2005•Chinese Journal of New Drugs and Clinical RemediesRequires access

Progress of treatment with Fms-like receptor tyrosine kinase-3 inhibitors for acute myelogenous leukemia

Xu J

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Abstract

Fms-like receptor tyrosine kinase-3 (FLT3) is a member of the class Ⅲ receptor tyrosine kinase family. Coexpression of wild-type receptor with its ligand,internal tandem duplications (ITD) and activation loop mutations lead to the consistent expression of phosphorylation-activited FLT3. These aberrant expressions of FLT3 have been detected in most acute myelogenous leukemia (AML) providing a prognostic significance. FLT3 inhibitors mainly include 5 varieties and heat shock protein 90(HSP90)inhibitor as well. These agents have shown promising effect on the therapy of AML in experiments and early clinical trials.

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What this paper is about

Fms-like receptor tyrosine kinase-3 (FLT3) is a member of the class Ⅲ receptor tyrosine kinase family. Coexpression of wild-type receptor with its ligand,internal tandem duplications (ITD) and activation loop mutations lead to the consistent expression of phosphorylation-activited FLT3. These aberrant expressions of FLT3 have been detected in most acute myelogenous leukemia (AML) providing a prognostic significance. FLT3 inhibitors mainly include 5 varieties and heat shock protein 90(HSP90)inhibitor as well. These agents have shown promising effect on the therapy of AML in experiments and early clinical trials.

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Available abstract

Fms-like receptor tyrosine kinase-3 (FLT3) is a member of the class Ⅲ receptor tyrosine kinase family. Coexpression of wild-type receptor with its ligand,internal tandem duplications (ITD) and activation loop mutations lead to the consistent expression of phosphorylation-activited FLT3. These aberrant expressions of FLT3 have been detected in most acute myelogenous leukemia (AML) providing a prognostic significance. FLT3 inhibitors mainly include 5 varieties and heat shock protein 90(HSP90)inhibitor as well. These agents have shown promising effect on the therapy of AML in experiments and early clinical trials.

Key concepts: CD135, Receptor tyrosine kinase, ROR1, Tyrosine kinase, Cancer research, AXL receptor tyrosine kinase, Tropomyosin receptor kinase C, Chronic myelogenous leukemia

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