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口腔牙周炎微生物群通过 γδ T 细胞激活促进口腔鳞状细胞癌的发展。

Oral Microbiota from Periodontitis Promote Oral Squamous Cell Carcinoma Development via γδ T Cell Activation.

机构信息

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.

出版信息

mSystems. 2022 Oct 26;7(5):e0046922. doi: 10.1128/msystems.00469-22. Epub 2022 Aug 24.


DOI:10.1128/msystems.00469-22
PMID:36000726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9600543/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/75422b0b4975/msystems.00469-22-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/16279358200a/msystems.00469-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/ad2185c08879/msystems.00469-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/4fc39c75332b/msystems.00469-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/83a05ed3db44/msystems.00469-22-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/0f5c0dd12742/msystems.00469-22-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/b4e89c89afde/msystems.00469-22-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/75422b0b4975/msystems.00469-22-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/16279358200a/msystems.00469-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/ad2185c08879/msystems.00469-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/4fc39c75332b/msystems.00469-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/83a05ed3db44/msystems.00469-22-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/0f5c0dd12742/msystems.00469-22-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/b4e89c89afde/msystems.00469-22-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b773/9600543/75422b0b4975/msystems.00469-22-f007.jpg

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引用本文的文献

[1]
Demystifying the link between periodontitis and oral cancer: a systematic review integrating clinical, pre-clinical, and in vitro data.

Cancer Metastasis Rev. 2025-9-9

[2]
γδ17T Cells Aggravate Carcinogen-Induced Oral Squamous Cell Carcinoma.

J Dent Res. 2025-5

[3]
Oral microbiota shifts following tooth loss affect gut health.

BMC Oral Health. 2025-2-10

[4]
Relationship Between the Salivary Microbiome and Oral Malodor Metabolites in Older Thai Individuals with Periodontitis and the Cytotoxic Effects of Malodor Compounds on Human Oral Squamous Carcinoma (HSC-4) Cells.

Dent J (Basel). 2025-1-16

[5]
Rodent models for oral microbiome research: considerations and challenges- a mini review.

Front Oral Health. 2024-10-1

[6]
Pharmacomicrobiomics in precision cancer therapy: bench to bedside.

Front Immunol. 2024

[7]
Oral microbial dysbiosis in patients with oral cavity cancers.

Clin Oral Investig. 2024-6-17

[8]
Association of Periodontal Red Complex Bacteria With the Incidence of Gastrointestinal Cancers: A Systematic Review and Meta-Analysis.

Cureus. 2024-4-29

[9]
overgrowth disrupts the gut microbiota in mice bearing oral cancer.

Mycology. 2023-10-26

[10]
Heat-killed Prevotella intermedia promotes the progression of oral squamous cell carcinoma by inhibiting the expression of tumor suppressors and affecting the tumor microenvironment.

Exp Hematol Oncol. 2024-3-21

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Lung microbiota: Unexploited treasure hidden in the immune microenvironment of lung cancer.

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