Title :
Anti-Tumor Effect and Its Mechanism of Vaccaria segetalis on Mouse Inoculated H22 Solid Carcinoma
Author :
Gao, Yue-ying ; Qiu, Li-ying ; Kang, Xiao-xing ; Wang, Hua ; Liu, Ling-yan ; Feng, Lei ; Jin, Jian
Author_Institution :
Sch. of Med. & Pharm., Jiangnan Univ., Wuxi, China
Abstract :
AIM Vaccaria segetalis was reported anti-tumor action in vitro. In this study, the effect and mechanism of inhibiting tumor growth and improving the quality of life of Vaccaria segetalis on mouse inoculated H22 solid carcinoma were investigated. METHODS The solid carcinoma model of mouse was made by H22 cells subcutaneous injection and they were divided into four groups including model control group, 1mg/kg treatment dose, 2.5mg/kg treatment dose and 5mg/kg treatment dose groups of Vaccaria segetalis. After ig treatment for 10 days, the mice were killed, and the inhibited rate of tumor growing was calculated. The pathological morphologic change of tumor was observed by HE staining. The apoptosis number of tumor was observed by TUNEL method. The expression of CD31 of tumor endothelial cells was measured by immunohistochemical method. RESULTS Vaccaria segetalis can improve the quality of life on mice invased by tumor, inhibit the growth of tumor. The effect of Vaccaria segetalis on the tumor morphology showed nuclear shrinkage, necrosis, and inflammatory cell infiltration on the periphery, etc. And it inhibited the expression of CD31, induced apoptosis of tumor cells and vascular endothelial cells. CONCLUSION Vaccaria segetalis can improve the the quality of life on mice invased by tumor, and inhibit the growth of tumor. The mechanisms were likely due to inhibiting the angiogenesis, and inducing the apoptosis of tumor cells and vascular endothelial cells.
Keywords :
biochemistry; cellular biophysics; diseases; drugs; molecular biophysics; patient treatment; physiological models; tumours; CD31 expression; H22 cell subcutaneous injection; TUNEL method; Vaccaria segetalis; angiogenesis; antitumor effect; apoptosis; drug treatment; ig treatment; immunohistochemical method; inflammatory cell infiltration; mass 1 mg; mass 2.5 mg; mass 5 mg; mice; mouse inoculated H22 solid carcinoma; necrosis; nuclear shrinkage; pathological morphologic change; solid carcinoma model; time 10 day; treatment dose; tumor endothelial cells; tumor growth inhibition; tumor morphology; vascular endothelial cells; Cancer; Drugs; Helium; Immune system; In vitro; Mice; Neoplasms; Pathology; Solid modeling; Tumors;
Conference_Titel :
Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
Conference_Location :
Chengdu
Print_ISBN :
978-1-4244-4712-1
Electronic_ISBN :
2151-7614
DOI :
10.1109/ICBBE.2010.5517710