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基于动态网络生物标志物检测复杂疾病的组织特异性早期预警信号:通过跨组织分析研究2型糖尿病

Detecting tissue-specific early warning signals for complex diseases based on dynamical network biomarkers: study of type 2 diabetes by cross-tissue analysis.

作者信息

Li Meiyi, Zeng Tao, Liu Rui, Chen Luonan

机构信息

Key Laboratory of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031, China. Tel.: +86 21-5492-0100; Fax: +86 21-5497-2551;

出版信息

Brief Bioinform. 2014 Mar;15(2):229-43. doi: 10.1093/bib/bbt027. Epub 2013 Apr 25.

Abstract

Identifying early warning signals of critical transitions during disease progression is a key to achieving early diagnosis of complex diseases. By exploiting rich information of high-throughput data, a novel model-free method has been developed to detect early warning signals of diseases. Its theoretical foundation is based on dynamical network biomarker (DNB), which is also called as the driver (or leading) network of the disease because components or molecules in DNB actually drive the whole system from one state (e.g. normal state) to another (e.g. disease state). In this article, we first reviewed the concept and main results of DNB theory, and then applied the new method to the analysis of type 2 diabetes mellitus (T2DM). Specifically, based on the temporal-spatial gene expression data of T2DM, we identified tissue-specific DNBs corresponding to the critical transitions occurring in liver, adipose and muscle during T2DM development and progression. Actually, we found that there are two different critical states during T2DM development characterized as responses to insulin resistance and serious inflammation, respectively. Interestingly, a new T2DM-associated function, i.e. steroid hormone biosynthesis, was discovered, and those related genes were significantly dysregulated in liver and adipose at the first critical transition during T2DM deterioration. Moreover, the dysfunction of genes related to responding hormone was also detected in muscle at the similar period. Based on the functional and network analysis on pathogenic molecular mechanism of T2DM, we showed that most of DNB genes, in particular the core ones, tended to be located at the upstream of biological pathways, which implied that DNB genes act as the causal factors rather than the consequence to drive the downstream molecules to change their transcriptional activities. This also validated our theoretical prediction of DNB as the driver network. As shown in this study, DNB can not only signal the emergence of the critical transitions for early diagnosis of diseases, but can also provide the causal network of the transitions for revealing molecular mechanisms of disease initiation and progression at a network level.

摘要

识别疾病进展过程中关键转变的早期预警信号是实现复杂疾病早期诊断的关键。通过利用高通量数据的丰富信息,已开发出一种新型的无模型方法来检测疾病的早期预警信号。其理论基础基于动态网络生物标志物(DNB),它也被称为疾病的驱动(或主导)网络,因为DNB中的成分或分子实际上驱动整个系统从一种状态(如正常状态)转变为另一种状态(如疾病状态)。在本文中,我们首先回顾了DNB理论的概念和主要成果,然后将该新方法应用于2型糖尿病(T2DM)的分析。具体而言,基于T2DM的时空基因表达数据,我们识别出了与T2DM发生和发展过程中肝脏、脂肪和肌肉中发生的关键转变相对应的组织特异性DNB。实际上,我们发现T2DM发展过程中有两种不同的关键状态,分别表现为对胰岛素抵抗和严重炎症的反应。有趣的是,发现了一种新的与T2DM相关的功能,即类固醇激素生物合成,并且在T2DM恶化的第一个关键转变期间,这些相关基因在肝脏和脂肪中显著失调。此外,在同一时期的肌肉中也检测到了与激素反应相关基因的功能障碍。基于对T2DM致病分子机制的功能和网络分析,我们表明大多数DNB基因,特别是核心基因,倾向于位于生物途径的上游,这意味着DNB基因作为因果因素而非结果来驱动下游分子改变其转录活性。这也验证了我们将DNB作为驱动网络的理论预测。如本研究所示,DNB不仅可以为疾病的早期诊断发出关键转变出现的信号,还可以提供转变的因果网络,以便在网络层面揭示疾病发生和发展的分子机制。

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