Potent efficacy of chlorpromazine in acute myeloid leukemia harboring KIT-D816V mutation
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Updated: Oct 31, 2025

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
Shinya Rai1, Hirokazu Tanaka1, J Luis Espinoza1
1Department of Hematology and Rheumatology, Kindai University Faculty of Medicine, Osaka-sayama, Osaka.
Abstract:
Acute myeloid leukemia (AML) is a heterogeneous disease often associated with poor prognosis. We previously showed that the localization of KIT-D816V at endolysosomes is critical to activate aberrant Akt signaling and Chlorpromazine (CPZ) perturbs the intracellular localization, leading to cell death in AML cells with KIT-D816V. We report that daily administration of CPZ, prescribed for controlling anxiety disorder in patient with AML harboring KIT-D816V, led to a dramatic reduction in AML cells. In vitro and in vivo experiments showed that CPZ inhibited the growth and survival of the patient-derived AML cells, implying potent efficacy of CPZ in AML with KIT-D816V.
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