口腔医学 ›› 2026, Vol. 46 ›› Issue (10): 763-770.doi: 10.13591/j.cnki.kqyx.2026.10.007

• 基础与临床研究 • 上一篇    下一篇

重度牙周炎患者lncRNA表达谱分析及其调控机制

朱文伟1, 李宏卫2, 王颖3, 李万林3, 郑梦露3, 王育聪3, 桑磊3()   

  1. 1 苏州卫生职业技术学院附属口腔医院牙体牙髓科, 江苏苏州 (215002)
    2 南京医科大学附属口腔医院口腔颌面外科, 江苏南京 (210029)
    3 苏州卫生职业技术学院附属口腔医院口腔颌面外科, 江苏苏州 (215002)
  • 收稿日期:2025-08-17 出版日期:2026-10-28 发布日期:2026-10-16
  • 通讯作者: 桑 磊 E-mail:sorry_2004@sina.com
  • 基金资助:
    苏州卫生职业技术学院院级课题(SZWZY202103);2021年度苏州市应用基础研究(医疗卫生)科技创新面上项目(SKJY2021033)

Analysis of lncRNA expression profile and its regulatory mechanism in patients with severe periodontitis

ZHU Wenwei1, LI Hongwei2, WANG Ying3, LI Wanlin3, ZHENG Menglu3, WANG Yucong3, SANG Lei3()   

  1. Department of Endodontics, Stomatological Hospital, Affiliated Suzhou Vocational Health College, Suzhou 215002, China
  • Received:2025-08-17 Online:2026-10-28 Published:2026-10-16

摘要:

目的 分析重度牙周炎患者长链非编码RNA(long non-coding RNA,lncRNA)表达谱并探讨其潜在调控机制。方法 收集2024年11月—2024年12月于苏州卫生职业技术学院附属口腔医院口腔颌面外科就诊,因重度牙周炎拔牙(试验组)且需同期拔除埋伏阻生第三磨牙(对照组)5例患者患牙的牙龈组织,进行高通量测序,筛选差异表达的lncRNA和mRNA,并从这些mRNA中进一步筛选lncRNA的靶基因,随后对这些靶基因进行GO和KEGG功能富集分析,探讨这些lncRNA在重度牙周炎中的可能调控机制。结果 高通量测序结果显示,共有1 473个lncRNA和7 222个mRNA存在显著差异表达。GO功能富集分析表明,差异表达lncRNA可能通过调控细胞凋亡、适应性免疫反应和内质网应激等生物学过程参与重度牙周炎病理进程。KEGG功能富集分析结果显示,差异表达lncRNA可能通过白细胞经内皮细胞迁移、Fcγ受体介导的吞噬作用、花生四烯酸代谢、药物代谢-细胞色素P450、癌症转录失调等途径,调控重度牙周炎发生发展。结论 在重度牙周炎患者中差异表达的lncRNA可能通过调控适应性免疫反应、细胞凋亡以及内质网应激等生物学过程参与疾病的发生发展。

关键词: 牙周炎, 高通量测序, lncRNA, 表达谱, 生物信息学分析

Abstract:

Objective To analyze the long non-coding RNA (lncRNA) expression profile in patients with severe periodontitis and explore its potential regulatory mechanisms. Methods Gingiva samples were collected from five patients who underwent tooth extraction due to severe periodontitis (test group) and simultaneous extraction of impacted third molars (control group) at the Department of Oral and Maxillofacial Surgery, Affiliated Stomatological Hospital of Suzhou Vocational Health College, between November 2024 and December 2024. High-throughput sequencing was performed to identify differentially expressed lncRNAs and mRNAs. Target genes of these lncRNAs were further screened within these mRNAs, followed by GO and KEGG functional enrichment analysis to investigate the potential regulatory roles of these lncRNAs in severe periodontitis. Results High-throughput sequencing results revealed 1 473 significantly differentially expressed lncRNAs and 7 222 differentially expressed mRNAs. GO enrichment analysis indicated that the differentially expressed lncRNAs may be involved in the pathological process of severe periodontitis by regulating biological processes such as apoptosis, adaptive immune response and endoplasmic reticulum stress. KEGG pathway analysis showed that these lncRNAs might influence the development and progression of severe periodontitis through pathways including leukocyte transendothelial migration, Fcγ receptor-mediated phagocytosis, arachidonic acid metabolism, drug metabolism-cytochrome P450, and transcriptional misregulation in cancer. Conclusion The differentially expressed lncRNAs in patients with severe periodontitis may contribute to the pathogenesis and progress by regulating molecular mechanisms involved in adaptive immune response, apoptosis, and endoplasmic reticulum stress.

Key words: periodontitis, high-throughput sequencing, lncRNA, expression profile, bioinformatics analysis

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