基于网络药理学分析的肾病综合征治疗新前景

IF 2.1 Q3 PHYSIOLOGY
Rini Varghese, Anuradha Majumdar
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引用次数: 5

摘要

网络药理学是一个新兴的领域,目前正在引起人们对药物发现和开发的兴趣。慢性肾脏疾病已成为一个全球性的威胁,由于其相关的终身治疗。肾病综合征(NS)是一种常见于儿童和成人的肾小球疾病,特征性表现为蛋白尿、水肿、低白蛋白血症和高脂血症。它包括足细胞损伤伴小管间质纤维化和肾小球硬化。到目前为止,还没有专门的治疗方法可以完全缓解这种情况。因此,药物再利用可能是治疗NS的一种潜在策略。最近,发现了促进许多肾脏疾病进展的表观遗传机制。因此,在本研究中,我们研究了两种表观遗传药物丙戊酸(VPA)和全反式维甲酸(ATRA)。表观遗传药物的作用是在不改变DNA序列的情况下改变基因表达。这些变化包括DNA甲基化或组蛋白修饰。ATRA和VPA两种药物的靶点从ChEMBL和Binding DB中整理。所有与NS相关的基因均从DisGeNET和KEGG数据库中收集。目的基因的相互作用蛋白从STRING数据库中获取。然后使用功能富集软件工具对这些基因进行基因本体和途径富集分析。利用Cytoscape软件构建药物靶点和药物潜在靶点-蛋白相互作用网络。我们的研究结果显示,VPA和ATRA这两种药物有65个共同的靶点,导致肾脏疾病。其中25个靶点与NS特异性相关。此外,我们的研究表明,ATRA和VPA协同参与炎症、肾纤维化、肾小球硬化和可能的线粒体生物发生和内质网应激的途径。因此,我们提出两种药物在治疗慢性肾脏疾病,特别是NS方面具有协同潜力。这些结果无疑将为进一步的临床前和临床探索性研究注入活力。我们将网络药理学确定为确定候选药物重新利用和协同作用的初始固有方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A New Prospect for the Treatment of Nephrotic Syndrome Based on Network Pharmacology Analysis

A New Prospect for the Treatment of Nephrotic Syndrome Based on Network Pharmacology Analysis

Network pharmacology is an emerging field which is currently capturing interest in drug discovery and development. Chronic kidney conditions have become a threat globally due to its associated lifelong therapies. Nephrotic syndrome (NS) is a common glomerular disease that is seen in paediatric and adult population with characteristic manifestation of proteinuria, oedema, hypoalbuminemia, and hyperlipidemia. It involves podocyte damage with tubulointerstitial fibrosis and glomerulosclerosis. Till date there has been no specific treatment available for this condition that provides complete remission. Repurposing of drugs can thus be a potential strategy for the treatment of NS. Recently, epigenetic mechanisms were identified that promote progression of many renal diseases. Therefore, in the present study, we investigated two epigenetic drugs valproic acid (VPA) and all-trans retinoic acid (ATRA). Epigenetic drugs act by binging about changes in gene expression without altering the DNA sequence. The changes include DNA methylation or histone modifications. The targets for the two drugs ATRA and VPA were collated from ChEMBL and Binding DB. All the genes associated with NS were collected from DisGeNET and KEGG database. Interacting proteins for the target genes were acquired from STRING database. The genes were then subjected to gene ontology and pathway enrichment analysis using a functional enrichment software tool. A drug-target and drug-potential target-protein interaction network was constructed using the Cytoscape software. Our results revealed that the two drugs VPA and ATRA had 65 common targets that contributed to kidney diseases. Out of which, 25 targets were specifically NS associated. Further, our work exhibited that ATRA and VPA were synergistically involved in pathways of inflammation, renal fibrosis, glomerulosclerosis and possibly mitochondrial biogenesis and endoplasmic reticulum stress. We thus propose a synergistic potential of the two drugs for treating chronic kidney diseases, specifically NS. The outcomes will undoubtedly invigorate further preclinical and clinical explorative studies. We identify network pharmacology as an initial inherent approach in identifying drug candidates for repurposing and synergism.

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