Title : Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia.

Pub. Date : 2012 Apr 15

PMID : 22504184






1 Functional Relationships(s)
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1 Here we report point mutations at three residues within the kinase domain of FLT3-ITD that confer substantial in vitro resistance to AC220 (quizartinib), an active investigational inhibitor of FLT3, KIT, PDGFRA, PDGFRB and RET; evolution of AC220-resistant substitutions at two of these amino acid positions was observed in eight of eight FLT3-ITD-positive AML patients with acquired resistance to AC220. quizartinib ret proto-oncogene Homo sapiens