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靶向 RIPK1/RIPK3 的抑制剂:旧药与新药。

Inhibitors Targeting RIPK1/RIPK3: Old and New Drugs.

机构信息

VIB Center for Inflammation Research, Ghent 9052, Belgium; Department of Biomedical Molecular Biology (DBMB), Ghent University, Ghent 9052, Belgium.

Laboratory of Medicinal Chemistry, University of Antwerp, Antwerp B-2610, Belgium.

出版信息

Trends Pharmacol Sci. 2020 Mar;41(3):209-224. doi: 10.1016/j.tips.2020.01.002. Epub 2020 Feb 5.

Abstract

The scaffolding function of receptor-interacting protein kinase 1 (RIPK1) regulates prosurvival signaling and inflammatory gene expression, while its kinase activity mediates both apoptosis and necroptosis; the latter involving RIPK3 kinase activity. The mutual transition between the scaffold and kinase functions of RIPK1 is regulated by (de)ubiquitylation and (de)phosphorylation. RIPK1-mediated cell death leads to disruption of epithelial barriers and/or release of damage-associated molecular patterns (DAMPs), cytokines, and chemokines, propagating inflammatory and degenerative diseases. Many drug development programs have pursued targeting RIPK1, and to a lesser extent RIPK3 kinase activity. In this review, we classify existing and novel small-molecule drugs based on their pharmacodynamic (PD) type I, II, and III binding mode. Finally, we discuss their applicability and therapeutic potential in inflammatory and degenerative experimental disease models.

摘要

受体相互作用蛋白激酶 1(RIPK1)的支架功能调节存活信号和炎症基因表达,而其激酶活性介导凋亡和坏死性凋亡;后者涉及 RIPK3 激酶活性。RIPK1 的支架和激酶功能的相互转换受(去)泛素化和(去)磷酸化调节。RIPK1 介导的细胞死亡导致上皮屏障的破坏和/或损伤相关分子模式(DAMPs)、细胞因子和趋化因子的释放,从而引发炎症和退行性疾病。许多药物开发计划都在追求靶向 RIPK1,在较小程度上也靶向 RIPK3 激酶活性。在这篇综述中,我们根据药效学(PD)的 I 型、II 型和 III 型结合模式对现有的和新型小分子药物进行分类。最后,我们讨论了它们在炎症和退行性实验疾病模型中的适用性和治疗潜力。

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