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Am J Physiol Gastrointest Liver Physiol 290: G583-G589, 2006; doi:10.1152/ajpgi.00422.2005
0193-1857/06 $8.00
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THEMES

Mechanisms of Liver Injury. I. TNF-{alpha}-induced liver injury: role of IKK, JNK, and ROS pathways

Robert F. Schwabe and David A. Brenner

Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York

TNF-{alpha} activates several intracellular pathways to regulate inflammation, cell death, and proliferation. In the liver, TNF-{alpha} is not only a mediator of hepatotoxicity but also contributes to the restoration of functional liver mass by driving hepatocyte proliferation and liver regeneration. This review summarizes recent advances in TNF-{alpha} signaling mechanisms that demonstrate how the IKK, ROS, and JNK pathways interact with each other to regulate hepatocyte apoptosis and proliferation. Activation of these pathways is causatively linked to liver injury induced by concanavalin A, TNF-{alpha}, and ischemia-reperfusion and to liver regeneration and hepatocarcinogenesis. In light of recent findings, pharmacological inhibitors of JNK and IKK and antioxidants may be promising new tools for the treatment of hepatitis, ischemia-reperfusion injury, and hepatocellular carcinoma.

hepatocyte; reactive oxygen species; c-Jun NH2-terminal kinase; I{kappa}B kinase



Address for reprint requests and other correspondence: Correspondence to: R. F. Schwabe, Dept. of Medicine, Columbia Univ. College of Physicians and Surgeons, P&S 9-460, 630W 168th St., New York, NY 10032 (e-mail: rfs2102{at}columbia.edu)




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