FLT3 Mutations in Acute Myeloid Leukemia: Key Concepts and Emerging Controversies

VE Kennedy, CC Smith - Frontiers in Oncology, 2020 - frontiersin.org
The FLT3 receptor is overexpressed on the majority of acute myeloid leukemia (AML) blasts.
Mutations in FLT3 are the most common genetic alteration in AML, identified in …

FLT3 inhibitors in acute myeloid leukemia: current status and future directions

M Larrosa-Garcia, MR Baer - Molecular cancer therapeutics, 2017 - AACR
The receptor tyrosine kinase fms-like tyrosine kinase 3 (FLT3), involved in regulating
survival, proliferation, and differentiation of hematopoietic stem/progenitor cells, is …

[HTML][HTML] Molecular targeted therapy of cancer: The progress and future prospect

X Ke, L Shen - Frontiers in Laboratory Medicine, 2017 - Elsevier
Cancer has become a major public health problem worldwide. Researches focus on the
new approaches for cancer treatments that involve the specific targets of the cancer disease …

B cells in atherosclerosis: mechanisms and potential clinical applications

T Pattarabanjird, C Li, C McNamara - Basic to Translational Science, 2021 - jacc.org
Because atherosclerotic cardiovascular disease is a leading cause of death worldwide,
understanding inflammatory processes underpinning its pathology is critical. B cells have …

Small-molecule fms-like tyrosine kinase 3 inhibitors: an attractive and efficient method for the treatment of acute myeloid leukemia

Y Zhong, RZ Qiu, SL Sun, C Zhao, TY Fan… - Journal of medicinal …, 2020 - ACS Publications
Fms-like tyrosine kinase 3 (FLT3) is an important member of the class III receptor tyrosine
kinase (RTK) family, which is involved in the proliferation of hematopoietic cells and …

[HTML][HTML] Therapeutic targeting of FLT3 in acute myeloid leukemia: current status and novel approaches

M Tecik, A Adan - OncoTargets and Therapy, 2022 - ncbi.nlm.nih.gov
FMS-like tyrosine kinase 3 (FLT3) is mutated in approximately 30% of acute myeloid
leukemia (AML) patients. The presence of FLT3-ITD (internal tandem duplication, 20–25%) …

Synergistic targeting of DNA-PK and KIT signaling pathways in KIT mutant acute myeloid leukemia

HC Murray, K Miller, JS Brzozowski, RGS Kahl… - Molecular & Cellular …, 2023 - ASBMB
Acute myeloid leukemia (AML) is the most common and aggressive form of acute leukemia,
with a 5-year survival rate of just 24%. Over a third of all AML patients harbor activating …

Targeting tyrosine kinases in acute myeloid leukemia: why, who and how?

S Fernandez, V Desplat, A Villacreces… - International journal of …, 2019 - mdpi.com
Acute myeloid leukemia (AML) is a myeloid malignancy carrying a heterogeneous molecular
panel of mutations participating in the blockade of differentiation and the increased …

Pyrimidine-fused dinitrogenous penta-heterocycles as a privileged scaffold for anti-cancer drug discovery

W Li, J Zhang, M Wang, R Dong, X Zhou… - Current Topics in …, 2022 - ingentaconnect.com
Pyrimidine-fused derivatives that are the inextricable part of DNA and RNA play a key role in
the normal life cycle of cells. Pyrimidine-fused dinitrogenous penta-heterocycles, including …

Discovery of 1-(4-(4-Amino-3-(4-(2-morpholinoethoxy)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)phenyl)-3-(5-(tert-butyl)isoxazol-3-yl)urea (CHMFL-FLT3-213) as a …

A Wang, X Li, C Chen, H Wu, Z Qi, C Hu… - Journal of Medicinal …, 2017 - ACS Publications
FLT3-ITD mutant has been observed in about 30% of AML patients and extensively studied
as a drug discovery target. On the basis of our previous study that ibrutinib (9) exhibited …