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    基于网络药理学研究新“浙八味”衢枳壳黄酮抗肝细胞癌的作用机制

    Study on the Mechanism of the Flavonoids from the New "Zhe Eight Flavors" Quzhou Fructus Aurantii Against Hepatocellular Carcinoma Based on Network Pharmacology

      摘要
    • 摘要:
      目的  基于网络药理学预测并通过实验验证新“浙八味”衢枳壳黄酮类活性成分抗肝细胞癌的作用机制。
      方法 通过TCMSP、TCMID、ETCM、BATMAN-TCM及SwissTargetPrediction数据库收集衢枳壳黄酮类化合物(包括柚皮苷、芸香柚皮苷、新橙皮苷)的潜在作用靶点；应用GeneCards、CTD、Disgenet和OMIM数据库构建肝细胞癌疾病靶点集；将衢枳壳黄酮潜在靶点与肝细胞癌靶点取交集以获取关键靶点蛋白，建立蛋白互作网络；对核心靶点进行GO 功能和KEGG 通路富集分析，并构建成分-靶点-通路-疾病网络；采用增殖、克隆、愈合与迁移试验分析衢枳壳黄酮对肝癌细胞HepG2活力的影响；使用荧光探针染色观察衢枳壳黄酮对HepG2细胞线粒体膜电位与凋亡的影响；运用RT-qPCR技术验证衢枳壳黄酮对网络药理学预测的关键靶点PRKCA的调控作用。
      结果 基于网络药理学筛选得到217个衢枳壳黄酮的作用靶点，与疾病靶点的交集靶点59个，涉及ALB、ESR1、PRKCA等。GO 功能与KEGG 通路富集分析显示，衢枳壳黄酮作用靶点共涉及193个生物学过程，13条癌症相关信号通路。实验结果表明衢枳壳黄酮能影响肝癌细胞的增殖、克隆、愈合与迁移能力，导致线粒体膜电位下降并促进细胞凋亡。RT-qPCR的结果表明衢枳壳黄酮能够显著下调PRKCA表达，验证了网络药理学的预测分析结果。
      结论 本研究揭示了衢枳壳黄酮通过PRKCA靶点治疗肝细胞癌的潜在分子作用机制，为其临床防治肝细胞癌的应用奠定基础。

       

      Abstract:
      OBJECTIVE  To explore the mechanisms of the flavonoids from new "Zhe Eight Flavors" Quzhou Fructus Aurantii(PTFC) against hepatocellular carcinoma based on the prediction of network pharmacology and experimental verification.
      METHODS  From TCMSP, TCMID, ETCM, BATMAN-TCM and SwissTargetPrediction databases, the potential target proteins of PTFC, including naringin, narirutin and neohesperidin were collected. Based on the GeneCards, CTD, Disgenet, and OMIM databases, a set of target proteins for hepatocellular carcinoma was constructed. Taking the intersection of potential target proteins of PTFC and target proteins of hepatocellular carcinoma, key target proteins were obtained and a protein-protein interaction network was established. Besides, GO function and KEGG pathway enrichment analysis on the core target proteins was performed and a Compounds-Targets-Pathways-Disease network was constructed. Through proliferation, cloning, wound healing, and migration experiments, the effects of PTFC on the viability of HepG2 liver cancer cells were analyzed. Using fluorescence probe staining the impacts of PTFC on the mitochondrial membrane potential and apoptosis of HepG2 were observed. Finally, the validation of the regulatory effect of PTFC on the key predicted target PRKCA were carried out through RT-qPCR.
      RESULTS Based on network pharmacology, a total of 217 potential target proteins for PTFC were screened, with 59 intersecting target proteins related to diseases, including ALB, ESR1, PRKCA, and others. GO functional and KEGG pathway enrichment analysis revealed that the PTFC target proteins were involved in 193 biological processes and 13 cancer-related signaling pathways. Experimental results demonstrated that PTFC could impact the proliferation, cloning, wound healing, and migration abilities of liver cancer cells, leading to a decrease in mitochondrial membrane potential and promoting cell apoptosis. The results of RT-qPCR confirmed a significant downregulation of PRKCA expression by PTFC, validating the predictions made by network pharmacology analysis.
      CONCLUSION  This study has revealed the potential molecular mechanism of PTFC treating hepatocellular carcinoma via the PRKCA target, laying the foundation for clinical application of PTFC.

       

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