Activity-based protein profiling reveals GSTO1 as the covalent target of piperlongumine and a promising target for combination therapy for cancer

Chem Commun (Camb). 2019 Apr 9;55(30):4407-4410. doi: 10.1039/c9cc00917e.

Abstract

Through systematic target identification for piperlongumine, a cancer-selective killing molecule, we identified GSTO1 as its major covalent target for cancer cell death induction. We also reveal that GSTO1 inhibition is a promising combination strategy with other anti-cancer agents by drug combination screening in which piperlongumine exhibits broad-spectrum synergistic effects with a large proportion of the tested anti-cancer agents, especially with PI3K/Akt/mTOR pathway inhibitors.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Dioxolanes / pharmacology*
  • Drug Synergism
  • Glutathione Transferase / antagonists & inhibitors
  • Glutathione Transferase / chemistry
  • Glutathione Transferase / metabolism*
  • Humans
  • Models, Molecular
  • Molecular Targeted Therapy / methods*
  • Protein Conformation

Substances

  • Antineoplastic Agents
  • Dioxolanes
  • GSTO1 protein, human
  • Glutathione Transferase
  • piperlongumine