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Biochem Res Int. 2012; 2012: 248135.
Published online 2012 February 9. doi:  10.1155/2012/248135
PMCID: PMC3286894
Sphingolipid and Ceramide Homeostasis: Potential Therapeutic Targets
Simon A. Young, 1 John G. Mina, 2 Paul W. Denny, 2, 3 * and Terry K. Smith 1 *
1School of Biology and Chemistry, Biomedical Sciences Research Complex, University of St Andrews, North Haugh, KY16 9ST, UK
2Biophysical Sciences Institute, School of Biological and Biomedical Sciences and Department of Chemistry, University of Durham University Science Laboratories, South Road, Durham DH1 3LE, UK
3School of Medicine and Health, Durham University, Queen's Campus, Stockton-on-Tees TS17 6BH, UK
*Paul W. Denny: p.w.denny/at/durham.ac.uk and
*Terry K. Smith: tks1/at/st-andrews.ac.uk
Academic Editor: Todd B. Reynolds
Received July 31, 2011; Accepted October 20, 2011.
Abstract
Sphingolipids are ubiquitous in eukaryotic cells where they have been attributed a plethora of functions from the formation of structural domains to polarized cellular trafficking and signal transduction. Recent research has identified and characterised many of the key enzymes involved in sphingolipid metabolism and this has led to a heightened interest in the possibility of targeting these processes for therapies against cancers, Alzheimer's disease, and numerous important human pathogens. In this paper we outline the major pathways in eukaryotic sphingolipid metabolism and discuss these in relation to disease and therapy for both chronic and infectious conditions.
Articles from Biochemistry Research International are provided here courtesy of
Hindawi Publishing Corporation