DocumentCode :
2093315
Title :
Trierpenic acids isolated from Betula birch inhibits angiogenesis in vitro and in vivo
Author :
Tao, Ming ; Zheng, Chunwei ; Xin, Nian ; Bian, Xuewen ; Lee, Yan
Author_Institution :
Beijing Inst. of Technol., Beijing
fYear :
2007
fDate :
23-27 May 2007
Firstpage :
1987
Lastpage :
1991
Abstract :
Some trierpenic acids as a effective part for anti-tumor were extracted from Betula birch, HPLC and UV analysis methods were used to optimize extraction artwork and control the total trierpenic acids in the extraction for quantity control especially; In this study, we investigate the inhibitory effects of Trierpenic acids isolated from Betula birch TABB on angiogenesis. The in vitro anti-angiogenic effect of Trierpenic acids isolated from Betula was tested on models of angiogenesis : proliferation , migration of human umbilical vascular endothelial (ECV304) cell; The anti-angiogenic effect in vivo was detected in morphological development on model of chick chorioallantoic membrane. Cox-2mRNA expression was detected by RT-PCR. We found TABB inhibited the growth of human umbilical vascular endothelial (ECV304) cell line in a concentration-dependent manner (1-100 mug/ml).The migration of ECV304 was obviously inhibited by TABB. In CAM assay, TABB could significant inhibited the angiogenesis at the administered dosages (10-30 mug/CAM). And significantly inhibit cox-2 mRNA expression. TABB was shown to inhibit angiogenesis in vitro and in vivo, which may be the mechanism of the treatment of anti-tumor effect.
Keywords :
DNA; cellular biophysics; drugs; inhibitors; tumours; Betula birch; Cox-2mRNA expression; HPLC analysis; UV analysis; angiogenesis inhibition; antitumor; chick chorioallantoic membrane; human umbilical vascular endothelial cell; trierpenic acids; Biochemistry; CADCAM; Cancer; Computer aided manufacturing; Humans; In vitro; In vivo; Isolation technology; Neoplasms; Optimization methods;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
Conference_Location :
Beijing
Print_ISBN :
978-1-4244-1077-4
Electronic_ISBN :
978-1-4244-1078-1
Type :
conf
DOI :
10.1109/ICCME.2007.4382096
Filename :
4382096
Link To Document :
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