Metformin Inhibits NLRP3 Inflammasome Expression and Regulates Inflammatory Microenvironment to Delay the Progression of Colorectal Cancer.

Gaojie Liu, Feixiang Wang, Yanlin Feng, Hongsheng Tang
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Abstract

Background: Colorectal cancer is a common malignant tumor, with about one million people diagnosed with it worldwide each year. Recent studies have found that metformin can inhibit the production of inflammatory factors and regulate the polarization of immune cells. However, whether metformin can regulate the inflammatory microenvironment and delay the progression of colorectal cancer by inhibiting the inflammatory response has not been deeply studied yet.

Objective: This study aimed to explore the molecular mechanism by which metformin inhibits the expression of NLRP3 inflammasome, regulates the inflammatory microenvironment, and delays the progression of colorectal cancer through in vitro cell experiments.

Methods: In this research, NLRP3 was knocked down in human colorectal cancer cells, and metformin was added to them. Cell proliferation ability was detected by CCK8, and cell migration and invasion abilities were assessed by Transwell assay. The apoptosis rate was determined by flow cytometry. In addition, the expression of NLRP3 inflammatory vesicles and inflammatory factors in each group of cells was studied by qRT-PCR and Western blotting. Finally, clinical colorectal cancer samples were analyzed by immunohistochemistry.

Results: The results of the study showed that NLRP3 expression was significantly increased in colorectal cancer cell lines and human colorectal cancer tissues. Knockdown of NLRP3 significantly inhibited tumor cell proliferation, migration, and invasion. In addition, the proliferation, migration and invasion of tumor cells were also significantly reduced by the addition of metformin intervention. Furthermore, qRT-PCR and WB results demonstrated that the expression of IL-1β, IL-6, TNF- α, TGF-β, and IL-10 was down-regulated in LS1034 tumor cells after NLRP3 knockdown. In addition, metformin intervention also resulted in different degrees of downregulation of NLRP3 and inflammatory factor expression (p <0.05). Notably, the reduction in inflammatory factors was more pronounced after the combination of NLRP3 knockdown and metformin intervention.

Conclusion: Metformin can inhibit the expression of NLRP3 inflammasome, thereby suppressing the expression of inflammation-related factors, reducing the damage of the inflammatory microenvironment to normal cells, and delaying the progression of colorectal cancer.

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二甲双胍抑制 NLRP3 炎症小体的表达并调节炎症微环境,从而延缓结直肠癌的进展。
背景:结直肠癌是一种常见的恶性肿瘤,全世界每年约有 100 万人被确诊为结直肠癌。最近的研究发现,二甲双胍可以抑制炎症因子的产生,并调节免疫细胞的极化。然而,二甲双胍是否能通过抑制炎症反应来调节炎症微环境并延缓结直肠癌的进展尚未得到深入研究:本研究旨在通过体外细胞实验,探讨二甲双胍抑制NLRP3炎性体表达、调节炎性微环境、延缓结直肠癌进展的分子机制:方法:本研究在人大肠癌细胞中敲除 NLRP3,并加入二甲双胍。用 CCK8 检测细胞增殖能力,用 Transwell 试验评估细胞迁移和侵袭能力。细胞凋亡率由流式细胞术测定。此外,还通过 qRT-PCR 和 Western 印迹法研究了各组细胞中 NLRP3 炎性小泡和炎性因子的表达。最后,对临床结直肠癌样本进行了免疫组化分析:研究结果表明,NLRP3 在结直肠癌细胞系和人类结直肠癌组织中的表达明显增加。敲除 NLRP3 能明显抑制肿瘤细胞的增殖、迁移和侵袭。此外,加入二甲双胍干预后,肿瘤细胞的增殖、迁移和侵袭也明显减少。此外,qRT-PCR和WB结果显示,NLRP3敲除后,LS1034肿瘤细胞中IL-1β、IL-6、TNF- α、TGF-β和IL-10的表达下调。此外,二甲双胍干预也会导致不同程度的 NLRP3 和炎症因子表达下调(p 结论:二甲双胍可抑制 NLRP3 和炎症因子的表达:二甲双胍可抑制 NLRP3 炎性体的表达,从而抑制炎症相关因子的表达,减轻炎性微环境对正常细胞的损伤,延缓结直肠癌的进展。
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