Repurposing crizotinib to target RIPK1-dependent cell death.
Yajie YuMin LiShufang FuXiaoyan HeXinqian HuGuofeng ZhuJia WangXiaoling YouYan MouZhi YeJun WeiYunhong ZhaPublished in: International immunology (2022)
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 FDA-approved compounds and identified a novel use for crizotinib as an inhibitor of RIPK1-dependent cell death. Furthermore, crizotinib rescued TNF-α-induced death in systemic inflammatory response syndrome mice. 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.
Keyphrases
- cell death
- high throughput
- protein kinase
- inflammatory response
- advanced non small cell lung cancer
- oxidative stress
- drug induced
- rheumatoid arthritis
- transcription factor
- metabolic syndrome
- type diabetes
- single cell
- endothelial cells
- diabetic rats
- high glucose
- tyrosine kinase
- lipopolysaccharide induced
- case report
- epidermal growth factor receptor
- toll like receptor
- data analysis
- binding protein
- high fat diet induced
- lps induced