Network pharmacology‐based identification for therapeutic mechanisms of Dangguikushen pill in acne vulgaris

小桶 痤疮 PI3K/AKT/mTOR通路 计算生物学 药丸 医学 生物途径 Wnt信号通路 信号转导 蛋白激酶B 生物信息学 药理学 传统医学 生物 转录组 基因 遗传学 基因表达 皮肤病科
作者
Bo Yu,Nannan Diao,Ying Zhang,Xing‐Zi Li,Ning Yu,Yang‐Feng Ding,Yuling Shi
出处
期刊:Dermatologic Therapy [Wiley]
卷期号:33 (6) 被引量:4
标识
DOI:10.1111/dth.14061
摘要

The Dangguikushen (DGKS) pill is a proprietary traditional Chinese medicine that has shown superior efficacy in the treatment of acne vulgaris for many years. A network pharmacology-based analysis was performed to explore the potential anti-acne compounds, core therapeutic targets, and the main pathways, involved in the DGKS pill bioactivity. The matching results between the predicted targets of the DGKS pill and the well-known targets of acne vulgaris were collected, followed by network establishment using protein-protein interaction (PPI) data. Cytoscape was utilized to analyze the network and screen the core targets. Furthermore, the Database for Annotation, Visualization and Integrated Discovery (DAVID), and ClueGO were used for the enrichment analysis of the Kyoto Encyclopedia of Genes and Genomics (KEGG) pathways and Gene Ontology biological processes (GO-BP). Finally, the "compound-target-pathway" network was constructed. This approach identified 19 active compounds, 46 therapeutic targets, and 12 core therapeutic targets of the DGKS pill. The biological processes were primarily related to reactive oxygen species (ROS) metabolic process, gland morphogenesis, and female gonad development. The DGKS pill was significantly associated with eight pathways including the PI3K-Akt, TNF, NF-kappa B, and p53 signaling pathways. DGKS pill might have a synergistic effect on the inhibition of excessive sebaceous lipogenesis and sebocyte differentiation, and likewise, anti-inflammatory effects via the different signaling pathways (PI3K-Akt, TNF, NF-kappa B, and p53).
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