基于网络药理学探究三棱–莪术治疗甲状腺结节的作用机制
Exploring the Mechanism of Sanleng-Ezhu in Treating Thyroid Nodules Based on Network Pharmacology
摘要: 目的:采用网络药理学方法研究三棱与莪术干预甲状腺结节的作用机理。方法:检索TCMSP数据库获取三棱与莪术的活性成分,再利用Uniprot数据库获得三棱与莪术标准化的靶点数据。借助Genecard数据库以及OMIM数据库查询收集甲状腺结节的相关靶点数据,并通过韦恩图平台获得甲状腺结节与三棱、莪术之间的共同基因。通过Cytoscape软件建立三棱、莪术活性成分–靶点网络信息图谱,并使用STRING数据库构建PPI网络模型,进而对关键靶点开展GO功能富集分析和KEGG通路富集分析。结果:三棱–莪术药对筛选得出5个有效活性成分,药物靶点69个。甲状腺结节疾病相关靶点4267个,疾病与药物交集靶点44个。PPI网络模型分析得到三棱–莪术治疗甲状腺结节以PTGS2、PPARG、BCL2、CASP3、ESR1为核心靶点。GO功能富集分析结果表明,潜在治疗靶点主要介入了对雌二醇的应答、低氧反应、核受体介导的信号通路等生物过程;KEGG通路富集分析显示,三棱–莪术干预甲状腺结节所涉及到的通路主要涵盖p53信号通路、甲状腺激素信号通路、IL-17信号通路、PI3K-Akt信号通路等。结论:三棱–莪术药对可依靠若干靶点以及多条通路的协同效应,实现对甲状腺结节的治疗作用。
Abstract: Objective: To explore the mechanism by which Sanleng (Sparganium stoloniferum) and Ezhu (Curcuma phaeocaulis) intervene in thyroid nodules using a network pharmacology approach. Methods: Active components of Sanleng and Ezhu were retrieved from the TCMSP database, and their standardized target data were subsequently obtained from the UniProt database. The Genecards and OMIM databases were searched to collect target information associated with thyroid nodules, and a Venn diagram platform was used to identify common genes shared between thyroid nodule targets and those of Sanleng and Ezhu. Cytoscape software was employed to construct an active component-target network map for the two herbs, and the STRING database was utilized to build a protein-protein interaction (PPI) network model. GO functional enrichment analysis and KEGG pathway enrichment analysis were then conducted on the key targets. Results: Screening of the Sanleng-Ezhu herb pair identified 5 effective active components and 69 drug-related targets. A total of 4267 disease-related targets for thyroid nodules were found, with 44 overlapping targets between the disease and the herbs. PPI network analysis indicated that the core therapeutic targets of Sanleng-Ezhu for treating thyroid nodules are PTGS2, PPARG, BCL2, CASP3, and ESR1. GO functional enrichment analysis showed that the potential therapeutic targets are primarily involved in biological processes such as response to estradiol, response to hypoxia, and nuclear receptor-mediated signaling pathway; KEGG pathway enrichment analysis revealed that the pathways implicated in Sanleng-Ezhu intervention in thyroid nodules mainly include the p53 signaling pathway, thyroid hormone signaling pathway, IL-17 signaling pathway, and PI3K-Akt signaling pathway, among others. Conclusion: The Sanleng-Ezhu herb pair may achieve therapeutic effects against thyroid nodules through the synergistic actions of multiple targets and several signaling pathways.
文章引用:文冰冰. 基于网络药理学探究三棱–莪术治疗甲状腺结节的作用机制[J]. 中医学, 2026, 15(1): 281-289. https://doi.org/10.12677/tcm.2026.151040

参考文献

[1] 徐志伟, 李秀萍, 庄道平. 针药并用治疗甲状腺结节的疗效观察[J]. 上海针灸杂志, 2025, 44(8): 936-941.
[2] Studen, K.B., Domagała, B., Gaberšček, S., Zaletel, K. and Hubalewska-Dydejczyk, A. (2024) Diagnosing and Management of Thyroid Nodules and Goiter—Current Perspectives. Endocrine, 87, 39-47. [Google Scholar] [CrossRef] [PubMed]
[3] 贾春艳, 张兰. 甲状腺结节的中西医治疗研究进展[J]. 湖南中医杂志, 2024, 40(8): 203-207.
[4] 高天舒, 倪青. 甲状腺结节病证结合诊疗指南(2022) [J]. 中医杂志, 2023, 64(4): 425-432.
[5] 徐永军, 张志玲, 陈宏. 中医药治疗甲状腺结节的现状与展望[J]. 中医药学报, 2024, 52(4): 85-90.
[6] 王惠茹, 梁爽, 张骞, 等. 原发性肝癌中活血化瘀类常用中药的成分及作用分析[J]. 中国医药科学, 2024, 14(8): 45-48.
[7] 唐荣霜, 石洲, 李晋奇, 等. 三棱莪术药对的研究进展[J]. 实用医院临床杂志, 2021, 18(5): 226-229.
[8] Wang, W., Jin, Y., Liu, M., Zhang, S., Chen, H. and Song, J. (2025) Current Progress of Hederagenin and Its Derivatives for Disease Therapy (2017-Present). Molecules, 30, Article No. 1275. [Google Scholar] [CrossRef] [PubMed]
[9] Wen, Y., Pang, L., Fan, L., Zhou, Y., Li, R., Zhao, T. and Zhang, M. (2023) β-Sitosterol Inhibits the Proliferation of Endometrial Cells via Regulating Smad7-Mediated TGF-β/Smads Signaling Pathway. Cell, 25, 554-563.
[10] Jin, M., Wei, L., Wang, J., Shen, Y., Gao, L., Zhao, F., et al. (2025) Formononetin: A Review of Its Source, Pharmacology, Drug Combination, Toxicity, Derivatives, and Drug Delivery Systems. Frontiers in Pharmacology, 16, Article ID: 1534798. [Google Scholar] [CrossRef] [PubMed]
[11] Valitova, J., Renkova, A., Beckett, R. and Minibayeva, F. (2024) Stigmasterol: An Enigmatic Plant Stress Sterol with Versatile Functions. International Journal of Molecular Sciences, 25, Article No. 8122. [Google Scholar] [CrossRef] [PubMed]
[12] Jin, G., Xu, W., Tang, H., Cui, Y. and Zhang, H. (2024) Bisdemethoxycurcumin, a Curcumin, Protects Chondrocytes, and Reduces Cartilage Inflammation via the NRF2/HO‐1/NLRP3 Pathway. Immunity, Inflammation and Disease, 12, e1195. [Google Scholar] [CrossRef] [PubMed]
[13] Al-Maghrabi, J. and Gomaa, W. (2022) High COX-2 Immunostaining in Papillary Thyroid Carcinoma Is Associated with Adverse Survival Outcomes. Annals of Saudi Medicine, 42, 359-365. [Google Scholar] [CrossRef] [PubMed]
[14] Nam, S.M., Kim, J.W., Yoo, D.Y., Jung, H.Y., Chung, J.Y., Kim, D.W., et al. (2018) Hypothyroidism Increases Cyclooxygenase-2 Levels and Pro-Inflammatory Response and Decreases Cell Proliferation and Neuroblast Differentiation in the Hippocampus. Molecular Medicine Reports, 17, 5782-5788. [Google Scholar] [CrossRef] [PubMed]
[15] 贺旸知歌, 姜旭, 张志文, 等. PTGS2调控细胞增殖及抗氧化能力影响结肠癌患者预后[J]. 基础医学与临床, 2024, 44(11): 1522-1529.
[16] 贠浩, 周锦纹, 张锋, 等. 敲减PPARG对乳腺癌MCF-7细胞裸鼠移植瘤生长影响的研究[J]. 中国现代普通外科进展, 2023, 26(2): 89-92+110.
[17] Wang, H., Guo, M., Wei, H. and Chen, Y. (2023) Targeting p53 Pathways: Mechanisms, Structures and Advances in Therapy. Signal Transduction and Targeted Therapy, 8, Article No. 92. [Google Scholar] [CrossRef] [PubMed]
[18] Thibault, B., Ramos-Delgado, F. and Guillermet-Guibert, J. (2023) Targeting Class I-II-III PI3Ks in Cancer Therapy: Recent Advances in Tumor Biology and Preclinical Research. Cancers, 15, Article No. 784. [Google Scholar] [CrossRef] [PubMed]
[19] Shariati, M. and Meric-Bernstam, F. (2019) Targeting AKT for Cancer Therapy. Expert Opinion on Investigational Drugs, 28, 977-988. [Google Scholar] [CrossRef] [PubMed]
[20] Brzezianska, E. and Pastuszak-Lewandoska, D. (2011) A Minireview: The Role of MAPK/ERK and PI3K/Akt Pathways in Thyroid Follicular Cell-Derived Neoplasm. Frontiers in Bioscience, 16, 422-439. [Google Scholar] [CrossRef] [PubMed]