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. 2018 Feb 15;9(3):274. doi: 10.1038/s41419-018-0325-3

Fig. 2. M1 increases apoptosis in susceptible bladder cancer cells.

Fig. 2

a Flow cytometry and annexin V staining analyses of UM-UC-3 and EJ cells treated with M1 (MOI = 1 PFU per cell) and mock control agents. b Numbers of apoptotic cells, as determined by flow cytometry at 24, 48, and 72 h post-infection. c Chromatin condensation was demonstrated via Hoechst 33342 staining. T24 and UM-UC-3 cells were treated with M1 (MOI = 10 PFU per cell) for 72 h. Chromatin condensation is indicated by the white arrows. d Caspase-3/7 activity in T24, UM-UC-3, and EJ cells treated with M1 (MOI = 10 PFU per cell) for 48 h. e Western blots was performed to detect caspase-3 protein expression in the indicated cell lines at 0, 12, 24, and 48 h after M1 (MOI = 10) infection. GAPDH glyceraldehyde-3-phosphate dehydrogenase, CTL control; hpi, hours post-infection. **p < 0.01; ***p < 0.001; N.S., not significant