4.5 Review

Targeting FLT3 kinase in acute myelogenous leukemia: Progress, perils, and prospects

Journal

MINI-REVIEWS IN MEDICINAL CHEMISTRY
Volume 4, Issue 3, Pages 255-271

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1389557043487394

Keywords

FLT3; tyrosine kinase; kinase inhibitor; AML; KIT; PDGFR

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Activating mutations of the FLT3 receptor tyrosine kinase are the most common recurring genetic abnormality in acute myelogenous leukemia (AM). Inhibition of FLT3 kinase activity by small molecule inhibitors has been proposed as a novel therapeutic approach AML. The pre-clinical and clinical development of candidate FLT3 inhibitors will be reviewed.

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