Receptor proximal kinases in NF-κB signaling as potential therapeutic targets in cancer and inflammation

被引:53
|
作者
Verstrepen, Lynn [1 ,2 ]
Beyaert, Rudi [1 ,2 ]
机构
[1] VIB, Inflammat Res Ctr, Unit Mol Signal Transduct Inflammat, Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9000 Ghent, Belgium
关键词
Therapy; Kinase; NF-kappa B; Inflammation; Cancer; RHO-ASSOCIATED KINASE; INTERLEUKIN-1; RECEPTOR; IKK-BETA; C-THETA; DIFFERENTIAL REGULATION; PREVENTS INFLAMMATION; BACTERIAL-INFECTIONS; ACTIVATION PATHWAYS; CRYSTAL-STRUCTURE; DEPENDENT KINASE;
D O I
10.1016/j.bcp.2014.10.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many signaling pathways leading to activation of transcription factors and gene expression are characterized by phosphorylation events mediated by specific kinases. The transcription factor NF-kappa B plays a key role in multiple cellular processes, including immune signaling, inflammation, development, proliferation and survival. Dysregulated NF-kappa B activation is associated with autoimmunity, chronic inflammation and cancer. Activation of NF-kappa B requires I kappa B kinase (IKK)alpha or beta, the activity of which is regulated via phosphorylation by specific IRK kinases and by autophosphorylation. Receptor specificity is further obtained by the use of multiple upstream receptor proximal kinases. We review the identities of several IKK regulatory kinases as well as the proposed molecular mechanisms. In addition, we discuss the potential for therapeutic targeting of some of these kinases in the context of inflammatory diseases and cancer. (C) 2014 Elsevier Inc. All rights reserved.
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页码:519 / 529
页数:11
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