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首页> 外文期刊>Gastroenterology Report >Antitumor immunity of low-dose cyclophosphamide: changes in T cells and cytokines TGF-beta and IL-10 in mice with colon-cancer liver metastasis
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Antitumor immunity of low-dose cyclophosphamide: changes in T cells and cytokines TGF-beta and IL-10 in mice with colon-cancer liver metastasis

机译:低剂量环磷酰胺的抗肿瘤免疫:与结肠癌肝转移的小鼠中T细胞和细胞因子TGF-β和IL-10的变化

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BackgroundThe tumor immune microenvironment is one of the most important prognostic factors in liver metastasis from colorectal cancer. Low-dose cyclophosphamide (CTX) is widely believed to be involved in the modulation of the immune system. However, the underlying mechanism of low-dose CTX remains unknown. This study aimed to investigate the antitumor immunity of low-dose CTX in the treatment of colon-cancer liver metastasis.MethodsThirty mice were randomly divided into five groups. After liver metastasis was established in colon-cancer models, mice in the treatment groups were injected with low-dose CTX (20?mg/kg) at different time points. Liver and spleen tissues were examined for T-cell markers via flow cytometry. Interleukin (IL)-10 and transforming growth factor (TGF)-β1 expression levels in liver tissues were analysed by immunohistochemistry. Serum interferon (IFN)-γ and IL-10 levels were detected by enzyme-linked immunosorbent assay. An additional 20 mice were randomly allocated into two groups and the survival times were recorded.ResultsThe expression levels of CD4+ T cells, CD8+ T cells, and IFN-γ were down-regulated, whereas those of IL-10 and TGF-β1 were up-regulated in liver metastasis from colon cancer in mice. Furthermore, the local and systemic microenvironments of the liver were altered, which led to reduced antitumor immune responses and subsequently liver metastasis. However, treatment with low-dose CTX reversed these effects. The survival times of mice treated with low-dose CTX were significantly longer than those of the other groups.ConclusionsLow-dose CTX exerts its antitumor activity by changing the systemic and local immune microenvironments and enhancing immune regulation in mice. CTX could be used as a drug to prevent and treat liver metastasis from colon cancer.
机译:背景技术肿瘤免疫微环境是从结肠直肠癌中肝转移中最重要的预后因素之一。低剂量环磷酰胺(CTX)被广泛认为参与免疫系统的调节。然而,低剂量CTX的潜在机制仍然未知。本研究旨在研究低剂量CTX治疗结肠癌肝脏转移的抗肿瘤免疫。方法随机分为五组。在结肠癌模型中建立肝转移后,在不同时间点的低剂量CTX(20×Mg / kg)注射治疗组中的小鼠。通过流式细胞术检查肝脏和脾组织的T细胞标记物。通过免疫组织化学分析肝组织中白细胞介素(IL)-10和转化生长因子(TGF)-β1表达水平。通过酶联免疫吸附试验检测血清干扰素(IFN)-γ和IL-10水平。将另外的20只小鼠随机分配到两组中,并记录存活时间。将CD4 + T细胞,CD8 + T细胞和IFN-γ的表达水平进行下调,而IL-10和TGF-β1的表达水平为上升 - 从小鼠中的结肠癌中解释肝脏转移。此外,肝脏的局部和全身微环境改变,其导致抗肿瘤免疫应答和随后的肝转移。然而,用低剂量CTX治疗逆转了这些效果。用低剂量CTX处理的​​小鼠的存活时间明显高于其他基团的小鼠。结合,通过改变全身和局部免疫微环境并提高小鼠免疫调节来施加其抗肿瘤活性。 CTX可用作预防和治疗来自结肠癌的肝转移的药物。

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