Study on anti-tumor activities of ginsenoside structure modification HRG in vivo
- Author:
Feng-Li ZHAO
1
Author Information
1. Department of Pharmacology
- Publication Type:Journal Article
- Keywords:
Angiogenesis;
Chick chorioallantoic membrane;
Ginsenoside structure modification 3β,12β,20(S)-trihydroxy dammarane-3-O-β-D-glucopyranosyl(1-2)-β-D-glucopyranoside, HRG;
Implanted tumor;
Liver cancer H22 cell
- From:
Chinese Pharmaceutical Journal
2012;47(20):1625-1629
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE: To explore the anti-tumor activities of a new compound 3β,12β,20(S)-trihydroxy dammarane-3-O-β-D-glucopyranosyl (1-2)-β-D-glucopyranoside (HRG), which is a substance of ginsenoside structure modification, in vivo. METHODS: Liver cancer H22 tumor model on the chick chorioallantoic membrane (CAM) was established to observe the effects of HRG on tumor growth, the number of induced vessels and the growth inhibition rate. The implanted tumors were dyed by hematoxylin-eosin (HE), and the morphological properties were studied with light microscope. Immunohistochemistry (SP method) was used to detect the expressions of the implanted tumor's MVD and VEGF. RESULTS: HRG inhibited the tumor growth at 25, 50 and 100 μg · mL-1. Compared with the model control group, the inhibitory rates of the tumor growth were 27.73%, 50.02%, and 64.21%, respectively. HRG significantly reduced the number of tumor-induced vessels. At the same time, there existed different degree necrosis among the treatment groups, and the degree of necrosis had an inverse relationship with the number of tumor-induced vessels. In addition, HRG reduced the MVD of the implanted tumors, and decreased the expression of VEGF. CONCLUSION: HRG has good anti-tumor activities in vivo, and can significantly inhibit the growth of liver cancer H22-CAM tumor and the induction of angiogenesis. The mechanisms may be associated with lower tumor MVD and VEGF expression.
