Papuamine causes autophagy following the reduction of cell survival through mitochondrial damage and JNK activation in MCF-7 human breast cancer cells

• Published in: International journal of oncology Vol. 43; no. 5; pp. 1413 - 1419
• Main Authors: Kanno, Syu-Ichi, Yomogida, Shin, Tomizawa, Ayako, Yamazaki, Hiroyuki, Ukai, Kazuyo, Mangindaan, Remy E P, Namikoshi, Michio, Ishikawa, Masaaki
• Format: Journal Article
• Language: English
• Published: Greece Spandidos Publications UK Ltd 01.11.2013; D.A. Spandidos
• Subjects: Alkaloids - pharmacology; Apoptosis; Apoptosis - drug effects; Autophagy; Blotting, Western; Breast cancer; Breast Neoplasms - drug therapy; Breast Neoplasms - enzymology; Breast Neoplasms - pathology; Cancer therapies; Cell Proliferation; Cell Survival - drug effects; Cytochrome; Cytochromes c - metabolism; Cytotoxicity; Female; Humans; Kinases; MAP Kinase Kinase 4 - metabolism; Membrane Potential, Mitochondrial - drug effects; Mitochondria; Mitochondria - drug effects; Mitochondria - enzymology; Mitochondria - pathology; Proteins; Proto-Oncogene Proteins c-bcl-2 - metabolism; Signal transduction; Tumor Cells, Cultured; United States > US; Japan
• ISSN: 1019-6439; 1791-2423
• DOI: 10.3892/ijo.2013.2093

We previously reported that extracts of an Indonesian marine sponge Haliclona sp. showed potent cytotoxicity and the induction of apoptosis against human solid cancer cell lines. In this study, we examine the cytotoxic mechanism of the major chemical compound, papuamine, on MCF-7 human breast cancer cells. Papuamine at 5 µM did not show significant cytotoxic effects after incubation for 24 h, but autophagosome vesicular formation was apparent. At 10 µM of papuamine, significant reduction in cell survival was observed at 12 h, and increases in autophagy at this concentration were time-dependent and apparent before the appearance of cytotoxic effects. Both the release of cytochrome c to the cytosol and increase in Bax in the mitochondrial fraction were found to be concentration-dependent. Moreover, mitochondrial membrane potential shows concentration- and time-dependent decreases with exposure to papuamine. The release of cytochrome c has been shown to be accompanied by an increase in JNK activation. 3-Methyladenine (MA), a classical autophagy inhibitor showed increased JNK activation by exposure to papuamine. In conclusion, our results indicate that papuamine causes earlier onset autophagy and delayed reduction of cell survival through mitochondrial damage and JNK activation in MCF-7 cells.