Repurposing crizotinib to target RIPK1-dependent cell death

被引:2
作者
Yu, Yajie [1 ]
Li, Min [1 ]
Fu, Shufang [2 ]
He, Xiaoyan [1 ]
Hu, Xinqian [1 ]
Zhu, Guofeng [1 ]
Wang, Jia [1 ]
You, Xiaoling [1 ]
Mou, Yan [1 ]
Ye, Zhi [1 ]
Wei, Jun [1 ]
Zha, Yunhong [1 ]
机构
[1] Three Gorges Univ, Hosp Yichang 1, Inst Neural Regenerat & Repair, Dept Neurol,Coll Med, Yichang 443000, Peoples R China
[2] Three Gorges Univ, Hosp Yichang 1, Dept Pediat, Coll Med, Yichang 443000, Peoples R China
关键词
inflammation; SIRS; INFLAMMATORY RESPONSE; ADP-GLO; RIPK1; NECROPTOSIS; ACTIVATION; ASSAY;
D O I
10.1093/intimm/dxac061
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Receptor-interacting protein kinase 1 (RIPK1) has emerged as a key regulator of cell death and inflammation, which are implicated in the pathogenesis of many inflammatory and degenerative diseases. RIPK1 is therefore a putative therapeutic target in many of these diseases. However, no pharmacological inhibitor of RIPK1-mediated cell death is currently in clinical use. Recognizing that a repurposed drug has an expedited clinical development pipeline, here we performed a high-throughput drug screen of Food and Drug Administration (FDA)-approved compounds and identified a novel use for crizotinib as an inhibitor of RIPK1-dependent cell death. Furthermore, crizotinib rescued TNF-alpha-induced death in mice with systemic inflammatory response syndrome. RIPK1 kinase activity was directly inhibited by crizotinib. These findings identify a new use for an established compound and are expected to accelerate drug development for RIPK1-spectrum disorders.
引用
收藏
页码:221 / 230
页数:10
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