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©2011 Baishideng Publishing Group Co.
World J Gastroenterol. Aug 21, 2011; 17(31): 3605-3613
Published online Aug 21, 2011. doi: 10.3748/wjg.v17.i31.3605
Published online Aug 21, 2011. doi: 10.3748/wjg.v17.i31.3605
Figure 1 Ginsenoside Rg3 inhibits cell viability of human and murine liver cancer cells.
A: Concentration-dependent inhibitory effects of Ginsenoside Rg3 on cell viability in Hep1-6 and HepG2 cell lines. Cells were treated with Rg3 at 0, 50, 100, 200 μg/mL in 10% fetal bovine serum-supplemented medium for 24 h; cell viability was determined by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay (n = 6 for Hep1-6, n = 6 for HepG2). B: Time-dependent inhibitory effects of Rg3 on cell viability in Hep1-6 and HepG2 cell lines. Cells were treated with Rg3 100 μg/mL for 0, 6, 12, 24, 48 h. One-way ANOVA was performed to test the concentration and time-dependent effects. aP < 0.05 vs untreated controls.
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Citation: Jiang JW, Chen XM, Chen XH, Zheng SS. Ginsenoside Rg3 inhibit hepatocellular carcinoma growth
via intrinsic apoptotic pathway. World J Gastroenterol 2011; 17(31): 3605-3613 - URL: https://www.wjgnet.com/1007-9327/full/v17/i31/3605.htm
- DOI: https://dx.doi.org/10.3748/wjg.v17.i31.3605