Figure 5.
Figure 5. Effects of imatinib and/or As4S4 on BCR-ABL oncoprotein and PTK activity in K562 cells and primary CML cells. (A) Western blot analysis of BCR-ABL of K562 cells after 48 hours of treatment. (B) PTK activity of K562 cells and primary BMMNCs from CML-AP patients. Analysis was performed after treatment with As4S4 and/or imatinib for 24 hours and 48 hours (n = 3, mean ± SD). Statistical analysis using a one-side paired t test (*, P < .05 versus control; ▴, P < .01 versus control; ☆, P < .05 versus imatinib, As4S4 group, and control; ⋆, P < .01 versus imatinib, As4S4 group, and control; #, P < .05 versus imatinib, As4S4 group, and P < .01 versus control). CON indicates control; I 0.2, 0.2 μM imatinib; I 0.25, 0.25 μM imatinib; A2, 2 μM As4S4; A2.5, 2.5 μM As4S4; I 0.2A2, 0.2 μM imatinib and 2 μM As4S4; and I 0.25A2.5, 0.25 μM imatinib and 2.5 μM As4S4.

Effects of imatinib and/or As4S4 on BCR-ABL oncoprotein and PTK activity in K562 cells and primary CML cells. (A) Western blot analysis of BCR-ABL of K562 cells after 48 hours of treatment. (B) PTK activity of K562 cells and primary BMMNCs from CML-AP patients. Analysis was performed after treatment with As4S4 and/or imatinib for 24 hours and 48 hours (n = 3, mean ± SD). Statistical analysis using a one-side paired t test (*, P < .05 versus control; ▴, P < .01 versus control; ☆, P < .05 versus imatinib, As4S4 group, and control; ⋆, P < .01 versus imatinib, As4S4 group, and control; #, P < .05 versus imatinib, As4S4 group, and P < .01 versus control). CON indicates control; I 0.2, 0.2 μM imatinib; I 0.25, 0.25 μM imatinib; A2, 2 μM As4S4; A2.5, 2.5 μM As4S4; I 0.2A2, 0.2 μM imatinib and 2 μM As4S4; and I 0.25A2.5, 0.25 μM imatinib and 2.5 μM As4S4.

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