Nonalcoholic fatty liver disease (NAFLD) is the most common form of liver pathologies and is associated with obesity and the metabolic syndrome, which represents a range of fatty liver diseases associated with an increased risk of type 2 diabetes. Molecular mechanisms underlying how to make transition from simple fatty liver to nonalcoholic steatohepatitis (NASH) are not well understood. However, accumulating evidence indicates that deregulation of the phosphatidylinositol 3-kinase (PI3K)/AKT pathway in hepatocytes is a common molecular event associated with metabolic dysfunctions including obesity, metabolic syndrome, and the NAFLD. A tumor suppressor PTEN negatively regulates the PI3K/AKT pathways through its lipid phosphatase activity. Molecular studies in the NAFLD support a key role for PTEN in hepatic insulin sensitivity and the development of steatosis, steatohepatitis, and fibrosis. We review recent studies on the features of the PTEN and the PI3K/AKT pathway and discuss the protein functions in the signaling pathways involved in the NAFLD. The molecular mechanisms contributing to the diseases are the subject of considerable investigation, as a better understanding of the pathogenesis will lead to novel therapies for a condition.
Keyphrases
- pi k akt
- metabolic syndrome
- signaling pathway
- insulin resistance
- cell proliferation
- cell cycle arrest
- high fat diet induced
- uric acid
- liver fibrosis
- weight loss
- high fat diet
- protein kinase
- type diabetes
- fatty acid
- skeletal muscle
- cell therapy
- cardiovascular risk factors
- single molecule
- adipose tissue
- single cell
- epithelial mesenchymal transition
- induced apoptosis
- physical activity
- mesenchymal stem cells
- stem cells
- body mass index
- protein protein
- small molecule
- oxidative stress