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Ceramide in apoptotic signaling and anticancer therapy

Journal

CURRENT MEDICINAL CHEMISTRY
Volume 13, Issue 14, Pages 1609-1616

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/092986706777441986

Keywords

ceramide; sphingolipid; apoptosis; protein kinase; protein phosphatase; mitochondria; caspase; anticancer

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Ceramide, a product of sphingolipid metabolism, is generated in response to various stress stimuli, such as tumor necrosis factor-alpha, CD95/Fas, chemotherapeutic agents, and irradiation. Ceramide may modulate the biochemical and cellular processes that lead to apoptosis. However, the mechanisms by which ceramide regulates apoptotic events are not fully defined. It is believed that the biological effect of ceramide depends on its concentration, the activation or differentiation status of the cell, and the time frame of action. Here, we discuss the metabolism and cell apoptotic signaling of ceramide. The involvement of protein kinases (i.e. PI3K/Akt and GSK-3 beta) and protein phosphatases (i.e. PP1 and PP2A), Bcl-2 family proteins, mitochondrial damage, and caspase cascade activation are demonstrated. Further, ceramide and its derivatives have recently been incorporated into strategies for anticancer therapies. An understanding of the apoptotic signaling pathways mediated by ceramide may shed light on its potential for therapeutic intervention.

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