Ligature-Induced Periodontitis Drives Colorectal Cancer: An Experimental Model in Mice

牙周炎 结直肠癌 医学 结扎 癌症 牙科 内科学
作者
Y T Shi,Jiamin He,Zian Tong,Yuanyi Qian,Qingfeng Wang,Dingjiacheng Jia,Wenyue Zhu,Yibing Zhao,Botao Cai,S.J. Chen,Misi Si
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:102 (6): 689-698 被引量:21
标识
DOI:10.1177/00220345231158269
摘要

Periodontitis is a prevalent inflammatory oral disease associated with an increased risk of colorectal cancer. Experimental animal models are critical tools to investigate the effects and mechanisms of periodontitis on colorectal cancer. Several murine periodontitis models have been used in research, including oral gavage, periodontal pathogen injection, and ligature models. The role of experimental periodontitis caused by silk ligation in colorectal cancer remains unclear. In this study, we used an experimental periodontitis model on a colitis-associated colorectal cancer model and a spontaneous model, respectively. We observed the promotion of colorectal cancer in ligature-induced periodontitis mice compared to those control mice in 2 different models, as assessed by tumor number, tumor size, and tumor load. Since bacterial dysbiosis is an important feature of periodontitis, we next analyzed the oral and gut microbiomes using 16S ribosomal RNA gene sequencing. We found that the experimental periodontitis model reshaped the microbial community in the oral cavity and gut. In addition, we found a higher extent of programmed death 1 (PD-1)–positive CD8 + T-cell infiltration in tumor samples of the periodontitis group than in controls by immunofluorescence staining. Regarding the potential molecular mechanism, we transplanted the fecal microbiota of the periodontitis patient into mice and observed a tumor-promoting effect in the periodontitis group, assessed by tumor volume and tumor weight, together with a low level of INF-γ + CD8 + T-cell infiltration in subcutaneous tumor mice. Taken together, we show that ligature-induced periodontitis model promotes colorectal cancer by microbiota remodeling and suppression of the immune response.
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