重新利用克唑替尼靶向ripk1依赖性细胞死亡。

IF 4.8 4区 医学 Q2 IMMUNOLOGY International immunology Pub Date : 2023-05-08 DOI:10.1093/intimm/dxac061
Yajie Yu, Min Li, Shufang Fu, Xiaoyan He, Xinqian Hu, Guofeng Zhu, Jia Wang, Xiaoling You, Yan Mou, Zhi Ye, Jun Wei, Yunhong Zha
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引用次数: 0

摘要

受体相互作用蛋白激酶1 (Receptor-interacting protein kinase 1, RIPK1)已成为细胞死亡和炎症的关键调节因子,与许多炎症和退行性疾病的发病机制有关。因此,RIPK1被认为是许多这些疾病的治疗靶点。然而,目前临床上还没有ripk1介导的细胞死亡的药物抑制剂。认识到重新用途的药物具有加速的临床开发管道,在这里,我们对食品和药物管理局(FDA)批准的化合物进行了高通量药物筛选,并确定了克唑替尼作为ripk1依赖性细胞死亡抑制剂的新用途。此外,克唑替尼可挽救TNF-α-诱导的全身炎症反应综合征小鼠的死亡。克里唑替尼直接抑制RIPK1激酶活性。这些发现确定了一种已建立的化合物的新用途,并有望加速ripk1谱系疾病的药物开发。
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Repurposing crizotinib to target RIPK1-dependent cell death.

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-α-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.

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来源期刊
International immunology
International immunology 医学-免疫学
CiteScore
9.30
自引率
2.30%
发文量
51
审稿时长
6-12 weeks
期刊介绍: International Immunology is an online only (from Jan 2018) journal that publishes basic research and clinical studies from all areas of immunology and includes research conducted in laboratories throughout the world.
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