中国实用口腔科杂志 ›› 2026, Vol. 19 ›› Issue (1): 10-18.DOI: 10.19538/j.kq.2026.01.002

• 专题笔谈 • 上一篇    下一篇

放射性口腔黏膜炎的小分子靶向药物研发

蒋    琴,周    刚   

  1. 武汉大学口腔医院口腔黏膜科,口颌系统重建与再生全国重点实验室,口腔生物医学教育部重点实验室,口腔医学湖北省重点实验室,湖北 武汉 430079
  • 出版日期:2026-01-30 发布日期:2026-01-30
  • 通讯作者: 周刚
  • 作者简介:周刚,教授、一级主任医师、博士研究生导师。现任武汉大学口腔医院口腔黏膜科主任。兼任中华口腔医学会第八届口腔黏膜病学专业委员会主任委员,湖北省口腔医学会口腔黏膜病及中西医结合专业委员会主任委员,国际牙医师学院(ICD)院士,湖北省专项津贴专家。主持国家自然科学基金面上项目8项、省部级项目10余项。在国内外发表论文170余篇。主编《口腔黏膜病临床病例精解》《口腔黏膜病药物治疗精解》等专著5部,副主编3部,参编欧洲Diseases of the Oral Mucosa、全国高等学校本科生及研究生规划教材《口腔黏膜病学》等专著30余部,牵头制定本行业3个诊疗指南及专家共识。
  • 基金资助:
    四大慢病重大专项(2023ZD0503000)

  • Online:2026-01-30 Published:2026-01-30

摘要: 放射性口腔黏膜炎(radiation-induced oral mucositis,RIOM)是头颈部肿瘤放疗过程中常见且严重的并发症,其发病机制涉及氧化应激、炎症反应、免疫激活及上皮修复障碍等多个环节。目前RIOM的临床干预手段有限,缺乏针对其病理机制的特异性治疗药物。近年来,以小分子靶向药物为核心的RIOM干预策略逐渐成为研究热点。文章针对RIOM不同病理阶段的小分子靶向药物[包括靶向氧化应激的超氧化物歧化酶模拟物和核因子红细胞2相关因子2(nuclear factor erythroid 2-related factor 2,Nrf2)调节剂、调控固有免疫应答的先天防御调节剂、抑制关键炎症通路的核因子κB(nuclear factor κB,NF-κB)抑制剂及促进黏膜上皮修复的尿苷磷酸化酶抑制剂等]进行系统综述,阐述相应药物的作用机制,总结其临床前及临床研究进展,并分析当前研发过程中面临的关键挑战,展望未来多靶点联合用药等的发展方向,以期为RIOM的精准防治提供理论依据和策略支持。

关键词: 放射性口腔黏膜炎, 小分子靶向药物, 氧化应激, 炎症反应, 临床试验

Abstract: Radiation-induced oral mucositis(RIOM)is a common and severe complication of radiotherapy for head and neck cancers. Its pathogenesis involves multiple processes,including oxidative stress,inflammatory response,immune activation,and impaired epithelial repair. Currently,clinical interventions for RIOM have limited efficacy,and there is a lack of specific therapeutic drugs targeting the underlying pathological mechanisms. In recent years,the intervention strategies for RIOM with small-molecule targeted drugs as the core have gradually become a research focus. This article systematically reviews small-molecule targeted drugs acting across various pathological stages of RIOM,including superoxide dismutase mimetics and nuclear factor erythroid 2-related factor 2(Nrf2)modulators that target oxidative stress,innate defense regulators that modulate innate immunity,nuclear factor κB(NF-κB)inhibitors that suppress key inflammatory pathway,and uridine phosphorylase inhibitors that promote mucosal epithelial repair,elaborating on their mechanisms of action,summarizing the preclinical and clinical research progress,and analyzing key challenges in current drug development. Furthermore,it looks forward to the future directions of development in multi-target combination therapies,aiming to provide theoretical evidence and strategic support for the precise prevention and management of RIOM.

Key words: radiation-induced oral mucositis, small-molecule targeted drugs, oxidative stress, inflammatory response, clinical trials

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