Discovery of Janus Kinase 2 (JAK2) and Histone Deacetylase (HDAC) Dual Inhibitors as a Novel Strategy for the Combinational Treatment of Leukemia and Invasive Fungal Infections

被引:93
|
作者
Huang, Yahui [1 ]
Dong, Guoqiang [1 ]
Li, Huanqiu [2 ]
Liu, Na [1 ]
Zhang, Wannian [1 ]
Sheng, Chunquan [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, 325 Guohe Rd, Shanghai 200433, Peoples R China
[2] Soochow Univ, Coll Pharmaceut Sci, Suzhou 215123, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
RESISTANCE; DESIGN; SENSITIVITY; CANCER; RUXOLITINIB; EPIGENETICS; MACROCYCLE; THERAPY;
D O I
10.1021/acs.jmedchem.8b00393
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Clinically, leukemia patients often suffer from the limited efficacy of chemotherapy and high risks of infection by invasive fungal pathogens Herein, a novel therapeutic strategy was developed in which a small molecule can simultaneously treat leukemia and invasive fungal infections (IFIs).Novel Janus kinase 2 (JAK2) and histone deacetylase (HDAC) dual inhibitors were identified to possess potent anti-proliferative activity toward hematological cell lines and excellent synergistic effects with fluconazole to treat resistant Candida albicans infections.In particular, compound 20a, a highly active and selective JAK2/ HDAC6 dual inhibitor, showed excellent in vivo antitumor efficacy in several acute myeloid leukemia (AML) models and synergized with fluconazole for the treatment of resistant C. albicans infections. This study highlights the therapeutic potential of JAK2/HDAC dual inhibitors in treating AML and IFIs and provides an efficient strategy for multitargeting drug discovery.
引用
收藏
页码:6056 / 6074
页数:19
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