中国临床药理学与治疗学 ›› 2026, Vol. 31 ›› Issue (5): 666-674.doi: 10.12092/j.issn.1009-2501.2026.05.011
收稿日期:2025-04-18
修回日期:2025-06-23
出版日期:2026-05-26
发布日期:2026-06-02
通讯作者:
谭劲
E-mail:liqun@hnucm.edu.cn;tanjinhn@aliyun.com
作者简介:李群,女,在读博士,副主任医师,从事口腔黏膜下纤维化疾病防治研究。E-mail:基金资助:
Qun LI1,2(
), Xinyue ZHANG1, Shuo QI1, Jin TAN1,2,*(
)
Received:2025-04-18
Revised:2025-06-23
Online:2026-05-26
Published:2026-06-02
Contact:
Jin TAN
E-mail:liqun@hnucm.edu.cn;tanjinhn@aliyun.com
摘要:
口腔黏膜下纤维化(oral submucous fibrosis,OSF)是一种常见的口腔疾病,严重影响患者口腔功能与生活质量,且具有一定的癌变风险。转化生长因子-β1(TGF-β1)/Smads信号通路在OSF的发生发展中起着关键作用。中药凭借其多靶点、整体调节的优势,在干预OSF方面展现出一定潜力。本文旨在系统阐述TGF-β1/Smads信号通路在OSF中的作用机制,全面总结中药调控该信号通路干预OSF的研究进展,并对未来研究方向进行展望,为OSF的防治提供参考。
中图分类号:
李群, 张馨月, 祁硕, 谭劲. TGF-β1/Smads信号通路在口腔黏膜下纤维化中的作用机制及中药调控研究进展[J]. 中国临床药理学与治疗学, 2026, 31(5): 666-674.
Qun LI, Xinyue ZHANG, Shuo QI, Jin TAN. Research progress on the mechanism of TGF-β1/Smads signaling pathway in oral submucous fibrosis and regulation of traditional Chinese medicine[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2026, 31(5): 666-674.
| 药物类型 | 具体药物/成分 | 作用机制 | 药效 | 参考文献 |
| 中药单体及提取物 | 表没食子儿茶素没食子酸酯(EGCG) | 抑制TGF-β1相关信号通路,降低 TGF-β1、NO等表达,升高抗氧化酶活性 | 减轻OSF大鼠模型口腔黏膜纤维化程度 | [ |
| 光甘草定 | 抑制TGF-β产生,降低磷酸化Smad2表达,下调 α-SMA和Ⅰ型胶原蛋白 | 抑制人纤维化口腔黏膜成纤维细胞的纤维化相关活动,阻止槟榔碱诱导的成纤维细胞转化 | [ | |
| 槲皮素 | 抑制TGF-β1/Smads 信号通路,降低TGF-β1表达,减少Smad2/3磷酸化 | 抑制槟榔碱诱导的口腔黏膜成 纤维细胞增殖和活化,减少胶原沉积 | [ | |
| 丹参酮 ⅡA1 | 抑制 TGF-β/Smads 通路激活,减少COL1A1、COL3A1等胶原基因转录 | 抑制ANE刺激的小鼠口腔黏膜成纤维细胞异常增殖和胶原积累,改善OSF患者症状 | [ | |
| 姜黄素 | 与TGF-β受体结合,抑制 TGF-β1/Smads信号通路,减少胶原产生 | 抑制肌成纤维细胞增殖,减少胶原合成,改善口腔黏膜病理状态,提高OSF治疗效果 | [ | |
| 蛇床子素 | 抑制TGF-β1/Smad2信号通路,下调NCK1-AS1表达,减少α-SMA和Ⅰ型胶原蛋白 | 降低纤维化口腔黏膜成纤维细胞活力,抑制肌成纤维细胞活性 | [ | |
| 和厚朴酚 | 抑制TGF-β1/Smad2信号通路,减少TGF-β分泌和Smad2磷酸化 | 抑制ANE诱导的肌成纤维细胞活性,缓解OSF进展 | [ | |
| 山竹果皮提取物(含黄蒽酮) | 下调TGF-β/Smad2信号通路相关基因,减少α-SMA和Ⅰ型胶原蛋白表达 | 抑制OSF细胞迁移,诱导细胞凋亡,减轻纤维化 | [ | |
| 中成药 | 复方丹参滴丸 | 通过多种活性成分作用于 TGF-β1信号通路等,抑制纤维化、抗炎、抗氧化 | 联合曲安奈德减轻 OSF患者症状,降低 TGF-β1、IL-6水平 | [ |
| 丹玄口康片 | 调节免疫细胞因子,降低 TGF-β1等促纤维化因子分泌 | 增加OSF大鼠张口度,改善黏膜纤维化症状 | [ | |
| 中药复方 | 玉泉汤加减 | 下调TGF-β1等因子表达,抑制纤维化进程,减轻炎症反应 | 提高OSF癌变干预效果,改善患者临床症状 | [ |
| 利咽解毒方加减 | 下调TGF-β1、CCR2、TLR2 表达,减轻炎症和氧化应激损伤 | 增加患者张口度,缩小病变面积,提高治疗总有效率 | [ |
表 1 中医药调控 TGF-β1/Smads 信号通路治疗口腔黏膜下纤维化的总结
Table 1 Summary of traditional Chinese medicine regulating TGF-β1/Smads signaling pathway in the treatment of oral submucous fibrosis
| 药物类型 | 具体药物/成分 | 作用机制 | 药效 | 参考文献 |
| 中药单体及提取物 | 表没食子儿茶素没食子酸酯(EGCG) | 抑制TGF-β1相关信号通路,降低 TGF-β1、NO等表达,升高抗氧化酶活性 | 减轻OSF大鼠模型口腔黏膜纤维化程度 | [ |
| 光甘草定 | 抑制TGF-β产生,降低磷酸化Smad2表达,下调 α-SMA和Ⅰ型胶原蛋白 | 抑制人纤维化口腔黏膜成纤维细胞的纤维化相关活动,阻止槟榔碱诱导的成纤维细胞转化 | [ | |
| 槲皮素 | 抑制TGF-β1/Smads 信号通路,降低TGF-β1表达,减少Smad2/3磷酸化 | 抑制槟榔碱诱导的口腔黏膜成 纤维细胞增殖和活化,减少胶原沉积 | [ | |
| 丹参酮 ⅡA1 | 抑制 TGF-β/Smads 通路激活,减少COL1A1、COL3A1等胶原基因转录 | 抑制ANE刺激的小鼠口腔黏膜成纤维细胞异常增殖和胶原积累,改善OSF患者症状 | [ | |
| 姜黄素 | 与TGF-β受体结合,抑制 TGF-β1/Smads信号通路,减少胶原产生 | 抑制肌成纤维细胞增殖,减少胶原合成,改善口腔黏膜病理状态,提高OSF治疗效果 | [ | |
| 蛇床子素 | 抑制TGF-β1/Smad2信号通路,下调NCK1-AS1表达,减少α-SMA和Ⅰ型胶原蛋白 | 降低纤维化口腔黏膜成纤维细胞活力,抑制肌成纤维细胞活性 | [ | |
| 和厚朴酚 | 抑制TGF-β1/Smad2信号通路,减少TGF-β分泌和Smad2磷酸化 | 抑制ANE诱导的肌成纤维细胞活性,缓解OSF进展 | [ | |
| 山竹果皮提取物(含黄蒽酮) | 下调TGF-β/Smad2信号通路相关基因,减少α-SMA和Ⅰ型胶原蛋白表达 | 抑制OSF细胞迁移,诱导细胞凋亡,减轻纤维化 | [ | |
| 中成药 | 复方丹参滴丸 | 通过多种活性成分作用于 TGF-β1信号通路等,抑制纤维化、抗炎、抗氧化 | 联合曲安奈德减轻 OSF患者症状,降低 TGF-β1、IL-6水平 | [ |
| 丹玄口康片 | 调节免疫细胞因子,降低 TGF-β1等促纤维化因子分泌 | 增加OSF大鼠张口度,改善黏膜纤维化症状 | [ | |
| 中药复方 | 玉泉汤加减 | 下调TGF-β1等因子表达,抑制纤维化进程,减轻炎症反应 | 提高OSF癌变干预效果,改善患者临床症状 | [ |
| 利咽解毒方加减 | 下调TGF-β1、CCR2、TLR2 表达,减轻炎症和氧化应激损伤 | 增加患者张口度,缩小病变面积,提高治疗总有效率 | [ |
| 1 |
Xu HQ, Guo ZX, Yan JF, et al. Fibrotic matrix induces mesenchymal transformation of epithelial cells in oral submucous fibrosis[J]. Am J Pathol, 2023, 193 (9): 1208- 1222.
doi: 10.1016/j.ajpath.2023.05.014 |
| 2 |
Guo ZX, Zhang Z, Yan JF, et al. A biomaterial-based therapy using a sodium hyaluronate/bioglass composite hydrogel for the treatment of oral submucous fibrosis[J]. Acta Biomater, 2023, 157, 639- 654.
doi: 10.1016/j.actbio.2022.12.006 |
| 3 |
Shen YW, Shih YH, Fuh LJ, et al. Oral submucous fibrosis: a review on biomarkers, pathogenic mechanisms, and treatments[J]. Int J Mol Sci, 2020, 21 (19): 7231.
doi: 10.3390/ijms21197231 |
| 4 |
Phulari RGS, Dave EJ. A systematic review on the mechanisms of malignant transformation of oral submucous fibrosis[J]. Eur J Cancer Prev, 2020, 29 (5): 470- 473.
doi: 10.1097/CEJ.0000000000000575 |
| 5 |
Sacco JL, Vaneman ZT, Gomez EW. Extracellular matrix viscoelasticity regulates TGFβ1-induced epithelial-mesenchymal transition and apoptosis via integrin linked kinase[J]. J Cell Physiol, 2024, 239 (2): e31165.
doi: 10.1002/jcp.31165 |
| 6 |
Moreau JM, Velegrak M, Bolyard C, et al. Transforming growth factor-β1 in regulatory T cell biology[J]. Sci Immunol, 2022, 7 (69): eabi4613.
doi: 10.1126/sciimmunol.abi4613 |
| 7 |
Belair DG, Lee JS, Kellner AV, et al. Receptor mimicking TGF-β1 binding peptide for targeting TGF-β1 signaling[J]. Biomater Sci, 2021, 9 (3): 645- 652.
doi: 10.1039/D0BM01374A |
| 8 |
Xiaojie W, Banda J, Qi H, et al. Scarless wound healing: current insights from the perspectives of TGF-β, KGF-1, and KGF-2[J]. Cytokine Growth Factor Rev, 2022, 66, 26- 37.
doi: 10.1016/j.cytogfr.2022.03.001 |
| 9 |
Miyazawa K, Itoh Y, Fu H, et al. Receptor-activated transcription factors and beyond: multiple modes of Smad2/3-dependent transmission of TGF-β signaling[J]. J Biol Chem, 2024, 300 (5): 107256.
doi: 10.1016/j.jbc.2024.107256 |
| 10 |
Miyazawa K, Miyazono K. Regulation of TGF-β family signaling by inhibitory smads[J]. Cold Spring Harb Perspect Biol, 2017, 9 (3): a022129.
doi: 10.1101/cshperspect.a022095 |
| 11 |
De Ceuninck Van Capelle C, Spit M, Ten Dijke P. Current perspectives on inhibitory SMAD7 in health and disease[J]. Crit Rev Biochem Mol Biol, 2020, 55 (6): 691- 715.
doi: 10.1080/10409238.2020.1828260 |
| 12 |
Tzavlaki K, Moustakas A. TGF-β Signaling[J]. Biomolecules, 2020, 10 (3): 413.
doi: 10.3390/biom10030487 |
| 13 |
Cruz DF, Donovan J, Hejenkowska ED, et al. LMTK2 switches on canonical TGF-β1 signaling in human bronchial epithelial cells[J]. Am J Physiol Lung Cell Mol Physiol, 2024, 327 (5): L769- L782.
doi: 10.1152/ajplung.00034.2024 |
| 14 |
Ning J, Ye Y, Bu D, et al. Imbalance of TGF-β1/BMP-7 pathways induced by M2-polarized macrophages promotes hepatocellular carcinoma aggressiveness[J]. Mol Ther, 2021, 29 (6): 2067- 2087.
doi: 10.1016/j.ymthe.2021.02.016 |
| 15 |
Hu HH, Chen DQ, Wang YN, et al. New insights into TGF-β/Smad signaling in tissue fibrosis[J]. Chem Biol Interact, 2018, 292, 76- 83.
doi: 10.1016/j.cbi.2018.07.008 |
| 16 |
Bijai LK, Muthukrishnan A. Potential role of fibroblast senescence in malignant transformation of oral submucous fibrosis[J]. Oral Oncol, 2022, 127, 105810.
doi: 10.1016/j.oraloncology.2022.105810 |
| 17 |
Wang L, Tang Z. Immunopathogenesis of oral submucous fibrosis by chewing the areca nut[J]. J Leukoc Biol, 2022, 111 (2): 469- 476.
doi: 10.1002/JLB.3MR0521-763RR |
| 18 |
Wang TH, Shen YW, Chen HY, et al. Arecoline induces ROS accumulation, transcription of proinflammatory factors, and expression of KRT6 in oral epithelial cells[J]. Biomedicines, 2024, 12 (2): 324.
doi: 10.3390/biomedicines12020389 |
| 19 |
Zhi Y, Wang Q, Zi M, et al. Spatial transcriptomic and metabolomic landscapes of oral submucous fibrosis-derived oral squamous cell carcinoma and its tumor microenvironment[J]. Adv Sci (Weinh), 2024, 11 (12): e2306515.
doi: 10.1002/advs.202306515 |
| 20 |
Cheng RH, Wang YP, Chang JY, et al. Genetic susceptibility and protein expression of extracellular matrix turnover-related genes in oral submucous fibrosis[J]. Int J Mol Sci, 2020, 21 (21): 8167.
doi: 10.3390/ijms21218148 |
| 21 |
Zhang B, Gao L, Shao C, et al. Arecoline enhances phosphodiesterase 4A activity to promote transforming growth factor-β-induced buccal mucosal fibroblast activation via cAMP-Epac1 signaling pathway[J]. Front Pharmacol, 2021, 12, 722040.
doi: 10.3389/fphar.2021.722040 |
| 22 |
Zhang L, Tan J, Liu YP, et al. Curcumin relieves the arecoline-induced fibrosis of oral mucosal fibroblasts via inhibiting HIF-1α/TGF-β/CTGF signaling pathway: an in vitro study[J]. Toxicol Res (Camb), 2021, 10 (3): 631- 638.
doi: 10.1093/toxres/tfab046 |
| 23 |
Rais A, Husain A, Hasan GM, et al. A review on regulation of cell cycle by extracellular matrix[J]. Int J Biol Macromol, 2023, 232, 123426.
doi: 10.1016/j.ijbiomac.2023.123426 |
| 24 |
Takahashi K, Podyma-Inoue KA, Saito M, et al. TGF-β generates a population of cancer cells residing in G1 phase with high motility and metastatic potential via KRTAP2-3[J]. Cell Rep, 2022, 40 (13): 111411.
doi: 10.1016/j.celrep.2022.111411 |
| 25 |
Hsieh YP, Chen HM, Lin HY, et al. Epigallocatechin-3-gallate inhibits transforming-growth-factor-β1-induced collagen synthesis by suppressing early growth response-1 in human buccal mucosal fibroblasts[J]. J Formos Med Assoc, 2017, 116 (2): 107- 113.
doi: 10.1016/j.jfma.2016.01.014 |
| 26 |
Wang F, Jiang L, Liu P, et al. Mechanism of adipose tissue-derived stromal cell-extracellular vesicles in treating oral submucous fibrosis by blocking the TGF-β1/Smad3 pathway via the miR-760-3p/IGF1R axis[J]. Biomol Biomed, 2023, 24 (4): 827- 839.
doi: 10.17305/bb.2023.9944 |
| 27 |
Shen J, Wang Z, Zhao W, et al. TGF-β1 induces type I collagen deposition in granulosa cells via the AKT/GSK-3β signaling pathway-mediated MMP1 down-regulation[J]. Reprod Biol, 2022, 22 (4): 100705.
doi: 10.1016/j.repbio.2022.100705 |
| 28 |
Shan L, Wang F, Zhai D, et al. Matrix metalloproteinases induce extracellular matrix degradation through various pathways to alleviate hepatic fibrosis[J]. Biomed Pharmacother, 2023, 161, 114472.
doi: 10.1016/j.biopha.2023.114472 |
| 29 |
Derynck R, Muthusamy BP, Saeteurn KY. Signaling pathway cooperation in TGF-β-induced epithelial-mesenchymal transition[J]. Curr Opin Cell Biol, 2014, 31, 56- 66.
doi: 10.1016/j.ceb.2014.09.001 |
| 30 |
Shetty SS, Sharma M, Padam KSR, et al. The interplay of EMT and stemness driving malignant transformation of oral submucous fibrosis[J]. J Oral Biol Craniofac Res, 2024, 14 (1): 63- 71.
doi: 10.1016/j.jobcr.2023.12.006 |
| 31 |
Chatterjee R, Ghosh B, Mandal M, et al. Pathophysiological relationship between hypoxia associated oxidative stress, epithelial-mesenchymal transition, stemness acquisition and alteration of Shh/ Gli-1 axis during oral sub-mucous fibrosis and oral squamous cell carcinoma[J]. Eur J Cell Biol, 2021, 100 (1): 151146.
doi: 10.1016/j.ejcb.2020.151146 |
| 32 |
Ungefroren H. TGF-β signaling in cancer: control by negative regulators and crosstalk with proinflammatory and fibrogenic pathways[J]. Cancers (Basel), 2019, 11 (3): 341.
doi: 10.3390/cancers11030384 |
| 33 |
Chung JY, Chan MK, Li JS, et al. TGF-β signaling: from tissue fibrosis to tumor microenvironment[J]. Int J Mol Sci, 2021, 22 (14): 7563.
doi: 10.3390/ijms22147353 |
| 34 |
Mehta CH, Velagacherla V, Manandhar S, et al. Development of epigallocatechin 3-gallate-loaded hydrogel nanocomposites for oral submucous fibrosis[J]. AAPS PharmSciTech, 2024, 25 (4): 66.
doi: 10.1208/s12249-024-02785-y |
| 35 |
Lee PH, Chu PM, Hsieh PL, et al. Glabridin inhibits the activation of myofibroblasts in human fibrotic buccal mucosal fibroblasts through TGF-β/smad signaling[J]. Environ Toxicol, 2018, 33 (2): 248- 255.
doi: 10.1002/tox.22512 |
| 36 |
Mehta CH, Paliwal S, Muttigi MS, et al. Polyphenol-based targeted therapy for oral submucous fibrosis[J]. Inflammopharmacology, 2023, 31 (5): 2349- 2368.
doi: 10.1007/s10787-023-01212-1 |
| 37 |
Gayathri K, Abhinand PA, Gayathri V, et al. Computational analysis of phytocompounds in Centella asiatica for its antifibrotic and drug-likeness properties - Herb to drug study[J]. Heliyon, 2024, 10 (13): e33762.
doi: 10.1016/j.heliyon.2024.e33762 |
| 38 |
Wu L, Zhang Q, Mo W, et al. Quercetin prevents hepatic fibrosis by inhibiting hepatic stellate cell activation and reducing autophagy via the TGF-β1/Smads and PI3K/Akt pathways[J]. Sci Rep, 2017, 7 (1): 9289.
doi: 10.1038/s41598-017-09673-5 |
| 39 |
Dai JP, Zhu DX, Sheng JT, et al. Inhibition of tanshinone IIA, salvianolic acid A and salvianolic acid B on Areca nut extract-induced oral submucous fibrosis in vitro[J]. Molecules, 2015, 20 (4): 6794- 6807.
doi: 10.3390/molecules20046794 |
| 40 | 李彬彬. 曲安奈德注射液联合丹参酮对口腔黏膜下纤维样变的临床疗效和对血清TGF-β1的影响[J]. 吉林医学, 2022, 43 (4): 997- 998. |
| 41 | 刘彦攀, 蒋健, 戈弋. 丹参酮联合曲安奈德治疗口腔黏膜下纤维化的临床效果[J]. 临床合理用药, 2025, 18 (3): 133- 135. |
| 42 | Rai A, Qazi S, Raza K. In silico analysis and comparative molecular docking study of FDA approved drugs with transforming growth factor beta receptors in oral submucous fibrosis [J]. Indian J Otolaryngol Head Neck Surg, 2022, 74(Suppl 2): 2111-2121. |
| 43 |
Zhang SS, Gong ZJ, Li WH, et al. Antifibrotic effect of curcumin in TGF-β 1-induced myofibroblasts from human oral mucosa[J]. Asian Pac J Cancer Prev, 2012, 13 (1): 289- 294.
doi: 10.7314/APJCP.2012.13.1.289 |
| 44 |
Zeng C, Zhang C, Zhang Y, et al. Formulation, in-vitro characterization and clinical evaluation of curcumin in-situ gel for treatment of oral submucosal fibrosis (OSF)[J]. Int J Pharm, 2025, 679, 125762.
doi: 10.1016/j.ijpharm.2025.125762 |
| 45 |
Gupta S, Ghosh S, Gupta S, et al. Effect of curcumin on the expression of p53, transforming growth factor-β, and inducible nitric oxide synthase in oral submucous fibrosis: a pilot study[J]. J Investig Clin Dent, 2017, 8 (4): e12312.
doi: 10.1111/jicd.12252 |
| 46 |
Yang PY, Hsieh PL, Yeh JC, et al. Osthole mitigates the myofibroblast properties in oral submucous fibrosis by suppressing the TGF-β/smad2 signaling pathway and NCK-AS1 expression[J]. J Dent Sci, 2025, 20 (2): 911- 918.
doi: 10.1016/j.jds.2024.08.021 |
| 47 |
Chen PY, Ho DC, Liao YW, et al. Honokiol inhibits arecoline-induced oral fibrogenesis through transforming growth factor-β/Smad2/3 signaling inhibition[J]. J Formos Med Assoc, 2021, 120 (11): 1988- 1993.
doi: 10.1016/j.jfma.2021.04.012 |
| 48 |
Pj E, Tn U, Perumal E. Inhibition of oral fibrinogenesis through transforming growth factor-beta/SMAD2/3 signalling inhibition using mangosteen pericarp extract[J]. Cureus, 2023, 15 (10): e47899.
doi: 10.7759/cureus.47899 |
| 49 | 张妮. 复方丹参滴丸治疗口腔黏膜下纤维化的作用机制的网络药理学分析及分子对接研究 [D]. 长沙: 湖南中医药大学, 2021. |
| 50 | 罗雪晴, 周文伟. 复方丹参滴丸联合曲安奈德治疗口腔黏膜下纤维性变临床观察[J]. 实用中医药杂志, 2021, 37 (10): 1733- 1735. |
| 51 | 柯云艳, 陈学鹏, 张立港, 等. 复方丹参滴丸联合曲安奈德治疗口腔黏膜下纤维性变的临床观察及对血清TGF-β1、IL-6的影响[J]. 中华中医药学刊, 2019, 37 (8): 1974- 1977. |
| 52 |
谭劲, 岳金宝, 罗玉姣, 等. 丹玄口康对ANE诱导的口腔黏膜下纤维化TGFβ1/Smad信号通路的影响[J]. 中国医药科学, 2018, 8 (5): 27- 31,71.
doi: 10.3969/j.issn.2095-0616.2018.05.009 |
| 53 |
肖艳波, 王宗康, 张琳, 等. 玉泉汤加减对OSF癌变的干预效果及对c-Myc、Cyclin D1、β-catenin表达的影响[J]. 现代生物医学进展, 2020, 20 (8): 1477- 1480,1500.
doi: 10.13241/j.cnki.pmb.2020.08.016 |
| 54 |
张厚华, 沈艳. 玉泉汤联合丹参注射液治疗口腔黏膜下纤维性变疗效及对患者血清白细胞介素6、转化生长因子β1、血液流变学指标的影响[J]. 河北中医, 2018, 40 (3): 353- 357.
doi: 10.3969/j.issn.1002-2619.2018.03.007 |
| 55 | 禹洁, 彭涛, 左巧娟, 等. 利咽解毒方加减对口腔黏膜下纤维化患者CCR2、TLR2水平的影响[J]. 湖南中医药大学学报, 2021, 41 (4): 616- 621. |
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