Figure 4. Targeting GLUT1, either in vitro or in vivo, effectively inhibits tumor initiation by CSCs.
(A) Mice (3 for each group) were implanted subcutaneously with the indicated numbers of viable PANC-1 CSLCs that had been treated without (Control) or with 10 μM WZB117 for 6 days. (B) Mice implanted subcutaneously with the indicated numbers of viable PANC-1 CSLCs (3 for each group) were administered a daily intraperitoneal injection of the control vehicle or WZB117 (20 mg/kg/day) for 10 consecutive days starting on the next day of implantation.(C) Mice (4 for each group) were implanted subcutaneously with PANC-1 CSLCs. After 30 days, when the tumor volumes ranged from 292 to 1080 mm3, the mice were randomized and received a daily intraperitoneal injection of the control vehicle or WZB117 (20 mg/kg/day) for 10 consecutive days. In (A) through (C), tumor volume was measured at the indicated time points after implantation, and the results are presented in the graphs as means + SD of each group. *p<0.05 (WZB117 5 × 105 compared against Control 5 × 105 in (A) and (B)).