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基于网络药理学阐明双联方治疗肝细胞癌的作用机制及分子靶点

Elucidation of the Mechanisms and Molecular Targets of Shuanglian Decoction for the Treatment of Hepatocellular Carcinoma Based on Network Pharmacology.

作者信息

He Kun, Chen Hua, Cao Tianshou, Lin Jiantao

机构信息

Hepatobiliary Surgery, Zhongshan People's Hospital, Zhongshan 528403, China.

The Second Tumor Department, Maoming People's Hospital, Maoming 525000, China.

出版信息

ACS Omega. 2020 Dec 31;6(1):917-924. doi: 10.1021/acsomega.0c05550. eCollection 2021 Jan 12.

Abstract

Shuanglian decoction (SLD) is traditionally used to treat hepatocellular carcinoma (HCC) in the clinical practice of traditional Chinese medicine. However, its mechanisms of action and molecular targets for the treatment of HCC are not clear. The active compounds of SLD were collected and their targets were identified. HCC-related targets were obtained by analyzing the differentially expressed genes between HCC patients and healthy individuals. Protein-protein interaction (PPI) data were then obtained and PPI networks of SLD putative targets and HCC-related targets were visualized and merged to identify the candidate targets for SLD against HCC. Gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis were carried out. The gene-pathway network was constructed to screen the key target genes. In total, 35 active compounds and 31 targets of SLD were identified. In total, 245 differentially expressed genes with values <0.005 and |log2 (fold change)| > 1 were identified between HCC patients and control groups, and 68 target genes associated with HCC were finally identified. Twenty-one pathways including cellular senescence, p53 signaling pathway, and cell cycle were significantly enriched. CYP3A4 was the core gene and other several genes including CYP1A2, PPP3CA, PTGS2, CCCNB1, and CDK1 were the key genes in the gene-pathway network of SLD for the treatment of HCC. The results indicated that SLD's effects against HCC may relate to the regulation of an antioxidant function through specific biological processes and related pathways. This study demonstrates the application of network pharmacology in evaluating mechanisms of action and molecular targets of complex herbal formulations.

摘要

双联汤(SLD)在中医临床实践中传统上用于治疗肝细胞癌(HCC)。然而,其治疗HCC的作用机制和分子靶点尚不清楚。收集了SLD的活性成分并鉴定了其靶点。通过分析HCC患者与健康个体之间的差异表达基因获得HCC相关靶点。然后获取蛋白质-蛋白质相互作用(PPI)数据,并将SLD假定靶点和HCC相关靶点的PPI网络可视化并合并,以确定SLD抗HCC的候选靶点。进行了基因本体论和京都基因与基因组百科全书通路分析。构建基因-通路网络以筛选关键靶基因。共鉴定出35种SLD的活性成分和31个靶点。在HCC患者与对照组之间共鉴定出245个差异表达基因,其值<0.005且|log2(倍数变化)|>1,最终鉴定出68个与HCC相关的靶基因。包括细胞衰老、p53信号通路和细胞周期在内的21条通路显著富集。CYP3A4是核心基因,包括CYP1A2、PPP3CA、PTGS2、CCCNB1和CDK1在内的其他几个基因是SLD治疗HCC的基因-通路网络中的关键基因。结果表明,SLD对HCC的作用可能与通过特定生物学过程和相关通路调节抗氧化功能有关。本研究证明了网络药理学在评估复杂草药制剂作用机制和分子靶点方面的应用。

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