PTEN in Non-Alcoholic Fatty Liver Disease/Non-Alcoholic Steatohepatitis and Cancer

被引:46
作者
Peyrou, Marion [1 ]
Bourgoin, Lucie [1 ]
Foti, Michelangelo [1 ]
机构
[1] CMU, Dept Cellular Physiol & Metab, Geneva Med Fac, CH-1211 Geneva 4, Switzerland
关键词
PTEN; Obesity; Liver; Insulin resistance; Steatosis; Fibrosis; Hepatocellular carcinoma; TUMOR-SUPPRESSOR PTEN; HEPATOCELLULAR-CARCINOMA; TENSIN HOMOLOG; INSULIN-RESISTANCE; DOWN-REGULATION; CELL-MIGRATION; UP-REGULATION; PROTEIN STABILITY; PPAR-GAMMA; POSTTRANSLATIONAL REGULATION;
D O I
10.1159/000282095
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The tumor suppressor PTEN is a protein/phosphoinositide phosphatase regulating the PI3K/Akt signaling pathway and is mutated or deleted in a variety of human cancers, including hepatocellular carcinoma (HCC). Accumulating evidence indicates that alterations of PTEN expression and activity in hepatocytes are common and recurrent molecular events associated with liver disorders of various etiologies including obesity, the metabolic syndrome, hepatitis B virus/hepatitis C virus infection and abusive alcohol consumption. Genetic and molecular studies, particularly in the context of non-alcoholic fatty liver disease (NAFLD), support a critical role for PTEN in hepatic insulin sensitivity and the development of steatosis, steatohepatitis and fibrosis. PTEN mutations/deletion or low PTEN expression are also associated with diverse liver malignancies, suggesting a critical role for PTEN in hepatic cancers. This review provides an overview of the current knowledge on pathological dysregulations of PTEN expression/activity in the liver with obesity and the metabolic syndrome, and the role of this enzyme in the development of non-alcoholic fatty liver disease and hepatocellular carcinoma. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:236 / 246
页数:11
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