Figure 4
Figure 4. The antitumor effect of CpG-Stat3 siRNA is immune mediated but does not depend on activation of host’s APCs. (A-B) NOD/SCID/IL-2RγKO or (C-D) Tlr9−/− mice (n = 6) were challenged intravenously with 1 × 106 CMM+ AML cells and treated by using CpG-Stat3 siRNA or CpG-Luc siRNA or left untreated as in Figure 2. (A,C) Stat3 gene silencing was confirmed by qPCR; (B,D) percentages of GFP+c-Kit+ AML cells in different organs were determined by flow cytometry. Shown are means ± SEM from two independent experiments. Statistically significant differences were indicated by asterisks: ***P < .001; **P < .01; *P < .05.

The antitumor effect of CpG-Stat3 siRNA is immune mediated but does not depend on activation of host’s APCs. (A-B) NOD/SCID/IL-2RγKO or (C-D) Tlr9−/− mice (n = 6) were challenged intravenously with 1 × 106CMM+ AML cells and treated by using CpG-Stat3 siRNA or CpG-Luc siRNA or left untreated as in Figure 2. (A,C) Stat3 gene silencing was confirmed by qPCR; (B,D) percentages of GFP+c-Kit+ AML cells in different organs were determined by flow cytometry. Shown are means ± SEM from two independent experiments. Statistically significant differences were indicated by asterisks: ***P < .001; **P < .01; *P < .05.

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