The design and development of covalent protein-protein interaction inhibitors for cancer treatment

J Hematol Oncol. 2020 Mar 30;13(1):26. doi: 10.1186/s13045-020-00850-0.

Abstract

Protein-protein interactions (PPIs) are central to a variety of biological processes, and their dysfunction is implicated in the pathogenesis of a range of human diseases, including cancer. Hence, the inhibition of PPIs has attracted significant attention in drug discovery. Covalent inhibitors have been reported to achieve high efficiency through forming covalent bonds with cysteine or other nucleophilic residues in the target protein. Evidence suggests that there is a reduced risk for the development of drug resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious diseases. Recent improvements in structural biology and chemical reactivity have enabled the design and development of potent and selective covalent PPI inhibitors. In this review, we will highlight the design and development of therapeutic agents targeting PPIs for cancer therapy.

Keywords: Cancer therapy; Covalent inhibitors; Protein-protein interaction.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Drug Design*
  • Drug Development* / methods
  • Humans
  • Models, Molecular
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Protein Interaction Maps / drug effects*

Substances

  • Antineoplastic Agents