Targeting Eph receptors with peptides and small molecules: progress and challenges

Semin Cell Dev Biol. 2012 Feb;23(1):51-7. doi: 10.1016/j.semcdb.2011.10.023. Epub 2011 Oct 25.

Abstract

The Eph receptors are a large family of receptor tyrosine kinases. Their kinase activity and downstream signaling ability are stimulated by the binding of cell surface-associated ligands, the ephrins. The ensuing signals are bidirectional because the ephrins can also transduce signals (known as reverse signals) following their interaction with Eph receptors. The ephrin-binding pocket in the extracellular N-terminal domain of the Eph receptors and the ATP-binding pocket in the intracellular kinase domain represent potential binding sites for peptides and small molecules. Indeed, a number of peptides and chemical compounds that target Eph receptors and inhibit ephrin binding or kinase activity have been identified. These molecules show promise as probes to study Eph receptor/ephrin biology, as lead compounds for drug development, and as targeting agents to deliver drugs or imaging agents to tumors. Current challenges are to find (1) small molecules that inhibit Eph receptor-ephrin interactions with high binding affinity and good lead-like properties and (2) selective kinase inhibitors that preferentially target the Eph receptor family or subsets of Eph receptors. Strategies that could also be explored include targeting additional Eph receptor interfaces and the ephrin ligands.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Humans
  • Lithocholic Acid / pharmacology
  • Molecular Targeted Therapy
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Peptides / pharmacology*
  • Peptides / therapeutic use
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Receptors, Eph Family / antagonists & inhibitors*
  • Receptors, Eph Family / metabolism*
  • Salicylates / pharmacology

Substances

  • Peptides
  • Protein Kinase Inhibitors
  • Salicylates
  • Lithocholic Acid
  • Receptors, Eph Family