Liu Tai-Guo, Huang Ying, Cui Dan-Dan, Huang Xiao-Bing, Mao Shu-Hua, Ji Ling-Ling, Song Hai-Bo, Yi Cheng
Division of Abdominal Cancer, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, PR China.
BMC Cancer. 2009 Jul 23;9:250. doi: 10.1186/1471-2407-9-250.
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.
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.
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.
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.
人参皂苷Rg3是从人参中提取的一种皂苷,可抑制血管生成。低剂量化疗与抗血管生成抑制剂联合使用比传统疗法或单独使用抗血管生成药物更有效地抑制实验性肿瘤的生长。本研究旨在评估低剂量吉西他滨联合人参皂苷Rg3对小鼠已建立的Lewis肺癌血管生成和生长的疗效。
将接种Lewis肺癌的C57L/6小鼠随机分为对照组、人参皂苷Rg3组、吉西他滨组和联合治疗组。记录小鼠的生活质量和生存期。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坏死情况、血流信号以及肿瘤动脉血流的动态参数,如收缩期峰值流速(PSV)和阻力指数(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)。
人参皂苷Rg3组和联合治疗组小鼠的生活质量优于对照组和吉西他滨组。人参皂苷Rg3与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疗效,还显著提高了肿瘤坏死率。此外,联合治疗可明显降低肿瘤中VEGF表达、MVD以及血流信号和PSV。
人参皂苷Rg3联合吉西他滨可能显著抑制肺癌的血管生成和生长,并改善荷瘤小鼠的生存期和生活质量。化疗与抗血管生成药物联合可能是人类肺癌实验治疗中一种创新且有前景的治疗策略。