References
- Billich, A., Bornancin, F., Devay, P., Mechtcheriakova, D., Urtz, N. andBaumruker, T. (2003) Phosphorylation of the immunomodulatorydrug FTY720 by sphingosine kinases. J. Biol. Chem. 278, 47408-47415. https://doi.org/10.1074/jbc.M307687200
- Brinkmann, V. (2009) FTY720 (fingolimod) in Multiple Sclerosis: therapeuticeffects in the immune and the central nervous system. Br. J.Pharmacol. 158, 1173-1182. https://doi.org/10.1111/j.1476-5381.2009.00451.x
- Claus, R., Russwurm, S., Meisner, M., Kinscherf, R. and Deigner, H. P.(2000) Modulation of the ceramide level, a novel therapeutic concept?Curr. Drug Targets 1, 185-205. https://doi.org/10.2174/1389450003349272
- Hannun, Y. A. and Obeid, L. M. (1995) Ceramide: an intracellular signalfor apoptosis. Trends Biochem. Sci. 20, 73-77. https://doi.org/10.1016/S0968-0004(00)88961-6
- Hengst, J. A., Wang, X., Sk, U. H., Sharma, A. K., Amin, S. and Yun,J. K. (2010) Development of a sphingosine kinase 1 specific small-moleculeinhibitor. Bioorg. Med. Chem. Lett. 20, 7498-74502. https://doi.org/10.1016/j.bmcl.2010.10.005
- Hla, T., Lee, M. J., Ancellin, N., Paik, J. H. and Kluk, M. J. (2001) Lysophospholipids-receptor revelations. Science 294, 1875-1878. https://doi.org/10.1126/science.1065323
- Igarashi, Y., Hakomori, S., Toyokuni, T., Dean, B., Fujita, S., Sugimoto,M., Ogawa, T., Ghendy, K. and Racker, E. (1989) Effect of chemicallywell-defined sphingosine and its N-methyl derivatives onprotein kinase C and src kinase activities. Biochemistry 28, 6796-6800. https://doi.org/10.1021/bi00443a002
- Johnson, K. R., Becker, K. P., Facchinetti, M. M., Hannun, Y. A. andObeid, L. M. (2002) PKC-dependent activation of sphingosine kinase1 and translocation to the plasma membrane. J. Biol. Chem.38, 35257-35262.
- King, C. C., Zenke, F. T., Dawson, P. E., Dutil, E. M., Newton, A. C.,Hemmings, B. A., and Bokoch, G. M. (2000) Sphingosine is a novelactivator of 3-phosphoinositide-dependent kinase 1. J. Biol. Chem.275, 18108-18113. https://doi.org/10.1074/jbc.M909663199
- Kluk, M. J. and Hla, T. (2002) Signaling of sphingosine-1-phosphatevia the SIP/EDG-family of G-protein-coupled receptors. Biochim.Biophys. Acta. 1582, 72-80. https://doi.org/10.1016/S1388-1981(02)00139-7
- Kwon, Y. B., Kim, C. D., Youm, J. K., Gwak, H. S., Park, B. D., Lee, S.H., Jeon S., Kim, B. J., Seo, Y. J., Park, J. K. and Lee, J. H. (2007)Novel synthetic ceramide derivatives increase intracellular calciumlevels and promote epidermal keratinocyte differentiation. J. LipidRes. 48,1936-1943 https://doi.org/10.1194/jlr.M700185-JLR200
- Lee, M. J., Van Brocklyn, J. R., Thangada, S., Liu, C. H., Hand, A. R.,Menzeleev, R., Spiegel, S. and Hla, T. (1996) Sphingosine 1-phosphateas a ligand for the G-protein-coupled receptor EDG-1. Science279, 1552-1555.
- Maceyka, M., Payne, S.G., Milstien, S. and Spiegel, S. (2002) Sphingosinekinase, sphingosine-1-phosphate, and apoptosis. Biochim.Biophys. Acta. 1585, 193-201. https://doi.org/10.1016/S1388-1981(02)00341-4
- McDonald, O. B., Hannun, Y. A., Reynolds, C. H. and Sahyoun, N.(1991) Activation of casein kinase II by sphingosine. J. Biol. Chem.266, 21773-21776.
- Megidish, T., White, T., Takio, K., Titani, K., Igarashi, Y. and Hakomori,S. (1995) The signal modulator protein 14-3-3 is a target ofsphingosine- or N,N-dimethylsphingosine-dependent kinase in 3T3(A31) cells. Biochem. Biophys. Res. Commun. 216, 739-747. https://doi.org/10.1006/bbrc.1995.2684
- Ogretmen, B. and Hannun, Y. A. (2001) Updates on functions of ceramidein chemotherapy-induced cell death and in multidrug resistance.Drug Resist. Updat. 4, 368-377. https://doi.org/10.1054/drup.2001.0225
- Olivera, A., Rosenfeldt, H.M., Bektas, M., Wang, F., Ishii, I., Chun,J., Milstien, S. and Spiegel, S. (2003) Sphingosine kinase type1 induces G12/13-mediated stress fi ber formation, yet promotesgrowth and survival independent of G protein-coupled receptors. J.Biol. Chem. 278, 46452-46460. https://doi.org/10.1074/jbc.M308749200
- Paugh, S. W., Payne, S. G., Barbour, S. E., Milstien, S. and Spiegel,S. (2003) The immunosuppressant FTY720 is phosphorylated bysphingosine kinase type 2. FEBS Lett. 554, 189-193. https://doi.org/10.1016/S0014-5793(03)01168-2
- Pitman, M. R. and Pitson S. M. (2010) Inhibitors of the sphingosinekinase pathway as potential therapeutics. Curr. Cancer Drug Targets10, 354-367. https://doi.org/10.2174/156800910791208599
- Pyne, S. and Pyne, N. J. (2000) Sphingosine 1-phosphate signaling inmammalian cells. Biochem. J. 349, 385-402. https://doi.org/10.1042/0264-6021:3490385
- Pyne, N. J. and Pyne, S. (2008) Sphingosine 1-phosphate, lysophosphatidicacid and growth factor signaling and termination. Biochim.Biophys. Acta. 1781, 467-476. https://doi.org/10.1016/j.bbalip.2008.05.004
- Sharma, A. K., Sk, U. H., Gimbor, M. A., Hengst, J. A., Wang, X., Yun,J. and Amin, S. (2010) Synthesis and bioactivity of sphingosinekinase inhibitors and their novel aspirinyl conjugated analogs. Eur.J. Med. Chem. 45, 4149-4156. https://doi.org/10.1016/j.ejmech.2010.06.005
- Spiegel, S., English, D. and Milstien, S. (2002) Sphingosine 1-phosphatesignaling: providing cells with a sense of direction. TrendsCell Biol. 12, 236-242. https://doi.org/10.1016/S0962-8924(02)02277-8
- Walter S., and Fassbender K. (2010) Spingolipids in Multiple Sclerosis.Cell Physiol. Biochem. 26, 49-56. https://doi.org/10.1159/000315105
- Watterson, K., Sankala, H., Milstien, S. and Spiegel, S. (2003) Pleiotropicactions of sphingosine-1-phosphate. Prog. Lipid Res. 42,344-357. https://doi.org/10.1016/S0163-7827(03)00015-8
- Xia, P., Wang, L., Gamble J.R. and Vadas, M.A. (1999) Activation ofsphingosine kinase by tumor necrosis factor-alpha inhibits apoptosisin human endothelial cells. J. Biol. Chem. 274, 34499-34505. https://doi.org/10.1074/jbc.274.48.34499
- Xia, P., Gamble, J. R., Wang, L., Pitson, S. M., Moretti, P. A., Wattenberg,B. W., D’Andrea, R. J. and Vadas, M. A. (2000) An oncogenicrole of sphingosine kinase. Curr. Biol. 10, 1527-1530. https://doi.org/10.1016/S0960-9822(00)00834-4