Design, Synthesis, and Biological Activities Evaluation of Type I FLT3 Inhibitors for the Treatment of Acute Myeloid Leukemia

The abnormal overexpression of FLT3 kinase is intimately associated with pathogenesis of acute myeloid leukemia (AML), positioning FLT3 inhibitors as pivotal therapeutic agents. Despite the availability of three FDA-approved FLT3 inhibitors, their clinical utility is hampered by resistance stemming from tyrosine kinase domain (TKD) mutations. Through an integrative analysis of case studies, we identified a potential advantage of type I FLT3 inhibitors in overcoming TKD mutation-induced resistance. Structure-activity relationships (SAR) analysis indicated that FW-1 exhibited over 50% inhibition against FLT3 at a concentration of 1 μM and demonstrated potent activity against AML cell lines MV4-11 (IC<sub>50</sub> = 2.68 μM) and MOLM-13 (IC<sub>50</sub> = 1.03 μM). In our cellular mechanistic studies, FW-1 also effectively induced apoptosis by arresting cell cycle progression in the G0/G1 phase. This study introduces FW-1 as a promising lead for type I FLT3 inhibitor, warranting further optimization.

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Publication Details

Journal
Drug Development Research
Published
2024-11-21
DOI
https://doi.org/10.1002/ddr.70022
Citations
1
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
0.45

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article

Design, Synthesis, and Biological Activities Evaluation of Type I FLT3 Inhibitors for the Treatment of Acute Myeloid Leukemia

Q. L. Niu, Nian‐Guang Li, Shan‐Liang Sun, Meng‐Yuan Zhang et al.
1 citations
Drug Development Research
Acute Myeloid Leukemia Research
0.45
article

Design, Synthesis, and Biological Activities Evaluation of Type I FLT3 Inhibitors for the Treatment of Acute Myeloid Leukemia

Q. L. Niu, Nian‐Guang Li, Shan‐Liang Sun, Meng‐Yuan Zhang, Wei‐Chen Dai, Xin Jing, Shijie Zhou, Yan‐Cheng Yu, Jin Yang, Zhi‐Hao Shi, Zixuan Wang, Qingqing Li, Xiaolong Wang, Jingjing Wang, Yan Zhang, Yun Zhou, Xin Xue, Ning Ding, Yujing Xu, Qing‐Xin Wang, Xi Liang, Tian‐Hua Wei, Yue‐Chu Li
article en
1 citations

Abstract

The abnormal overexpression of FLT3 kinase is intimately associated with pathogenesis of acute myeloid leukemia (AML), positioning FLT3 inhibitors as pivotal therapeutic agents. Despite the availability of three FDA-approved FLT3 inhibitors, their clinical utility is hampered by resistance stemming from tyrosine kinase domain (TKD) mutations. Through an integrative analysis of case studies, we identified a potential advantage of type I FLT3 inhibitors in overcoming TKD mutation-induced resistance. Structure-activity relationships (SAR) analysis indicated that FW-1 exhibited over 50% inhibition against FLT3 at a concentration of 1 μM and demonstrated potent activity against AML cell lines MV4-11 (IC<sub>50</sub> = 2.68 μM) and MOLM-13 (IC<sub>50</sub> = 1.03 μM). In our cellular mechanistic studies, FW-1 also effectively induced apoptosis by arresting cell cycle progression in the G0/G1 phase. This study introduces FW-1 as a promising lead for type I FLT3 inhibitor, warranting further optimization.

Drug Development ResearchVol. 85(8)
Nanjing University of Chinese Medicine (CN), China Pharmaceutical University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 31%
Acute Myeloid Leukemia Research
0.45
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