Ursolic acid induces apoptosis through mitochondrial intrinsic pathway and caspase-3 activation in M4Beu melanoma cells

• DOI: 10.1002/ijc.20588
• Publication Date: 2004-11-02T20:22:20Z
• Authors: Pierre-Olivier Ha...; Rapha�l Duval; Christiane Delage; Alain Simon
• Keywords: Skin Neoplasms; Antineoplastic Agents; Apoptosis; 03 medical and health sciences; [SDV.SP.MED]Life Sciences [q-bio]/Pharmaceutical sciences/Medication; Cell Line, Tumor; Humans; Melanoma; Cell Proliferation; bcl-2-Associated X Protein; 0303 health sciences; Flavoproteins; Caspase 3; Reverse Transcriptase Polymerase Chain Reaction; Cell Cycle; Apoptosis Inducing Factor; Membrane Proteins; Cholic Acids; [SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology; Mitochondria; 3. Good health; Enzyme Activation; Gene Expression Regulation, Neoplastic; Proto-Oncogene Proteins c-bcl-2; Caspases; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology

Over the coming years, skin cancer could become a significant public health problem. Previous results indicate that ursolic acid (UA), a pentacyclic triterpene acid, has pleiotropic biologic activities such as antiinflammatory and antiproliferative activities on cancer cells. As UA represents a promising chemical entity for the protection of human skin, in agreement with tests done by the cosmetic industry, we investigated its effects on the M4Beu human melanoma cell line. In this report, we demonstrated for the first time that UA had a significant antiproliferative effect on M4Beu, associated with the induction of an apoptotic process, characterized by caspase-3 activation, the downstream central effector of apoptosis. We demonstrated that UA-induced apoptosis was dependent on the mitochondrial intrinsic pathway, as shown by transmembrane potential collapse (DeltaPsim) and by alteration of the Bax-Bcl-2 balance, with a concomitant increase in Bax expression and decrease in Bcl-2 expression. We also showed that UA-induced DeltaPsim was associated with apoptosis-inducing factor leakage from mitochondria. Taken together, our results suggest that UA-induced apoptosis on M4Beu cells is accomplished via triggering of mitochondrial pathway. In conclusion, UA could be an encouraging compound in the treatment or prevention of skin cancer and may represent a new promising anticancer agent in the treatment of melanoma.