The antineoplastic properties of FTY720: evidence for the repurposing of fingolimod

J Cell Mol Med. 2015 Oct;19(10):2329-40. doi: 10.1111/jcmm.12635. Epub 2015 Jul 14.

Abstract

Almost all drugs approved for use in humans possess potentially beneficial 'off-target' effects in addition to their principal activity. In some cases this has allowed for the relatively rapid repurposing of drugs for other indications. In this review we focus on the potential for re-purposing FTY720 (also known as fingolimod, Gilenya(™)), an immunomodulatory drug recently approved for the treatment of multiple sclerosis (MS). The therapeutic benefit of FTY720 in MS is largely attributed to the immunosuppressive effects that result from its modulation of sphingosine 1-phosphate receptor signalling. However, this drug has also been shown to inhibit other cancer-associated signal transduction pathways in part because of its structural similarity to sphingosine, and consequently shows efficacy as an anti-cancer agent both in vitro and in vivo. Here, we review the effects of FTY720 on signal transduction pathways and cancer-related cellular processes, and discuss its potential use as an anti-cancer drug.

Keywords: FTY720; S1P; apoptosis; cancer; cytotoxicity; fingolimod; sphingosine analogue.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Drug Delivery Systems
  • Drug Repositioning*
  • Fingolimod Hydrochloride / pharmacology*
  • Humans
  • Phenotype
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • Fingolimod Hydrochloride