TAK1 regulates hepatic cell survival and carcinogenesis

被引:119
作者
Roh, Yoon Seok [1 ]
Song, Jingyi [1 ]
Seki, Ekihiro [1 ]
机构
[1] Univ Calif San Diego, Dept Med, Sch Med, La Jolla, CA 92093 USA
关键词
HCC; NF-kappa B; TGF-beta; Liver cancer; Apoptosis; NF-KAPPA-B; ACTIVATED KINASE 1; BETA SIGNAL-TRANSDUCTION; TGF-BETA; IN-VIVO; POLYUBIQUITIN CHAINS; DEUBIQUITINASE CYLD; MEDIATED ACTIVATION; INDUCED APOPTOSIS; GENOTOXIC STRESS;
D O I
10.1007/s00535-013-0931-x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
TGF-beta-activated kinase 1 (TAK1 or MAP3K7) is an intracellular hub molecule that regulates both nuclear factor-kappa B (NF-kappa B) and mitogen-activated protein kinase (MAPK) signaling pathways that play key roles in development, cell survival, immune response, metabolism, and carcinogenesis. TAK1 activity is tightly regulated by its binding proteins, TAB1 and TAB2/TAB3, as well as by post-translational modification including ubiquitination and phosphorylation. Accumulating evidence demonstrates that TAK1 plays a role in tumor initiation, progression, and metastasis as a tumor prompter or tumor suppressor. An understanding of the role of TAK1 in liver physiology and diseases is required for the development of therapeutic agencies targeting TAK1. In this review, we highlight the activation mechanism and pathophysiological roles of TAK1 in the liver.
引用
收藏
页码:185 / 194
页数:10
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