bongkrekic-acid and Skin-Neoplasms

The tumor suppressor p53 can translocate into mitochondria and activate apoptosis. Here we studied whether p53 mitochondrial translocation and subsequent apoptosis were affected by blocking mitochondrial permeability transition pore using cyclosporine A (CsA) and bongkrekic acid (BA) in skin epidermal JB6 cells and skin tissues. Our results demonstrated that CsA and BA blocked TPA-induced p53 translocation, leading to protection against the loss of mitochondrial membrane potential and Complex I activity, and eventually suppression of apoptosis. Thus, our results suggest that mitochondrial permeability transition is required for p53 mitochondrial translocation.

Topics: Animals; Bongkrekic Acid; Cell Line; Cyclosporine; Membrane Potentials; Mice; Mice, Inbred DBA; Mitochondria; Protein Transport; Skin Neoplasms; Tetradecanoylphorbol Acetate; Tumor Suppressor Protein p53