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Necroptosis is a form of regulated necrotic cell death mediated by receptor-interacting serine/threonine-protein kinase 1 (RIPK1) and RIPK3. Necroptotic cell death contributes to the pathophysiology of several disorders involving tissue damage, including myocardial infarction, stroke and ischemia-reperfusion injury. However, no inhibitors of necroptosis are currently in clinical use. Here we performed a phenotypic screen for small-molecule inhibitors of tumor necrosis factor-alpha (TNF-α)-induced necroptosis in Fas-associated protein with death domain (FADD)-deficient Jurkat cells using a representative panel of Food and Drug Administration (FDA)-approved drugs. We identified two anti-cancer agents, ponatinib and pazopanib, as submicromolar inhibitors of necroptosis. Both compounds inhibited necroptotic cell death induced by various cell death receptor ligands in human cells, while not protecting from apoptosis. Ponatinib and pazopanib abrogated phosphorylation of mixed lineage kinase domain-like protein (MLKL) upon TNF-α-induced necroptosis, indicating that both agents target a component upstream of MLKL. An unbiased chemical proteomic approach determined the cellular target spectrum of ponatinib, revealing key members of the necroptosis signaling pathway. We validated RIPK1, RIPK3 and transforming growth factor-β-activated kinase 1 (TAK1) as novel, direct targets of ponatinib by using competitive binding, cellular thermal shift and recombinant kinase assays. Ponatinib inhibited both RIPK1 and RIPK3, while pazopanib preferentially targeted RIPK1. The identification of the FDA-approved drugs ponatinib and pazopanib as cellular inhibitors of necroptosis highlights them as potentially interesting for the treatment of pathologies caused or aggravated by necroptotic cell death.

Original publication

DOI

10.1038/cddis.2015.130

Type

Journal article

Journal

Cell Death Dis

Publication Date

21/05/2015

Volume

6

Keywords

3T3 Cells, Animals, Apoptosis, Cell Line, Tumor, Fas-Associated Death Domain Protein, HEK293 Cells, HT29 Cells, Humans, Imidazoles, Jurkat Cells, L Cells (Cell Line), MAP Kinase Kinase Kinases, Mice, Necrosis, Phosphorylation, Protein Binding, Protein Kinase Inhibitors, Protein Kinases, Pyridazines, Pyrimidines, Receptor-Interacting Protein Serine-Threonine Kinases, Sulfonamides, Tumor Necrosis Factor-alpha