4.7 Review

TAK1 regulates hepatic cell survival and carcinogenesis

Journal

JOURNAL OF GASTROENTEROLOGY
Volume 49, Issue 2, Pages 185-194

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s00535-013-0931-x

Keywords

HCC; NF-kappa B; TGF-beta; Liver cancer; Apoptosis

Funding

  1. NIH [R01AA02172, R01DK085252, P42 ES010337]
  2. UCSD Digestive Diseases Research Development Center [DK080506]

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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.

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