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Deciphering the Potential Pharmaceutical Mechanism of GUI-ZHI-FU-LING-WAN on Systemic Sclerosis based on Systems Biology Approaches

机译:基于系统生物学方法的桂枝FU灵丸对系统性硬化的潜在药物作用机理的研究

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Systemic sclerosis (SSc; scleroderma) is a complicated idiopathic connective tissue disease with seldom effective treatment. GUI-ZHI-FU-LING-WAN (GFW) is a classic Traditional Chinese Medicine (TCM) formula widely used for the treatment of SSc. However, the mechanism of how the GFW affects SSc remains unclear. In this study, the system biology approach was utilized to analyze herb compounds and related targets to get the general information of GFW. The KEGG enrichment analysis of 1645 related targets suggested that the formula is involved in the VEGF signaling pathway, the Toll-like receptor signaling pathway, etc. Quantitative and qualitative analysis of the relationship among the 3 subsets (formula targets, drug targets and disease genes) showed that the formula targets overlapped with 38.0% drug targets and 26.0% proteins encoded by disease genes. Through the analysis of SSc related microarray statistics from the GEO database, we also validated the consistent expression behavior among the 3 subsets before and after treatment. To further reveal the mechanism of prescription, we constructed a network among 3 subsets and decomposed it into 24 modules to decipher how GFW interfere in the progress of SSc. The modules indicated that the intervention may come into effect through following pathogenic processes: vasculopathy, immune dysregulation and tissue fibrosis. Vitro experiments confirmed that GFW could suppress the proliferation of fibroblasts and decrease the Th1 cytokine (TNF-α, MIP-2 and IL-6) expression for lipopolysaccharide (LPS) and bleomycin (BLM) stimulation in macrophages, which is consistent with previous conclusion that GFW is able to relieve SSc. The systems biology approach provides a new insight for deepening understanding about TCM.
机译:系统性硬化症(SSc;硬皮病)是一种复杂的特发性结缔组织病,很少有效治疗。桂枝附灵丸(GFW)是经典的中药(TCM)配方,广泛用于SSc的治疗。但是,GFW如何影响SSc的机制仍不清楚。在这项研究中,系统生物学方法被用来分析草药化合物和相关目标,以获得GFW的一般信息。 KEGG对1645个相关靶标的富集分析表明,该公式参与了VEGF信号传导途径,Toll样受体信号传导途径等。定量和定性分析了3个子集(配方靶标,药物靶标和疾病基因)之间的关系。 )显示,配方目标与疾病基因编码的38.0%药物目标和26.0%蛋白质重叠。通过从GEO数据库中分析与SSc相关的微阵列统计数据,我们还验证了治疗前后3个子集中一致的表达行为。为了进一步揭示处方机制,我们在3个子集中构建了一个网络,并将其分解为24个模块,以了解GFW如何干扰SSc的进程。这些模块表明,该干预措施可能通过以下致病过程生效:血管病变,免疫失调和组织纤维化。体外实验证实,GFW可以抑制巨噬细胞中脂多糖(LPS)和博来霉素(BLM)刺激的成纤维细胞增殖并降低Th1细胞因子(TNF-α,MIP-2和IL-6)的表达,这与先前的结论一致GFW能够缓解SSc。系统生物学方法为加深对中医的理解提供了新的见解。

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