FLT3-ITD and tyrosine kinase domain mutants induce 2 distinct phenotypes in a murine bone marrow transplantation model

R Grundler, C Miething, C Thiede, C Peschel, J Duyster - Blood, 2005 - ashpublications.org
R Grundler, C Miething, C Thiede, C Peschel, J Duyster
Blood, 2005ashpublications.org
Activating mutations of the Fms-like tyrosine kinase 3 (FLT3) receptor are the most common
genetic alteration in acute myeloid leukemia (AML). Two distinct groups of FLT3 mutations
are found: internal tandem duplications (ITDs) of the juxtamembrane region and point
mutations within the tyrosine kinase domain (TKD). Recently, point mutations within the
activation loop of FLT3 have also been described in childhood acute lymphoblastic
leukemia (ALL). FLT3-ITD has been shown to induce a myeloproliferative syndrome in a …
Abstract
Activating mutations of the Fms-like tyrosine kinase 3 (FLT3) receptor are the most common genetic alteration in acute myeloid leukemia (AML). Two distinct groups of FLT3 mutations are found: internal tandem duplications (ITDs) of the juxtamembrane region and point mutations within the tyrosine kinase domain (TKD). Recently, point mutations within the activation loop of FLT3 have also been described in childhood acute lymphoblastic leukemia (ALL). FLT3-ITD has been shown to induce a myeloproliferative syndrome in a murine bone marrow transplantation model. The phenotype of FLT3-TKD in mice has not yet been investigated. We transduced murine bone marrow with retrovirus-expressing FLT3-TKD mutants or FLT3-ITD and transplanted these cells into lethally irradiated mice. Mice that received a transplant of FLT3-ITD developed an oligoclonal myeloproliferative disease as previously described. In contrast, FLT3-TKD mutants induced an oligoclonal lymphoid disorder with longer latency and distinct hematologic manifestations: importantly, induction of the lymphoid phenotype was not due to a low number of transplanted cells. The lymphoid manifestation and longer latency of FLT3-TKD compared with FLT3-ITD mutants together with the lack of influence of FLT3-TKD mutations on the clinical outcome of patients with AML suggest differences in cell signaling between FLT3-TKD mutants and FLT3-ITDs. Indeed strong signal transducers and activators of transcription 5 (STAT5) activation could only be demonstrated for FLT3-ITDs. (Blood. 2005;105:4792-4799)
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