The Physiological and Pathophysiological Role of IL-6/STAT3-Mediated Signal Transduction and STAT3 Binding Partners in Therapeutic Applications

被引:0
|
作者
Matsuda, Tadashi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Immunol, Kita 12,Nishi 6,Kita Ku, Sapporo 0600812, Japan
基金
日本学术振兴会;
关键词
interleukin 6 (IL-6); signal transducer and activator of transcription 3 (STAT3); signal transduction; inflammation; immune disease; therapy; NF-KAPPA-B; NONRECEPTOR TYROSINE KINASE; SMALL-MOLECULE INHIBITOR; STIMULATORY FACTOR-II; ZINC-FINGER PROTEINS; FUNCTIONAL INTERACTIONS; MESSENGER-RNA; TRANSCRIPTIONAL ACTIVATION; SERINE PHOSPHORYLATION; INTERLEUKIN-6; RECEPTOR;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The interleukin 6 (IL-6) family of cytokines is defined by the usage of gp130, a common beta-receptor signaling subunit, which promotes a variety of signals. They induce many biological functions on many cell types, including immune and inflammatory cells. They also exhibit hormone-like features, which are involved in homeostatic processes. Signal transducer and activator of transcription 3 (STAT3) is a significant signaling molecule fundamental in regulating IL-6/gp130 and is highly implicated in pathological conditions; therefore, STAT3 activation is tightly regulated through various mechanisms and at multiple levels. There is a large amount of information about STAT3-interacting proteins, which positively or negatively regulate STAT3 activity. This review is focused on IL-6-mediated signal transduction and the introduction of novel STAT3-binding partners. The review will help develop new strategies for clinically controlling the functions of IL-6/STAT3.
引用
收藏
页码:364 / 378
页数:15
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