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Figure 1: The effect of FL34 on the apoptosis of glioblastoma cells. (a) FL34 treatment-induced apoptosis of U-87 MG cells. Cells were incubated with FL34 for 72 h, stained with annexin-V-FITC/PI, and analyzed by flow cytometry. The flow cytometry results are shown as quantitative bar graphs in which the error bars indicate standard deviation. *P < 0.05, **P < 0.01 versus control cells (ai), Representative scatter diagram of apoptosis after annexin-V-FITC/PI double staining analyzed by flow cytometry (aii); (b) FL34 treatment-induced apoptosis of T98G cells. Cells were incubated with FL34 for 72 h, stained with annexin V-FITC/PI, and analyzed by flow cytometry. The flow cytometry results are shown as quantitative bar graphs, in which the error bars indicate standard deviation. *P < 0.05, **P < 0.01, ***P < 0.001 versus control cells (bi); Representative scatter diagram of apoptosis after annexin-V-FITC/PI double staining analyzed by flow cytometry (bii)

Figure 1: The effect of FL34 on the apoptosis of glioblastoma cells. (a) FL34 treatment-induced apoptosis of U-87 MG cells. Cells were incubated with FL34 for 72 h, stained with annexin-V-FITC/PI, and analyzed by flow cytometry. The flow cytometry results are shown as quantitative bar graphs in which the error bars indicate standard deviation. *<i>P</i> < 0.05, **<i>P</i> < 0.01 versus control cells (ai), Representative scatter diagram of apoptosis after annexin-V-FITC/PI double staining analyzed by flow cytometry (aii); (b) FL34 treatment-induced apoptosis of T98G cells. Cells were incubated with FL34 for 72 h, stained with annexin V-FITC/PI, and analyzed by flow cytometry. The flow cytometry results are shown as quantitative bar graphs, in which the error bars indicate standard deviation. *<i>P</i> < 0.05, **<i>P</i> < 0.01, ***<i>P</i> < 0.001 versus control cells (bi); Representative scatter diagram of apoptosis after annexin-V-FITC/PI double staining analyzed by flow cytometry (bii)