| Literature DB >> 27871061 |
Xiaomeng Ren1, Xinzhi Li1, Linna Jia1, Deheng Chen2, Hai Hou3, Liangyou Rui4, Yujun Zhao5, Zheng Chen6.
Abstract
Potent and selective chemical probes are valuable tools for discovery of novel treatments for human diseases. NF-κB-inducing kinase (NIK) is a key trigger in the development of liver injury and fibrosis. Whether inhibition of NIK activity by chemical probes ameliorates liver inflammation and injury is largely unknown. In this study, a small-molecule inhibitor of NIK, B022, was found to be a potent and selective chemical probe for liver inflammation and injury. B022 inhibited the NIK signaling pathway, including NIK-induced p100-to-p52 processing and inflammatory gene expression, both in vitro and in vivo Furthermore, in vivo administration of B022 protected against not only NIK but also CCl4-induced liver inflammation and injury. Our data suggest that inhibition of NIK is a novel strategy for treatment of liver inflammation, oxidative stress, and injury.-Ren, X., Li, X., Jia, L., Chen, D., Hou, H., Rui, L., Zhao, Y., Chen, Z. A small-molecule inhibitor of NF-κB-inducing kinase (NIK) protects liver from toxin-induced inflammation, oxidative stress, and injury. © FASEB.Entities:
Keywords: CCl4; NIK; inflammation; liver injury
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Year: 2016 PMID: 27871061 DOI: 10.1096/fj.201600840R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191