E. Piccinin, G. Villani, A. Moschetta
Nature Reviews Gastroenterology & Hepatology, 2018
Alterations of hepatic metabolism are critical to the development of liver disease. The peroxisome proliferator-activated receptor-γ coactivators (PGC1s) are able to orchestrate, on a transcriptional level, different aspects of liver metabolism, such as mitochondrial oxidative phosphorylation, gluconeogenesis and fatty acid synthesis. As modifications affecting both mitochondrial and lipid metabolism contribute to the initiation and/or progression of liver steatosis, nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC), a link between disrupted PGC1 pathways and onset of these pathological conditions has been postulated. However, despite the large quantity of studies, the scenario is still not completely understood, and some issues remain controversial. Here, we discuss the roles of PGC1s in healthy liver and explore their contribution to the pathogenesis and future therapy of NASH and HCC.The liver is a key metabolic organ, and alterations to hepatic metabolism are important for the development of disease. In this Review, the authors explore the central roles of peroxisome proliferator-activated receptor-γ coactivators (PGC1s) in physiological and pathophysiological settings, with a focus on nonalcoholic fatty liver disease and liver cancer.Key pointsPeroxisome proliferator-activated receptor-γ coactivators (PGC1s) have a key role in liver metabolism and contribute to energy homeostasis.PGC1α and PGC1β exert divergent functions on liver metabolism and regulate different pathways.Although the hepatic expression of both PGC1α and PGC1β negatively correlates with nonalcoholic fatty liver disease (NAFLD) severity, hepatocellular carcinoma (HCC) development is inhibited by PGC1α and promoted by PGC1β.Although direct coactivator targeting is problematic, pharmacological modulation of transcriptional and post-transcriptional activators of PGC1s is an appealing therapeutic avenue.
Cited by 59 publications.
Field of study: Medicine