Journal
ACTA PHARMACEUTICA SINICA B
Volume 6, Issue 5, Pages 393-408Publisher
INST MATERIA MEDICA, CHINESE ACAD MEDICAL SCIENCES
DOI: 10.1016/j.apsb.2016.07.003
Keywords
HNF4 alpha; Liver; Drug metabolism; Lipid metabolism; Inflammation; Hormone
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Funding
- NIEHS NIH HHS [R01 ES019487] Funding Source: Medline
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The liver is essential for survival due to its critical role in the regulation of metabolic homeostasis. Metabolism of xenobiotics, such as environmental chemicals and drugs by the liver protects us from toxic effects of these xenobiotics, whereas metabolism of cholesterol, bile acids (BAs), lipids, and glucose provide key building blocks and nutrients to promote the growth or maintain the survival of the organism. As a well-established master regulator of liver development and function, hepatocyte nuclear factor 4 alpha (HNF4 alpha) plays a critical role in regulating a large number of key genes essential for the metabolism of xenobiotics, metabolic wastes, and nutrients. The expression and activity of HNF4 alpha is regulated by diverse hormonal and signaling pathways such as growth hormone, glucocorticoids, thyroid hormone, insulin, transforming growth factor-beta, estrogen, and cytokines. HNF4 alpha appears to play a central role in orchestrating the transduction of extracellular hormonal signaling and intracellular stress/nutritional signaling onto transcriptional changes in the liver. There have been a few reviews on the regulation of drug metabolism, lipid metabolism, cell proliferation, and inflammation by HNF4 alpha. However, the knowledge on how the expression and transcriptional activity of HNF4 alpha is modulated remains scattered. Herein I provide comprehensive review on the regulation of expression and transcriptional activity of HNF4 alpha, and how HNF4 alpha crosstalks with diverse extracellular and intracellular signaling pathways to regulate genes essential in liver pathophysiology. (C) 2016 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
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