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Department of Medicine and Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, New York 10461
Toxin-induced liver injury was formerly
considered a passive biochemical event, but recent evidence has
demonstrated that signal transduction pathways actively modulate the
hepatocyte's response to this form of injury. Investigations have
examined the effects of a variety of toxins on the activation of
receptor-coupled signal transduction, mitogen-activated protein
kinases, and Fas signaling, as well as the generation of second
messengers such as ceramide and nitric oxide. Many of these pathways
culminate in the activation of transcription factors such as activator
protein-1, c-Myc, or nuclear factor-
B. This Themes
article discusses the effects of toxic injury on these signaling
pathways and their known functions in regulating hepatocyte death and
proliferation following injury.
mitogen-activated protein kinase; ceramide; nitric oxide; activator
protein-1; c-Myc; nuclear factor-
B; Fas
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