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首页> 外文期刊>BMC Cancer >Inhibitory effect of ginsenoside Rg3 combined with gemcitabine on angiogenesis and growth of lung cancer in mice
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Inhibitory effect of ginsenoside Rg3 combined with gemcitabine on angiogenesis and growth of lung cancer in mice

机译:人参皂苷Rg3联合吉西他滨对小鼠血管生成和肺癌生长的抑制作用

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Background Ginsenoside Rg3, a saponin extracted from ginseng, inhibits angiogenesis. The combination of low-dose chemotherapy and anti-angiogenic inhibitors suppresses growth of experimental tumors more effectively than conventional therapy or anti-angiogenic agent alone. The present study was designed to evaluate the efficacy of low-dose gemcitabine combined with ginsenoside Rg3 on angiogenesis and growth of established Lewis lung carcinoma in mice. Methods C57L/6 mice implanted with Lewis lung carcinoma were randomized into the control, ginsenoside Rg3, gemcitabine and combination group. The quality of life and survival of mice were recorded. Tumor volume, inhibitive rate and necrosis rate were estimated. Necrosis of tumor and signals of blood flow as well as dynamic parameters of arterial blood flow in tumors such as peak systolic velocity (PSV) and resistive index (RI) were detected by color Doppler ultrasound. In addition, expression of vascular endothelial cell growth factor (VEGF) and CD31 were observed by immunohistochemstry, and microvessel density (MVD) of the tumor tissues was assessed by CD31 immunohistochemical analysis. Results Quality of life of mice in the ginsenoside Rg3 and combination group were better than in the control and gemcitabine group. Combined therapy with ginsenoside Rg3 and gemcitabine not only enhanced efficacy on suppression of tumor growth and prolongation of the survival, but also increased necrosis rate of tumor significantly. In addition, the combination treatment could obviously decrease VEGF expression and MVD as well as signals of blood flow and PSV in tumors. Conclusion Ginsenoside Rg3 combined with gemcitabine may significantly inhibit angiogenesis and growth of lung cancer and improve survival and quality of life of tumor-bearing mice. The combination of chemotherapy and anti-angiogenic drugs may be an innovative and promising therapeutic strategy in the experimental treatment of human lung cancer.
机译:背景人参皂苷Rg3(一种从人参中提取的皂苷)可抑制血管生成。低剂量化学疗法和抗血管生成抑制剂的组合比单独使用常规疗法或抗血管生成剂更有效地抑制了实验性肿瘤的生长。本研究旨在评估低剂量吉西他滨联合人参皂苷Rg3对已建立的Lewis肺癌小鼠血管生成和生长的功效。方法将植入Lewis肺癌的C57L / 6小鼠随机分为对照组,人参皂苷Rg3,吉西他滨和联合治疗组。记录小鼠的生活质量和存活率。估计肿瘤体积,抑制率和坏死率。通过彩色多普勒超声检测肿瘤的坏死和血流信号,以及动脉中动脉血流的动态参数,例如峰值收缩速度(PSV)和电阻指数(RI)。此外,通过免疫组织化学观察血管内皮细胞生长因子(VEGF)和CD31的表达,并通过CD31免疫组织化学分析评估肿瘤组织的微血管密度(MVD)。结果人参皂苷Rg3组和联合组小鼠的生活质量均优于对照组和吉西他滨组。人参皂苷Rg3和吉西他滨联合治疗不仅增强了抑制肿瘤生长和延长生存期的功效,而且显着提高了肿瘤的坏死率。另外,联合治疗可明显降低肿瘤中的VEGF表达和MVD以及血流和PSV信号。结论人参皂苷Rg3联合吉西他滨可显着抑制肺癌的血管生成和生长,改善荷瘤小鼠的生存和生活质量。化学疗法和抗血管生成药物的组合在人类肺癌的实验治疗中可能是一种创新且有希望的治疗策略。

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