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Yifei Tongluo, a Chinese Herbal Formula, Suppresses Tumor Growth and Metastasis and Exerts Immunomodulatory Effect in Lewis Lung Carcinoma Mice

机译:中国草药配方,益绒通罗抑制肿瘤生长和转移,并在刘易斯肺癌小鼠中施加免疫调节作用

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摘要

This study was aimed to investigate the anti-tumor, anti-metastasis and immunomodulatory effects of Yifei Tongluo (YFTL), a Chinese herbal formula, in Lewis lung carcinoma mice and to explore the underlying mechanisms. LLC cells were inoculated subcutaneously in C57BL/6 mice to establish the Lewis lung carcinoma model. We observed that YFTL effectively inhibited tumor growth and prolonged the overall survival of tumor-bearing mice. Additionally, YFTL treatment resulted in a significantly decreased number of surface lung metastatic lesions compared with the model control group. Meanwhile, TUNEL staining confirmed that the tumors from YFTL-treated mice exhibited a markedly higher apoptotic index. The results suggest that Akt and mitogen-activated protein kinase (MAPKs) pathways may be involved in YFTL-induced apoptosis. The results show that YFTL also inhibited the vascular endothelial growth factor (VEGF), matrix metalloproteinases (MMP)-2, MMP-9, N-cadherin, and Vimentin expression, but increased E-cadherin expression. Mechanistic studies indicated that YFTL could suppress the angiogenesis and the epithelial-mesenchymal transition (EMT) of the tumor through Akt/ERK1/2 and TGF1/Smad2 pathways. In addition, YFTL also showed immunomodulatory activities in improving the immunosuppressive state of tumor-bearing mice. Therefore, our findings could support the development of YFTL as a potential antineoplastic agent and a potentially useful anti-metastatic agent for lung carcinoma therapy.
机译:本研究旨在探讨刘易斯肺癌小鼠中艾菲通络(YFT1),刘易斯肺癌小鼠的抗肿瘤,抗转移和免疫调节效果,探索潜在机制。将LLC细胞皮下皮下接种在C57BL / 6小鼠中以建立Lewis肺癌模型。我们观察到yftl有效地抑制肿瘤生长并延长了肿瘤小鼠的整体存活。另外,与模型对照组相比,YFT1处理导致表面肺转移性病变数显着降低。同时,TUNEL染色证实,来自YFFL处理的小鼠的肿瘤表现出明显更高的凋亡指数。结果表明,AKT和丝裂剂激活的蛋白激酶(MAPK)途径可参与YFFL诱导的细胞凋亡。结果表明,YFF1还抑制了血管内皮生长因子(VEGF),基质金属蛋白酶(MMP)-2,MMP-9,N-CDERHERIN和VIMENTIN表达,而是增加了E-Cadherin表达。机械研究表明,YFT1可以通过AKT / ERK1 / 2和TGF1 / SMAD2途径抑制肿瘤的血管生成和上皮 - 间充质转变(EMT)。此外,YFF1还显示出免疫调节活性,改善携带肿瘤小鼠的免疫抑制状态。因此,我们的研究结果可以支持YFTL作为潜在的抗肿瘤剂和肺癌治疗的潜在抗转移剂的发展。

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  • 来源
    《Molecules》 |2019年第4期|共17页
  • 作者单位

    Shandong Univ Sch Pharmaceut Sci 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

    Shandong Univ Sch Pharmaceut Sci 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

    Shandong Univ Sch Pharmaceut Sci 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

    Shandong Univ Sch Pharmaceut Sci 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

    Shandong Univ Sch Basic Med Sci Dept Pathol &

    Pathophysiol 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

    Shandong Univ Sch Pharmaceut Sci 44 West Wenhua Rd Jinan 250012 Shandong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

    lung cancer; antitumor; anti-metastasis; apoptosis; MMPs; immunomodulatory; MAPK pathway;

    机译:肺癌;抗肿瘤;抗转移;细胞凋亡;MMPS;免疫调节;MAPK途径;

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