Original Articles
Copyright ©2009 The WJG Press and Baishideng.
World J Gastroenterol. Apr 21, 2009; 15(15): 1816-1820
Published online Apr 21, 2009. doi: 10.3748/wjg.15.1816
Figure 1
Figure 1 Effect of acetylshikonin on proliferation of SGC-7901 cells in vitro. SGC-7901 cells were treated with various concentrations of acetylshikonin for 48 h. Tumor growth inhibitory rate was determined by MTT assay.
Figure 2
Figure 2 Effect of acetylshikonin on expression of Bcl-2 and Bax in SGC-7901 cells. Lower panel: Ratios of protein quantitation of Bcl-2 or Bax to actin. Each experiment was independently performed three times. aP < 0.05, bP < 0.01 vs control group.
Figure 3
Figure 3 Effect of acetylshikonin on Bcl-2 and Bax mRNA expression levels in SGC-7901 cells. Lower panel: Ratios of mRNA quantitation of Bcl-2 or Bax to actin. Each experiment was independently performed three times. aP < 0.05, bP < 0.01 vs control group.
Figure 4
Figure 4 Anti-tumor effects of acetylshikonin in vivo. Representative tumors from each group were shown. Lower panel: Average tumor weight of sacrificed animals. aP < 0.05, bP < 0.01 vs control group.
Figure 5
Figure 5 Effect of acetylshikonin on expression of Bax, Bcl-2 and Caspase 3 in SGC-7901 tumor tissues. Tumor tissue sections showed strong Bax/Caspase 3 cytoplasmic staining and weak Bcl-2 cytoplasmic staining of tumor cells in acetylshikon treatment groups, as well as the integrated optical density (IOD) for the expression of Bax, Bcl-2 and Caspase 3 in SGC-7901 cells. aP < 0.05, bP < 0.01 vs control group.