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. 2016 Feb 4;7(9):10297–10321. doi: 10.18632/oncotarget.7185

Figure 11. The down-regulation of EGFR enhances sensitivity to anti-cancer drugs.

Figure 11

(A) Malme3MR cells were transiently transfected with the indicated siRNA (each at 10 nM). At 24 h after transfection, cells were then with the indicated anti-cancer drugs for 24 h, followed by MTT assays. (B) Malme3MR cells were transiently transfected with the indicated siRNA (10 nM). At 24 h after transfection, cells were then with taxol (1 μM), gefitinib (1 μM) or trastuzumab (10 μg/ml) for 24 h, followed by caspase-3 activity assays. Ttm denotes trastuzumab. **p < 0.005; ***p < 0.0005. (C) Same as (B) except that immunoblot analysis was performed. (D) Malme3MR cells were transiently transfected with the indicated siRNA (each at 10 nM). At 48 h after transfection, cell lysates were subjected to immunoblot analysis (left panel). Malme3MR cells were transiently transfected with the indicated siRNA (10 nM) along with the indicated construct (1 μg). At 48 h after transfection, immunoblot analysis was performed (right panel). (E) Malme3MR cells were transiently transfected with the indicated siRNA (10 nM) along with the indicated construct (1 μg). At 24 h after transfection, cells were then treated with taxol (1 μM), gefitinib (1 μM) or trastuzumab (10 μg/ml) for 24 h, followed by caspase-3 activity assays. **p < 0.005.