Roles for PI3K/AKT/PTEN Pathway in Cell Signaling of Nonalcoholic Fatty Liver Disease.

ISRN endocrinology Pub Date : 2013-01-01 Epub Date: 2013-01-30 DOI:10.1155/2013/472432
Satoru Matsuda, Mayumi Kobayashi, Yasuko Kitagishi
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引用次数: 125

Abstract

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.

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PI3K/AKT/PTEN通路在非酒精性脂肪肝细胞信号传导中的作用
非酒精性脂肪性肝病(NAFLD)是最常见的肝脏病理形式,与肥胖和代谢综合征有关,代谢综合征是一系列与2型糖尿病风险增加相关的脂肪性肝病。如何从单纯性脂肪肝转变为非酒精性脂肪性肝炎(NASH)的分子机制尚不清楚。然而,越来越多的证据表明,肝细胞中磷脂酰肌醇3-激酶(PI3K)/AKT通路的失调是与代谢功能障碍(包括肥胖、代谢综合征和NAFLD)相关的常见分子事件。肿瘤抑制因子PTEN通过其脂质磷酸酶活性负调控PI3K/AKT通路。NAFLD的分子研究支持PTEN在肝脏胰岛素敏感性和脂肪变性、脂肪性肝炎和纤维化的发展中的关键作用。我们回顾了PTEN和PI3K/AKT通路的最新研究,并讨论了NAFLD信号通路中涉及的蛋白质功能。导致这些疾病的分子机制是大量研究的主题,因为更好地了解其发病机制将导致新的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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