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. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: SLAS Discov. 2018 May 10;23(7):732–741. doi: 10.1177/2472555218774248

Figure 4.

Figure 4.

Response of T-ALL primary samples (n = 2) and patient derived xenografts (n = 5) to small molecule inhibitors (n = 31). (A) The heatmap represents the mean EC50 values obtained for the samples treated with the drugs for 48 hr under normoxic conditions. The columns indicate T-ALL samples and the rows indicate the tested drugs. The darkest red indicates the most sensitivity (lowest EC50 values) of the tested samples to the tested inhibitors. EC50 values are only reported for compounds that yielded a maximum response values of 20% or greater. For those samples which yielded maximal responses < 20% and/or had EC50 values greater than 100 µM, we report those EC50 values as “100 µM” (light grey). (B) The maximum responses of each T-ALL sample to the tested inhibitors at the highest tested dose, 100 µM, with exception of *alvocidib, *bortezomib and *carfilzomib, for which the highest tested dose was 1 µM. The heatmap indicates the levels of percentage of dead cells, where darkest red indicates 100% propidium iodide positive cells. (C) Representative high throughput dose response curves of T-ALL samples (primary samples, 12–089 and 15–093; patient derived xenografts, PATRAP, PATZZM) treated with the tested inhibitors. The cells were treated in dose responses (afatinib and sunitinib, 0.005 – 100 µM; carfilzomib, 0.05 – 1000 nM) for 48 hr, followed by cell viability analyses by flow cytometry using propidium iodide.