Wang Meiwei, He Longmei, Yan Pan
The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410004, Hunan, China.
Department of Pharmacy, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410004, Hunan, China.
Sci Rep. 2025 Feb 15;15(1):5645. doi: 10.1038/s41598-025-90211-z.
Tannic acid (TA) is the primary bioactive component in the gallnut (Galla chinensis) and has exhibited the anticancer effects. However, the mechanism of its anti-cancer activity in nasopharyngeal carcinoma (NPC) remains unclear. This research aims to explore the underlying mechanism of TA in the treatment of nasopharyngeal cancer using network pharmacology, molecular docking and experimental validation. Firstly, the targets of TA and NPC were predicted and collected through databases, and the intersection targets were identified. Subsequently, protein-protein interaction (PPI) network analysis, Gene Ontology (GO) enrichment, Kyoto Encyclopedia of Genes Genomes (KEGG) pathway enrichment analysis, molecular docking and molecular dynamics (MD) simulation were conducted to uncover the potential mechanisms of TA in treatment of NPC. Finally, in vitro experiments were utilized to verify the mechanism of TA with anticancer activity in NPC. The results of network pharmacology revealed 42 intersection targets between NPC-related targets and TA-related targets. The phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) signaling was identified as the main target pathway of TA against NPC. Additionally, molecular docking and MD simulation confirmed the closely binding affinities of TA with AKT1. Furthermore, the results of in vitro experiments demonstrated that TA exerts anticancer activity against NPC by targeting the PI3K/AKT signaling pathway, leading to the suppression of cell proliferation. TA is a promising therapeutic candidate for NPC through PI3K/AKT signaling pathway. These results provide insights into the clinical application of TA, particularly when considered in combination with other therapeutic modalities.
单宁酸(TA)是五倍子(没食子)中的主要生物活性成分,并已显示出抗癌作用。然而,其在鼻咽癌(NPC)中的抗癌活性机制仍不清楚。本研究旨在利用网络药理学、分子对接和实验验证来探索TA治疗鼻咽癌的潜在机制。首先,通过数据库预测并收集TA和NPC的靶点,并确定交集靶点。随后,进行蛋白质-蛋白质相互作用(PPI)网络分析、基因本体(GO)富集、京都基因与基因组百科全书(KEGG)通路富集分析、分子对接和分子动力学(MD)模拟,以揭示TA治疗NPC的潜在机制。最后,利用体外实验验证TA在NPC中具有抗癌活性的机制。网络药理学结果显示,NPC相关靶点与TA相关靶点之间有42个交集靶点。磷酸肌醇3-激酶(PI3K)/蛋白激酶B(AKT)信号通路被确定为TA抗NPC的主要靶点途径。此外,分子对接和MD模拟证实了TA与AKT1具有紧密的结合亲和力。此外,体外实验结果表明,TA通过靶向PI3K/AKT信号通路发挥对NPC的抗癌活性,从而抑制细胞增殖。通过PI3K/AKT信号通路,TA是一种有前景的NPC治疗候选药物。这些结果为TA的临床应用提供了见解,特别是当与其他治疗方式联合考虑时。