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Ceramide signaling in apoptosis

Adriana Haimovitz‐FriedmanDepartment of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, USARichard KolesnickDepartment of Radiation Oncology and Laboratory of Signal Transduction, Memorial Sloan-Kettering Cancer CenterNew York, USAZvi FuksDepartment of Radiation Oncology and Laboratory of Signal Transduction, Memorial Sloan-Kettering Cancer CenterNew York, USA
1997en
ABI

Аннотация

The sphingomyelin pathway is a ubiquitous, evolutionarily conserved signaling system initiated by hydrolysis of the plasma membrane phospholipid sphingomyelin to generate ceramide. Ceramide acts as a second messenger in activating the apoptotic cascade. Diverse cytokine receptors and environmental stresses utilize ceramide to signal apoptosis. In several cell systems ceramide links to the stress-activated protein kinase (SAPK)/c-jun kinase (JNK) cascade to signal apoptosis. The engagement of the sphingomyelin pathway in signaling apoptosis is tightly regulated by anti-apoptotic control mechanisms, and the balance between pro- and anti-apoptotic systems determines the magnitude of the apoptotic response in vitro and in vivo. This review describes the known elements and molecular ordering of ceramide-mediated apoptosis and the anti-apoptotic mechanisms that regulate its expression. Understanding of pro- and anti-apoptotic signaling involved in ceramide-mediated apoptosis and the modes of their co-ordinated function may yield opportunities for pharmacological interventions with potential for clinical applications.

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