Ceramidase
Ceramidase is an enzyme which cleaves fatty acids from ceramide, producing sphingosine which in turn is phosphorylated by a sphingosine kinase to form sphingosine-1-phosphate.
Function
Ceramide, SPH, and S1P are bioactive lipids that mediate cell proliferation, differentiation, apoptosis, adhesion, and migration. Presently, 7 human ceramidases encoded by 7 distinct genes have been cloned:- acid ceramidase – cell survival
- neutral ceramidase – protective against inflammatory cytokines
- alkaline ceramidase 1 – mediating cell differentiation by controlling the generation of SPH and S1P
- alkaline ceramidase 2 – important for cell proliferation and survival
- alkaline ceramidase 3
Clinical significance
Human neutral ceramidase is an enzyme that plays a critical role in colon cancer and there are currently no potent or clinically effective inhibitors for nCDase reported to date. Inhibitors of nCDase were identified via a high-throughput screening effort of large chemical libraries at Scripps Research. Multiple rounds of chemical optimization ensued with improved potency in terms of IC50 and selectivity over counterscreen assays. The crystal structure of nCDase has been solved and these leads are now being pursued in crystal docking studies and in vitro drug metabolism and pharmacokinetics.