Oncogenic protein interfaces: small molecules, big challenges

Nat Rev Cancer. 2014 Apr;14(4):248-62. doi: 10.1038/nrc3690. Epub 2014 Mar 13.

Abstract

Historically, targeting protein-protein interactions with small molecules was not thought possible because the corresponding interfaces were considered mostly flat and featureless and therefore 'undruggable'. Instead, such interactions were targeted with larger molecules, such as peptides and antibodies. However, the past decade has seen encouraging breakthroughs through the refinement of existing techniques and the development of new ones, together with the identification and exploitation of unexpected aspects of protein-protein interaction surfaces. In this Review, we describe some of the latest techniques to discover modulators of protein-protein interactions and how current drug discovery approaches have been adapted to successfully target these interfaces.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Binding Sites
  • Drug Screening Assays, Antitumor
  • Humans
  • Molecular Docking Simulation
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Oncogene Proteins / chemistry*
  • Oncogene Proteins / metabolism
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Interaction Maps
  • Surface Properties

Substances

  • Antineoplastic Agents
  • Oncogene Proteins