Nie Wenna, Lv Yana, Yan Leyu, Chen Xi, Lv Haitao
Chongqing University Innovative Drug Research Centre, School of Chemistry and Chemical Engineering, Chongqing 401331, P.R. China.
Yunnan Branch, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Jinghong 666100, P.R China.
Sci Rep. 2015 Dec 1;5:17646. doi: 10.1038/srep17646.
Aristolochic acid (AA) is the major active component of medicinal plants from the Aristolochiaceae family of flowering plants widely utilized for medicinal purposes. However, the molecular mechanisms of AA systems effects remain poorly understood. Here, we employed a joint network analysis that combines network pharmacology, a protein-protein interaction (PPI) database, biological processes analysis and functional annotation analysis to explore system effects. Firstly, we selected 15 protein targets (14 genes) in the PubChem database as the potential target genes and used PPI knowledge to incorporate these genes into an AA-specific gene network that contains 129 genes. Secondly, we performed biological processes analysis for these AA-related targets using ClueGO, some of new targeted genes were randomly selected and experimentally verified by employing the Quantitative Real-Time PCR assay for targeting the systems effects of AA in HK-2 cells with observed dependency of concentration. Thirdly, the pathway-based functional enrichment analysis was manipulated using WebGestalt to identify the mostly significant pathways associated with AA. At last, we built an AA target pathway network of significant pathways to predict the system effects. Taken together, this joint network analysis revealed that the systematic regulatory effects of AA on multidimensional pathways involving both therapeutic action and toxicity.
马兜铃酸(AA)是马兜铃科开花植物中广泛用于药用的药用植物的主要活性成分。然而,AA系统效应的分子机制仍知之甚少。在此,我们采用了一种联合网络分析方法,该方法结合了网络药理学、蛋白质-蛋白质相互作用(PPI)数据库、生物学过程分析和功能注释分析来探索系统效应。首先,我们在PubChem数据库中选择了15个蛋白质靶点(14个基因)作为潜在靶基因,并利用PPI知识将这些基因纳入一个包含129个基因的AA特异性基因网络。其次,我们使用ClueGO对这些与AA相关的靶点进行生物学过程分析,随机选择一些新的靶向基因,并通过定量实时PCR检测对其进行实验验证,以观察AA在HK-2细胞中的系统效应与浓度的相关性。第三,使用WebGestalt进行基于通路的功能富集分析,以确定与AA相关的最显著通路。最后,我们构建了一个由显著通路组成的AA靶标通路网络,以预测系统效应。综上所述,这种联合网络分析表明,AA对涉及治疗作用和毒性的多维通路具有系统性调节作用。