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. 2018 Nov 13;7:e38865. doi: 10.7554/eLife.38865

Figure 1. GL261-DTR model allows manageable tumor growth.

(A) Survival curve of mice injected with GL261-DTR cells and the response to DT or combined DT and fWBI treatments. DT treatment was given at 1 ug daily between Day 7 and 12, the combined DT and fWBI treatment group received extra DT treatment at 1 ug every other day between Day 31 and 45. **ptumor + DT = 0.0076, **ptumor + DT + fWBI=0.0033, Mantel-Cox Log-rank test compared to the tumor only group. (B) BLI of the tumor only and the tumor +DT groups. DT treatment resulted in delayed tumor growth. (C) BLI of mice received combined DT and fWBI treatment. Irradiation further delayed tumor growth, and extra DT treatment was able to delay growth of tumors when they recur. (tumor only no treatment control, DT and DT +fWBI treatments were randomly allocated among tumor bearing mice, N = 5 – 7 each treatment group, median survival is labeled next to the curve of each group, sample size was selected to minimize the number of animals used for this pilot experiment.

Figure 1—source data 1. source data are included in Figure 1—source data 1).
DOI: 10.7554/eLife.38865.004

Figure 1.

Figure 1—figure supplement 1. Response of GL261-DTR cells to 48 hr’ DT treatment in vitro.

Figure 1—figure supplement 1.

Treatment with 10 ng/ml DT killed all GL261-DTR cells in 48 hr.