4.7 Article

Therapeutic Strategies and Pharmacological Tools Influencing S1P Signaling and Metabolism

期刊

MEDICINAL RESEARCH REVIEWS
卷 37, 期 1, 页码 3-51

出版社

WILEY
DOI: 10.1002/med.21402

关键词

sphingosine kinase; sphingosine; S1P; ceramide; S1P lyase; S1P receptor; fingolimod; antibodies; clinical candidates

资金

  1. EU COST actions [CA15135, CM1207]
  2. DFG [INST208/664-1FUGG]
  3. LOEWE program Fh-TMP
  4. LOEWE program OSF
  5. LOEWE program NEFF
  6. Else-Kroner-Fresenius-Stiftung (EKFS)
  7. Deutsches Konsortium fur Translationale Krebsforschung (DKTK)

向作者/读者索取更多资源

During the last two decades the study of the sphingolipid anabolic, catabolic, and signaling pathways has attracted enormous interest. Especially the introduction of fingolimod into market as first p.o. therapeutic for the treatment of multiple sclerosis has boosted this effect. Although the complex regulation of sphingosine-1-phosphate (S1P) and other catabolic and anabolic sphingosine-related compounds is not fully understood, the influence on different (patho)physiological states from inflammation to cytotoxicity as well as the availability of versatile pharmacological tools that represent new approaches to study these states are described. Here, we have summarized various aspects concerning the many faces of sphingolipid function modulation by different pharmacological tools up to clinical candidates. Due to the immense heterogeneity of physiological or pharmacological actions and complex cross regulations, it is difficult to predict their role in upcoming therapeutic approaches. Currently, inflammatory, immunological, and/or antitumor aspects are discussed. (C) 2016 Wiley Periodicals, Inc.

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