Small-Molecule Targets in Immuno-Oncology

Cell Chem Biol. 2017 Sep 21;24(9):1148-1160. doi: 10.1016/j.chembiol.2017.08.019.

Abstract

Advances in understanding the role and molecular mechanisms underlying immune surveillance and control of (pre)malignancies is revolutionizing clinical practice in the treatment of cancer. Presently, multiple biologic drugs targeting the immune checkpoint proteins PD(L)1 or CTLA4 have been approved and/or are in advanced stages of clinical development for many cancers. In addition, combination therapy with these agents and other immunomodulators is being intensively explored with the aim of improving primary response rates or prolonging overall survival. The effectiveness of cancer immunotherapy with biologics is spurring research in alternate approaches including small-molecule-mediated targeting of intracellular pathways modulating the innate and adaptive immune response. This focus of this review is on some of the key intracellular pathways where the development of a small-molecule therapeutic is attractive, tractable, and potentially synergistic with extracellular biologic-mediated immune checkpoint blockade.

Publication types

  • Review

MeSH terms

  • CTLA-4 Antigen / antagonists & inhibitors
  • CTLA-4 Antigen / metabolism*
  • Humans
  • Immunologic Factors / chemistry
  • Immunologic Factors / pharmacology
  • Immunologic Factors / therapeutic use
  • Immunotherapy
  • Lymphocyte Activation / drug effects
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / metabolism
  • Neoplasms / immunology*
  • Neoplasms / therapy
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / antagonists & inhibitors
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor / metabolism*
  • Small Molecule Libraries / chemistry*
  • Small Molecule Libraries / pharmacology
  • Small Molecule Libraries / therapeutic use
  • Toll-Like Receptors / antagonists & inhibitors
  • Toll-Like Receptors / metabolism

Substances

  • CTLA-4 Antigen
  • CTLA4 protein, human
  • Immunologic Factors
  • Membrane Proteins
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • STING1 protein, human
  • Small Molecule Libraries
  • Toll-Like Receptors