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. 2020 Apr 1;43(4):384–396. doi: 10.14348/molcells.2020.2230

Fig. 9. Enhanced cell death in BCSCs treated with shRNA-C under oxidative stress conditions.

Fig. 9

(A) Transfection efficiency images of shRNA-C expressing a lentiviral vector for the knock-down of the CD66c gene. (B) Cell viability of BCSCs treated with shRNA-C under oxidative stress conditions. Data are expressed as the mean ± SEM. **P < 0.02 for in the absence or presence of H2O2. ***P < 0.01 for H2O2-only group versus H2O2treated with shRNA-C group. (C) FACS analysis of cell death induced by treatment with H2O2 post-shRNA-C transfection in BCSCs. (D) Quantitative viable cell population of BCSCs treated with shRNA-C and H2O2 by FACS analysis. Data are expressed as the mean ± SEM. *P < 0.05 or **P < 0.02 for the comparison of no H2O2 treated groups and H2O2 treated groups or **P < 0.02 for shRNA-SC versus shRNA-C groups in the presence of H2O2. ***P < 0.01 for the comparison of NC and shRNA-C groups in the presence of H2O2. (E) Quantitative death cell population induced by shRNA-C treatment with H2O2. Data are expressed as the mean ± SEM. *P < 0.05 or **P < 0.02 for in the absence or presence of H2O2. **P < 0.02 for the comparison of shRNA-SC with H2O2 group and shRNA-C with H2O2 group. ***P < 0.01 for the comparison of H2O2 only group and shRNA-C with H2O2 group.