| Literature DB >> 36216899 |
Zuo-Wei Wang1,2, Feng-Ming Zou1,3, Ao-Li Wang1,3, Jing Yang1,3, Rui Jin1,3, Bei-Lei Wang1,3, Li-Juan Shen1,2, Shuang Qi1,3, Juan Liu1,3, Jing Liu4,5, Wen-Chao Wang6,7, Qing-Song Liu8,9,10,11.
Abstract
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.Entities:
Keywords: AZD4547; RIPK1; SIRS model; anti-necroptosis; inhibitors
Year: 2022 PMID: 36216899 DOI: 10.1038/s41401-022-00993-5
Source DB: PubMed Journal: Acta Pharmacol Sin ISSN: 1671-4083 Impact factor: 7.169