State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan Universitygrid.13291.38, Chengdu, China.
CAS Key Laboratory of Environmental Biotechnology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China.
mSystems. 2022 Oct 26;7(5):e0046922. doi: 10.1128/msystems.00469-22. Epub 2022 Aug 24.
Oral squamous cell carcinoma (OSCC) is a fatal disease, and periodontitis is associated with OSCC development. However, the pathogenesis in the context of OSCC with periodontitis has not been fully understood. Here, we demonstrated that periodontitis promoted OSCC development, accompanied by alterations in the oral bacterial community and the tumor immune microenvironment. The oral microbiota from periodontitis maintained the dominant position throughout the whole process of OSCC with periodontitis, of which was the most abundant genus. The oral microbiota from periodontitis could activate interleukin-17-positive (IL-17) γδ T cells directly. The activated γδ T cells were necessary for the IL-17/signal transducer and activator of transcription 3 (STAT3) pathway and promoted M2-tumor-associated macrophage (TAM) infiltration in OSCC proliferation. Our data provide insight into the carcinogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis. Thus, oral commensal bacteria and IL-17 γδ T cells might be potential targets for monitoring and treating OSCC. The work reveals the role of the oral microbiota from periodontitis in carcinogenesis. Furthermore, our study provides insight into the pathogenesis of OSCC with periodontitis by outlining the tumor-associated immune response shaped by the oral microbiota from periodontitis, which might identify new research and intervention targets for OSCC with periodontitis.
口腔鳞状细胞癌(OSCC)是一种致命的疾病,牙周炎与 OSCC 的发展有关。然而,牙周炎背景下的 OSCC 发病机制尚未完全阐明。在这里,我们证明了牙周炎促进了 OSCC 的发展,伴随着口腔细菌群落和肿瘤免疫微环境的改变。牙周炎的口腔微生物群在整个牙周炎伴 OSCC 过程中保持主导地位,其中 是最丰富的属。牙周炎的口腔微生物群可以直接激活白细胞介素-17 阳性(IL-17)γδ T 细胞。激活的 γδ T 细胞是 IL-17/信号转导和转录激活因子 3(STAT3)通路所必需的,促进了 M2-肿瘤相关巨噬细胞(TAM)在 OSCC 增殖中的浸润。我们的数据通过描绘由牙周炎的口腔微生物群塑造的肿瘤相关免疫反应,提供了对牙周炎伴 OSCC 致癌作用的深入了解。因此,口腔共生细菌和 IL-17 γδ T 细胞可能是监测和治疗 OSCC 的潜在靶点。这项工作揭示了牙周炎的口腔微生物群在致癌作用中的作用。此外,我们的研究通过描绘由牙周炎的口腔微生物群塑造的肿瘤相关免疫反应,提供了对牙周炎伴 OSCC 发病机制的深入了解,这可能为牙周炎伴 OSCC 确定新的研究和干预靶点。
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