Abstract
Human melanoma is the most aggressive form of human skin cancer, and is notoriously resistant to any current modalities of cancer therapy. Here we show that lonidamine (LND), a mitochondria-targeting non-conventional chemotherapeutic agent, markedly induced apoptosis in radioresistant human malignant melanoma C32TG cells. Either LND of up to 250 μM or X-ray irradiation of up to 15 Gy alone induced only a few percent of the apoptosis when administrated separately. When the two agents were combined, the apoptosis prominently increased to 29.3 %. The apoptotic cells thus induced by the combination treatment showed chromatin condensation, a depletion in ΔΨm, and an activation of caspase-3. A pan-caspase inhibitor Z-Asp-CH2DCB completely suppressed the apoptosis. The combination treatment also decreased Bcl-2 and Bad-phosphorylation. These results indicate that the mitochondria pathway of apoptosis would devise a new radiotherapy strategy for treating malignant melanoma.
