Effect of Liuweidihuang pill and Jinkuishenqi pill on inhibition of spontaneous breast carcinoma growth in mice

被引:11
作者
Zheng Lixiang [1 ]
Liu Hongning [1 ]
Gong Van [1 ]
Meng Xianming [1 ]
Jiang Runde [1 ]
Wang Xiaomin [1 ]
Wang Qiaofeng [1 ]
Wang Yue [1 ]
机构
[1] Jiangxi Univ Tradit Chinese Med, Sch Basic Med, Nanchang 330004, Peoples R China
关键词
Breast neoplasms; Pathology; Vascular endothelial growth factors; Extracellular signal-regulated MAP kinases; Cyclin D1; Liuweidihuang pill; Jinkuishenqi pill; CANCER;
D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
100218 [急诊医学];
摘要
OBJECTIVE: To investigate the preventing and treating action of Liuweidihuang pill (LP) and Jinkuishenqi pill (JP) on spontaneous breast carcinoma in mice. METHODS: A model of spontaneous breast carcinoma was derived from 11.5-month-old female Kunming breeding mice following the delivery of several litters. The mice were randomly divided into five groups: model control group (C), Liuweidihuang pill high-dose group (LH; 4.6 g . kg (- 1) . d (- 1)), Liuweidihuang pill low-dose group (LL; 2.3 g . kg (-1) . d (- 1)), Jinkuishenqi pill high-dose group (JH; 4.6 g . kg (- 1) . d (- 1)) and Jinkuishenqi pill low-dose group (JL; 2.3 g . kg (- 1) . d (- 1)). Cancer tissue volume was measured by water immersion. Histopathology was analyzed by hematoxylin and eosin staining. Vascular endothelial growth factor (VEGF), extracellular signal-regulated kinase (ERK) and cyclin D1 protein expression in cancer tissue was assayed by western blotting. RESULTS: Compared with the control group, cancer tissue volume and weight were lower in the LP and JP groups, and survival time was longer. The expression of VEGF, ERK and Cyclin D1 were inhibited in the LP and JP groups (P < 0.05), and cell differentiation was increased. Tumor weights and volumes and VEGF, ERK and Cyclin D1 expression in LL or LH were significantly lower than in JL and JH (P < 0.01). CONCLUSION: Both LP and JP could restrain cancer growth and promote cancer cell differentiation; moreover, LP was more effective than JP The likely mechanism of action was via inhibition of VEGF, ERK and cyclin D1. (C) 2015 JTCM. All rights reserved.
引用
收藏
页码:453 / 459
页数:7
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