AI Article Synopsis

  • Sphingosine 1-phosphate (S1P) is a key bioactive lipid involved in important cellular processes such as proliferation, survival, and migration, with its levels being crucial for normal bodily functions.
  • Sphingosine phosphate lyase (SPL) plays a critical role in regulating S1P by degrading it, thus affecting the balance of S1P in the body, which has implications for various diseases.
  • Current research indicates that targeting SPL could offer new therapeutic options for treating conditions like cancer, autoimmune disorders, and inflammation.

Article Abstract

Background: Sphingosine 1-phosphate (S1P) is a bioactive lipid that regulates cell proliferation, survival and migration and plays an essential role in angiogenesis and lymphocyte trafficking. S1P levels in the circulation and tissues are tightly regulated for proper cell functioning, and dysregulation of this system may contribute to the pathophysiology of certain human diseases. Sphingosine phosphate lyase (SPL) irreversibly degrades S1P and thereby acts as a gatekeeper that regulates S1P signaling by modulating intracellular S1P levels and the chemical S1P gradient that exists between lymphoid organs and circulating blood and lymph. However, SPL also generates biochemical products that may be relevant in human disease. SPL has been directly implicated in various physiological and pathological processes, including cell stress responses, cancer, immunity, hematopoietic function, muscle homeostasis, inflammation and development.

Objective/methods: This review summarizes the current know-ledge of SPL structure, function and regulation, its involvement in various disease states and currently available small molecules known to modulate SPL activity.

Results/conclusion: This review provides evidence that SPL is a potential target for pharmacological manipulation for the treatment of malignant, autoimmune, inflammatory and other diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774446PMC
http://dx.doi.org/10.1517/14728220903039722DOI Listing

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