Optimizing the aryl-triazole of cjoc42 for enhanced gankyrin binding and anti-cancer activity

Bioorg Med Chem Lett. 2020 Sep 1;30(17):127372. doi: 10.1016/j.bmcl.2020.127372. Epub 2020 Jul 2.

Abstract

Gankyrin is an oncoprotein overexpressed in numerous cancer types and appears to play a key role in regulating cell proliferation, cell growth, and cell migration. These roles are largely due to gankyrin's protein-protein interaction with the 26S proteasome. We previously published a study exploring the aryl sulfonate ester of cjoc42 in an effort to enhance gankyrin binding and inhibit cancer cell proliferation. In order to further improve the gankyrin binding ability of the cjoc42 scaffold, an extensive SAR for the aryl-triazole moiety of cjoc42 was developed. Our cjoc42 derivatives exhibited enhanced gankyrin binding, as well as enhanced antiproliferative activity against Hep3B, HepG2, A549, and MDA-MB-231 cancer cell lines.

Keywords: Antiproliferation; Breast cancer; Gankyrin; Liver cancer; Lung cancer; Protein-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology
  • Benzenesulfonates / chemistry*
  • Benzenesulfonates / metabolism
  • Benzenesulfonates / pharmacology
  • Binding Sites
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Drug Screening Assays, Antitumor
  • Humans
  • Molecular Dynamics Simulation
  • Proteasome Endopeptidase Complex / chemistry
  • Proteasome Endopeptidase Complex / metabolism*
  • Protein Binding
  • Proto-Oncogene Proteins / chemistry
  • Proto-Oncogene Proteins / metabolism*
  • Structure-Activity Relationship
  • Triazoles / chemistry*
  • Triazoles / metabolism
  • Triazoles / pharmacology

Substances

  • Antineoplastic Agents
  • Benzenesulfonates
  • PSMD10 protein, human
  • Proto-Oncogene Proteins
  • Triazoles
  • cjoc42 compound
  • Proteasome Endopeptidase Complex