坏死性下垂
裂谷1
药物重新定位
激酶
重新调整用途
癌症研究
程序性细胞死亡
细胞生物学
药理学
细胞凋亡
生物
药品
生物化学
生态学
作者
Zuowei Wang,Fengming Zou,Aoli Wang,Jing Yang,Rui Jin,Beilei Wang,Lijuan Shen,Shuang Qi,Juan Liu,Jing Liu,Wenchao Wang,Qingsong Liu
标识
DOI:10.1038/s41401-022-00993-5
摘要
Necroptosis is a form of regulated necrosis involved in various pathological diseases. The process of necroptosis is controlled by receptor-interacting kinase 1 (RIPK1), RIPK3, and pseudokinase mixed lineage kinase domain-like protein (MLKL), and pharmacological inhibition of these kinases has been shown to have therapeutic potentials in a variety of diseases. In this study, using drug repurposing strategy combined with high-throughput screening (HTS), we discovered that AZD4547, a previously reported FGFR inhibitor, is able to interfere with necroptosis through direct targeting of RIPK1 kinase. In both human and mouse cell models, AZD4547 blocked RIPK1-dependent necroptosis. In addition, AZD4547 rescued animals from TNF-induced lethal shock and inflammatory responses. Together, our study demonstrates that AZD4547 is a potent and selective inhibitor of RIPK1 with therapeutic potential for the treatment of inflammatory disorders that involve necroptosis.
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