines harbouring wild type or mutant BCR–ABL with carboxyamidotriazole (CAI), a calcium influx and signal transduction inhibitor, inhibits cell growth, the expression of Bcr–Abl and its downstream signalling, and induces apoptosis. Moreover, we show that CAI acts by increasing intracellular ROS. Clinically significant, CAI has also inhibitory effects on T315I Bcr–Abl mutant, a mutation that causes CML cells to become insensitive to imatinib and second generation abl kinase inhibitors.
Keywords :
Chronic myelogenous leukemia (CML) , Carboxyamidotriazole (CAI) , Drug resistance , Reactive-oxygen species (ROS)