系统生物学
生物网络
计算生物学
串扰
疾病
脂肪肝
医学
肝硬化
药物发现
肝细胞癌
生物途径
肝病学
肝病
生物
生物信息学
癌症研究
病理
内科学
基因表达
物理
生物化学
光学
基因
作者
Adil Mardinoğlu,Jan Borén,Ulf Smith,Mathias Uhlén,Jens Nielsen
标识
DOI:10.1038/s41575-018-0007-8
摘要
Detailed insights into the biological functions of the liver and an understanding of its crosstalk with other human tissues and the gut microbiota can be used to develop novel strategies for the prevention and treatment of liver-associated diseases, including fatty liver disease, cirrhosis, hepatocellular carcinoma and type 2 diabetes mellitus. Biological network models, including metabolic, transcriptional regulatory, protein-protein interaction, signalling and co-expression networks, can provide a scaffold for studying the biological pathways operating in the liver in connection with disease development in a systematic manner. Here, we review studies in which biological network models were used to integrate multiomics data to advance our understanding of the pathophysiological responses of complex liver diseases. We also discuss how this mechanistic approach can contribute to the discovery of potential biomarkers and novel drug targets, which might lead to the design of targeted and improved treatment strategies. Finally, we present a roadmap for the successful integration of models of the liver and other human tissues with the gut microbiota to simulate whole-body metabolic functions in health and disease.
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