| Literature DB >> 32247850 |
Xia Qin1, Longmiao Hu1, Shen-Nan Shi2, Xiaofei Chen3, Chunlin Zhuang3, Wen Zhang4, Siriporn Jitkaew5, Xiufeng Pang6, Jianqiang Yu7, Ye-Xiong Tan8, Hong-Yang Wang9, Zhenyu Cai10.
Abstract
Necroptosis is a form of programmed, caspase-independent cell death that is involved in various pathologic disorders such as ischemia/reperfusion injury, acute kidney injury and inflammatory bowel diseases. Identification of necroptosis inhibitors has great therapeutic potential for the treatment of necroptosis-associated diseases. In this study, we identified that the Bcr-Abl inhibitor GNF-7 was a potent inhibitor of necroptosis. GNF-7 inhibited necroptosis in both human and mouse cells, while not protecting cells from apoptosis. Drug affinity responsive target stability assay (DARTS) demonstrated that it binded with RIPK1 and RIPK3. GNF-7 inhibited RIPK1 and RIPK3 kinase activities and thus disrupted RIPK1-RIPK3 necrosome complex formation. In vivo, GNF-7 ameliorated both cisplatin- and ischemia/reperfusion-induced AKI. Orally administration of GNF-7 attenuated renal cell necrosis and reduced pro-inflammatory responses in mouse models of AKI. Taken together, our study shows that GNF-7 is a novel necroptosis inhibitor and has great potential for the treatment of acute renal inflammatory disorders by targeting both RIPK1 and RIPK3 kinases.Entities:
Keywords: Acute kidney injury; GNF-7; Necroptosis; RIPK1; RIPK3
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Year: 2020 PMID: 32247850 DOI: 10.1016/j.bcp.2020.113947
Source DB: PubMed Journal: Biochem Pharmacol ISSN: 0006-2952 Impact factor: 5.858