DocumentCode
3439765
Title
Comparison of effects on the anti-metastasis between isoliquiritigenin and glabridin
Author
Wang Caixia ; Zheng Qiusheng ; Wang Yishan ; Chen Xiaoyu
Author_Institution
Ocean Sch., Yantai Univ., Yantai, China
fYear
2011
fDate
19-22 Aug. 2011
Firstpage
1104
Lastpage
1107
Abstract
The aim of this study was to evaluate the anti-metastasis effects and the inhibition of the tube-like structure formation of human umbilical vein endothelial cells ECV304 of isoliquiritigenin and glabridin. The cell survival ratio of mice melanoma cells B16F1 was measured by SRB assay, the lethality rate was tested by trypan blue exclusion test. The survival ratio of human umbilical vein endothelial cells ECV304 were measured by SRB and AO/EB assays. The migration of B16F1 cells and ECV304 cells were measured by scratch wound assay. The matrix metalloproteinase-2 (MMP-2) activity in B16F1 cells culture medium was measured by gelatin zymography and ELISA methods. The inhibition on tube-like structure formation of human umbilical vein endothelial cells ECV304 were detected on artificial basilar membrane rebuilt by matrigel. Taken together, our data suggested that isoliquiritigenin and glabridin have strong anti-metastasis activities, in the same concentration, isoliquiritigenin has stronger function.
Keywords
biochemistry; biomedical materials; biomembranes; cancer; cell motility; drugs; enzymes; gels; molecular biophysics; patient treatment; ECV304; ELISA methods; antimetastasis; artificial basilar membrane; gelatin zymography; glabridin; human umbilical vein endothelial cells; isoliquiritigenin; lethality rate; matrigel; matrix metalloproteinase-2; mice melanoma cells B16F1; scratch wound assay; tube-like structure formation; Drugs; Humans; Malignant tumors; Metastasis; Wounds; Anti-metastasis; B16F1 cells; ECV304 cells; Glabridin; Isoliquiritigenin;
fLanguage
English
Publisher
ieee
Conference_Titel
Human Health and Biomedical Engineering (HHBE), 2011 International Conference on
Conference_Location
Jilin
Print_ISBN
978-1-61284-723-8
Type
conf
DOI
10.1109/HHBE.2011.6029017
Filename
6029017
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