| Literature DB >> 32093531 |
Marjorie Argollo1,2, Federica Furfaro2, Daniela Gilardi2, Giulia Roda2, Mariangela Allocca2,3, Laurent Peyrin-Biroulet4, Silvio Danese2,3.
Abstract
Introduction: Sphingosine-1-phosphate (S1P) is a membrane-derived lysophospholipid signaling molecule implicated in various physiological and pathological processes, such as regulation of the immune, cardiovascular, pulmonary, and nervous systems and theoretical cancer-related risks, through extracellular activation of S1P1-5 receptors.Areas covered: S1P receptor agonism is a novel strategy for the treatment of UC targeting lymphocyte recirculation, through blockade of lymphocyte egress from lymph nodes. We conducted an extensive literature review on PUBMED on currently available data on molecular aspects of S1P modulation, the mechanisms of action of S1PR agonists (fingolimod, ozanimod, etrasimod, and KRP-203), and their potential efficacy and safety for the treatment of patients with ulcerative colitis.Expert opinion: Selective S1P modulators have emerged to enlarge the efficacy and safety profile of this class of agents. Phase 3 programs should add the potential body of evidence to prove their benefit for the management of UC patients.Entities:
Keywords: Small-molecule drugs; sphingosine-1-phosphate; sphingosine-1-phosphate agonists; treatment; ulcerative colitis
Mesh:
Substances:
Year: 2020 PMID: 32093531 DOI: 10.1080/14712598.2020.1732919
Source DB: PubMed Journal: Expert Opin Biol Ther ISSN: 1471-2598 Impact factor: 4.388