Systems biology approaches for studying the pathogenesis of non-alcoholic fatty liver disease

被引:15
作者
Fisher, Ciaran P. [1 ]
Kierzek, Andrzej M. [1 ]
Plant, Nick J. [1 ]
Moore, J. Bernadette [1 ]
机构
[1] Univ Surrey, Fac Hlth & Med Sci, Guildford GU2 7XH, Surrey, England
基金
英国生物技术与生命科学研究理事会;
关键词
Non-alcoholic fatty liver disease; Network; Metabolism; Systems biology; Modelling; Regulation; Simulation; METABOLIC NETWORK RECONSTRUCTION; IN-VITRO SYSTEMS; HUMAN GENOME; GLOBAL RECONSTRUCTION; SIGNALING NETWORKS; MOUSE HEPATOCYTES; ESCHERICHIA-COLI; GENE-EXPRESSION; CELL-LINES; MODELS;
D O I
10.3748/wjg.v20.i41.15070
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Non-alcoholic fatty liver disease (NAFLD) is a progressive disease of increasing public health concern. In western populations the disease has an estimated prevalence of 20%-40%, rising to 70%-90% in obese and type. diabetic individuals. Simplistically, NAFLD is the macroscopic accumulation of lipid in the liver, and is viewed as the hepatic manifestation of the metabolic syndrome. However, the molecular mechanisms mediating both the initial development of steatosis and its progression through non-alcoholic steatohepatitis to debilitating and potentially fatal fibrosis and cirrhosis are only partially understood. Despite increased research in this field, the development of non-invasive clinical diagnostic tools and the discovery of novel therapeutic targets has been frustratingly slow. We note that, to date, NAFLD research has been dominated by in vivo experiments in animal models and human clinical studies. Systems biology tools and novel computational simulation techniques allow the study of large-scale metabolic networks and the impact of their dysregulation on health. Here we review current systems biology tools and discuss the benefits to their application to the study of NAFLD. We propose that a systems approach utilising novel in silico modelling and simulation techniques is key to a more comprehensive, better targeted NAFLD research strategy. Such an approach will accelerate the progress of research and vital translation into clinic. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:15070 / 15078
页数:9
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