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张璐, 刘铄川, 王琦珂, 姬高, 武艺铭, 杨利梅, 隋华, 刘怀民. 阿克曼菌对AOM/DSS炎症相关性结直肠癌发生的作用[J]. 肿瘤防治研究, 2023, 50(4): 351-356. DOI: 10.3971/j.issn.1000-8578.2023.22.1200
引用本文: 张璐, 刘铄川, 王琦珂, 姬高, 武艺铭, 杨利梅, 隋华, 刘怀民. 阿克曼菌对AOM/DSS炎症相关性结直肠癌发生的作用[J]. 肿瘤防治研究, 2023, 50(4): 351-356. DOI: 10.3971/j.issn.1000-8578.2023.22.1200
ZHANG Lu, LIU Shuochuan, WANG Qike, JI Gao, WU Yiming, YANG Limei, SUI Hua, LIU Huaimin. Effects of Akkermansia on AOM/DSS Inflammatory-associated Colorectal Cancer[J]. Cancer Research on Prevention and Treatment, 2023, 50(4): 351-356. DOI: 10.3971/j.issn.1000-8578.2023.22.1200
Citation: ZHANG Lu, LIU Shuochuan, WANG Qike, JI Gao, WU Yiming, YANG Limei, SUI Hua, LIU Huaimin. Effects of Akkermansia on AOM/DSS Inflammatory-associated Colorectal Cancer[J]. Cancer Research on Prevention and Treatment, 2023, 50(4): 351-356. DOI: 10.3971/j.issn.1000-8578.2023.22.1200

阿克曼菌对AOM/DSS炎症相关性结直肠癌发生的作用

Effects of Akkermansia on AOM/DSS Inflammatory-associated Colorectal Cancer

  • 摘要:
    目的 探讨阿克曼菌(AKK)对氧化偶氮甲烷(AOM)/葡聚糖硫酸钠(DSS)诱导的炎症相关性结直肠癌小鼠模型及其肠道干细胞的影响。
    方法 AOM/DSS诱导小鼠炎症相关性结直肠癌模型随机分为三组,通过灌胃方式给予三组不同的药物分别为模型组(Model)、AKK组及阿司匹林组(Aspirin)。干预10周后观察小鼠的肿瘤数目、肿瘤大小、肿瘤分布及分析肿瘤负荷情况。免疫组织化学分析表征肿瘤恶性化的蛋白Ki67和表征干细胞的特异性蛋白Lgr5的表达变化。qRT-PCR检测干细胞分化特性的基因Lgr5、CD133、Nanog和ALDH1的mRNA表达。
    结果 与模型组相比,AKK组的肿瘤数目、肿瘤大小及肿瘤负荷明显减小(P < 0.01);相较于模型组小鼠,AKK组的肿瘤组织中Ki67和Lgr5表达明显下降(P < 0.05);CD133、Nanog和ALDH1的mRNA表达明显下调。
    结论 AKK对AOM/DSS诱导的结肠炎相关性结直肠癌小鼠具有防治作用,其作用机制可能与结直肠干细胞活性密切相关。

     

    Abstract:
    Objective To investigate the effects of Akkermansia muciniphila (AKK) on azomethane-oxide (AOM)/glucan sodium sulfate (DSS)-induced inflammatory colorectal cancer mouse model and intestinal stem cells.
    Methods AOM/DSS-induced mouse models of inflammatory-associated colorectal cancer were randomly divided into three groups, namely, model, AKK and aspirin groups, based on different administration of drugs by gavage. The tumor number, size, distribution, and burden were observed 10 weeks after intervention. Immunohistochemical method was used to analyze the expressions of Ki67 and Lgr5 proteins, which are utilized to characterize tumor malignancy and stem cells. The mRNA expressions of Lgr5, CD133, Nanog, and ALDH1 were detected by qRT-PCR.
    Results Compared with those of the model group, the tumor number, size, and burden of the AKK group were significantly reduced (P < 0.01). The expressions of Ki67 and Lgr5 in the AKK group of tumor tissues were significantly decreased (P < 0.05), and the mRNA expressions of CD133, Nanog and ALDH1 were significantly down-regulated.
    Conclusion AKK is effective against AOM/DSS-induced colitis-associated colorectal cancer in mice, and its mechanism of action may be closely related to colorectal stem cell activity.

     

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