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Exercise effects on polyp burden and immune markers in the ApcMin/+ mouse model of intestinal tumorigenesis

机译:运动对ApcMin / +小鼠肠癌发生模型中息肉负担和免疫标记的影响

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摘要

Many observational epidemiologic studies suggest an association between exercise and colon cancer risk. The mechanisms contributing to a preventative effect of exercise on colon cancer are complex and multifaceted. Altered immune system function is one possible mechanism that has been largely unexplored. Therefore, the purpose of this study was to examine the effects of exercise on markers associated with macrophages and select T cell populations in a mouse model of intestinal tumorigenesis and to relate this to polyp characteristics. Male ApcMin/+ mice were randomly assigned to either sedentary (Sed) or exercise (Ex) treatment (n=6–9/group). The exercise treatment consisted of treadmill running for 1 h/day and 6 days a week at 15 m/min from 4 until 16 weeks of age. Intestinal polyps were counted and categorized by size. Mucosal tissue was analyzed for mRNA expression of overall macrophages (F4/80), for genes associated with M1 (IL-12, IL-23 and Nos2) and M2 (CD206, IL-10, IL-4, CCL17, CCL22 and Arg-1) macrophages and the macrophage chemoattractants MCP-1, fetuin A and CXCL14. Markers for cytotoxic T cells (CTLs) and regulatory T cells were also examined by measuring mRNA expression of CD8 and Foxp3, respectively. While there was no significant difference in overall polyp number between the groups (Sed, 23.3±4.3; and Ex, 16.5±4.3), Ex did have a reduction in the number of large polyps (Sed, 6.1±1.1; and Ex, 3.0±0.6) (P<0.05). This was consistent with a decrease in spleen weight (P<0.05). Similarly, Ex reduced mRNA expression of overall macrophages (F4/80) as well as markers associated with both M1 (IL-12) and M2 (CD206, CCL22 and Arg-1) subtypes (P<0.05) but there was no significant decrease in macrophage chemoattractants. CD8 expression was increased while Foxp3 expression was decreased with Ex (P<0.05). Overall the data provide important new information on immune regulation as a possible mechanism for the documented benefits of exercise training on reducing colon cancer progression.
机译:许多观察性流行病学研究表明,运动与结肠癌风险之间存在关联。预防锻炼对结肠癌的作用的机制是复杂且多方面的。免疫系统功能改变是一种可能的机制,目前尚未得到充分探索。因此,本研究的目的是检查运动对与巨噬细胞相关的标志物的影响,并在肠肿瘤发生小鼠模型中选择T细胞群,并将其与息肉特征相关联。将雄性Apc Min / + 小鼠随机分配至久坐(Sed)或运动(Ex)治疗(n = 6–9 /组)。运动治疗包括在4至16周龄时以15 m / min的速度每周跑步1 h和每天6天的跑步机。计数肠息肉并按大小分类。分析了粘膜组织的整体巨噬细胞(F4 / 80),与M1(IL-12,IL-23和Nos2)和M2(CD206,IL-10,IL-4,CCL17,CCL22和Arg相关的基因的mRNA表达-1)巨噬细胞和巨噬细胞趋化因子MCP-1,胎球蛋白A和CXCL14。还分别通过测量CD8和Foxp3的mRNA表达来检查细胞毒性T细胞(CTL)和调节性T细胞的标记。虽然两组之间的总息肉数目没有显着差异(Sed,23.3±4.3; Ex,16.5±4.3),但Ex的大息肉数目却减少了(Sed,6.1±1.1; Ex,3.0 ±0.6)(P <0.05)。这与脾脏重量的减少是一致的(P <0.05)。同样,Ex降低了整体巨噬细胞(F4 / 80)的mRNA表达以及与M1(IL-12)和M2(CD206,CCL22和Arg-1)亚型相关的标志物(P <0.05),但没有明显降低在巨噬细胞趋化因子中。随着Ex的增加,CD8表达增加而Foxp3表达减少(P <0.05)。总体而言,数据提供了有关免疫调节的重要新信息,这是运动训练对减少结肠癌进展的益处的文献报道的可能机制。

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