CP-31398 restores mutant p53 tumor suppressor function and inhibits UVB-induced skin carcinogenesis in mice
J. Clin. Invest. Xiuwei Tang, et al. 117:3753 doi:10.1172/JCI32481 [
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Figure 6Effects of CP-31398 treatment on the induction of apoptosis in neonatal human epidermal keratinocytes and human epidermoid carcinoma A431 cells. (
A) Western blot showing the expression of apoptosis proteins. (
B) Western blot showing the expression of cell-cycle regulatory proteins in A431 cells following CP-31398 treatment. (
C) Effect of CP-31398 on the induction of apoptosis and release of mitochondrial proteins in NHEKs carrying wild-type p53 and A431 cells carrying mutant p53. (
D) Effect of CP-31398 on the changes in mitochondrial membrane potential in A431 cells. A431 cells were treated with PBS (control) or various concentrations of CP-31398 as indicated in the figure for different time intervals. For Western blot analysis, 100 μg protein was loaded in each well. Each experiment was repeated at least 3 times. For assaying mitochondrial membrane potential, A431 cells were treated with PBS (control) or 10, 20, and 40 μg/ml of CP-31398 for 10 minutes and stained with JC-1 dye. Carbonyl cyanide 3-chlorophenylhydrazone (CCCP) was used as positive control. Error bars represent mean ± SD of triplicate samples.