Targeting ABL and SRC kinases in chronic myeloid leukemia: experience with dasatinib.

Abstract

Mutations within the ABL kinase domain and overexpression of SRC family kinases have been identified among the known mechanisms of resistance to imatinib in chronic myeloid leukemia (CML). The development of agents with dual inhibitory activity against SRC and ABL kinases is one approach to overcome imatinib resistance. One such agent, dasatinib (formerly BMS-354825), is approximately 300-fold more potent against BCR-ABL than imatinib, and is active against all tested ABL mutant isoforms, except for T315I. Dasatinib has demonstrated high efficacy in Phase I and II studies in patients with CML following failure of imatinib therapy. Studies exploring the efficacy of dasatinib as front-line therapy in patients with BCR-ABL-expressing hematologic malignancies are underway.

• Authors: Alfonso Quintás-Cardama, Hagop Kantarjian, Jorge Cortes
• Journal: Future oncology (London, England) (Future Oncol) Vol. 2 Issue 6 Pg. 655-65 (Dec 2006) ISSN: 1479-6694 [Print] England
• PMID: 17155893 (Publication Type: Journal Article, Review)

Chemical References

• Benzamides
• Piperazines
• Protein Kinase Inhibitors
• Pyrimidines
• Thiazoles
• Imatinib Mesylate
• Fusion Proteins, bcr-abl
• src-Family Kinases
• Dasatinib

Topics

• Benzamides
• Dasatinib
• Drug Resistance, Neoplasm
• Fusion Proteins, bcr-abl (drug effects)
• Humans
• Imatinib Mesylate
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive (drug therapy)
• Piperazines (pharmacology)
• Protein Kinase Inhibitors (pharmacology, therapeutic use)
• Pyrimidines (pharmacology, therapeutic use)
• Thiazoles (pharmacology, therapeutic use)
• src-Family Kinases (drug effects)