@article{SCI15086,
author = {Yun Chen and Yihang Pan and Yao Guo and Wanke Zhao and Wanting Tina Ho and Jianlong Wang and Mingjiang Xu and Feng-Chun Yang and Zhizhuang Joe Zhao},
title = {Tyrosine kinase inhibitors targeting FLT3 in the treatment of acute myeloid leukemia},
journal = {Stem Cell Investigation},
volume = {4},
number = {6},
year = {2017},
keywords = {},
abstract = {Acute myeloid leukemia (AML) is a cancer of the myeloid lineage of blood cells. Although significant progress has been made in treating many types of cancers during recent years, AML remains a deadly disease with survival rate lagging behind other blood cancers. A combination of toxic chemotherapies has been the standard AML treatment for more than 40 years. With intensive efforts to define the pathogenesis of AML, novel therapeutic drugs targeting key molecular defects in AML are being developed. Mutated in nearly 30% of AML, FMS-like tyrosine kinase 3 (FLT3) represents one of the most attractive targets. FLT3 mutants resulted from either internal tandem duplication (ITD) or point mutations possess enhanced kinase activity and cause constitutive activation of signaling. To date, several small molecule inhibitors of FLT3 have been developed but their clinical efficacy is limited due to a lack of potency and the generation of drug resistance. Therefore, next-generation FLT3 inhibitors overcoming these limitations are urgently in need. This review focuses on the pathological role of mutant FLT3 in the development of AML, the current status of FLT3 inhibitor development, and mechanisms underlining the development of resistance to existing FLT3 inhibitors.},
issn = {2313-0792}, url = {https://sci.amegroups.org/article/view/15086}
}