Figure 3.
Figure 3. Cytoplasmic nucleoside kinase activity is elevated in AML. (A) Relative quantification of total intracellular ddC and ddCTP by LC-MS/MS in primary human AML (samples B1-B6) and normal hematopoietic progenitor samples following treatment with 2 µM ddC for 6 days. ddC and ddCTP content were normalized to total protein input and represented as mean ± SD (n = 2) of technical replicates within each independent experiment. Levels of ddC and ddCTP in each panel represent semiquantitative values. Each panel represents a separate experiment. Differences between ddC or ddCTP levels in each AML sample compared with mean of normal samples within an experiment was assessed using the Bonferroni posttest after 1-way ANOVA or the Student t test. *P < .05, ***P < .001. (B) Correlation between levels of ddC and ddCTP from samples in panel A was determined using the Pearson correlation method. BLQ, below the limit of quantification.

Cytoplasmic nucleoside kinase activity is elevated in AML. (A) Relative quantification of total intracellular ddC and ddCTP by LC-MS/MS in primary human AML (samples B1-B6) and normal hematopoietic progenitor samples following treatment with 2 µM ddC for 6 days. ddC and ddCTP content were normalized to total protein input and represented as mean ± SD (n = 2) of technical replicates within each independent experiment. Levels of ddC and ddCTP in each panel represent semiquantitative values. Each panel represents a separate experiment. Differences between ddC or ddCTP levels in each AML sample compared with mean of normal samples within an experiment was assessed using the Bonferroni posttest after 1-way ANOVA or the Student t test. *P < .05, ***P < .001. (B) Correlation between levels of ddC and ddCTP from samples in panel A was determined using the Pearson correlation method. BLQ, below the limit of quantification.

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