Title : Recurrent Mutations in Cyclin D3 Confer Clinical Resistance to FLT3 Inhibitors in Acute Myeloid Leukemia.

Pub. Date : 2021 Jul 15

PMID : 34103301






4 Functional Relationships(s)
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1 The purpose of this study is to identify co-occurring mutations that influence clinical response to the novel FLT3 inhibitor pexidartinib (PLX3397). pexidartinib fms related receptor tyrosine kinase 3 Homo sapiens
2 The purpose of this study is to identify co-occurring mutations that influence clinical response to the novel FLT3 inhibitor pexidartinib (PLX3397). pexidartinib fms related receptor tyrosine kinase 3 Homo sapiens
3 EXPERIMENTAL DESIGN: We performed targeted sequencing of pretreatment blasts from 29 patients with FLT3 internal tandem duplication (ITD) mutations treated on the phase I/II trial of pexidartinib in relapsed/refractory FLT3-ITD+ acute myeloid leukemia (AML). pexidartinib fms related receptor tyrosine kinase 3 Homo sapiens
4 Expression of the Q276* and T283A mutations in FLT3-ITD MV4;11 cells conferred resistance to apoptosis, decreased cell-cycle arrest, and increased proliferation in the presence of pexidartinib and other FLT3 inhibitors. pexidartinib fms related receptor tyrosine kinase 3 Homo sapiens