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Fig.1 | Cell & Bioscience

Fig.1

From: β-adrenergic receptor inhibition enhances oncolytic herpes virus propagation through STAT3 activation in gastric cancer

Fig.1

Efficacy of cell killing by oncolytic T1012G and propranolol as separate agents and combined treatment on cell proliferation in gastric cancer cell lines. A and B CCK8 assay measured cell viability after T1012G (0.01, 0.05, 0.1, 1, 2,5 MOI) and propranolol (20, 40, 60, 80, 100,120,160 µM) treatment for 48 h. C and E The survival rate from the co-treatment of T1012G (0.01, 0.05, 0.1, 1, 2, 5 MOI) and propranolol (40, 60 µM in HGC and AGS; 60, 80 µM in MFC) at 48 h. F HGC-27 cells were seeded on 96-well plates. After 48 h of incubation with or without propranolol (40 μmol/l), cells were infected with different dose of virus (0.01, 0.05, 0.1, 0.5, 1 MOI). The number of surviving cells in each well was determined 2 days after infection. Data are presented as mean ± SEM. Significant differences were evaluated using one-way ANOVA, and the asterisk (*) indicates a significant difference compared the same T1012G dose or propranolol alone with the combination group using Games-Howell's multiple comparisons test (P < 0.05). Pro, propranolol. 40/60/80 µM → indicates the cell viability corresponding to propranolol treatment alone

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