Design, synthesis and biological evaluation of tetrazole-containing RXRα ligands as anticancer agents

Eur J Med Chem. 2019 Feb 15:164:562-575. doi: 10.1016/j.ejmech.2018.12.036. Epub 2018 Dec 19.

Abstract

Nuclear receptor RXRα plays an important role in many biological and pathological processes. The nongenomic action of RXRα is implicated in many cancers. K-8008, a non-canonical RXRα ligand derived from sulindac, inhibits the TNFα-activated PI3K/AKT pathway by mediating the interaction between a truncated form of RXRα (tRXRα) and the p85α regulatory subunit of PI3K and exerts potent anticancer activity in animal model. Herein we report our studies of a novel series of K-8008 analogs as potential anticancer agents targeting RXRα. Two compounds 8b and 18a were identified to have slightly stronger binding to RXRα and improved apoptotic activities in breast cancer cells.

Keywords: Anticancer activity; Bioisostere; PI3K/AKT pathway; RXRα; RXRα modulator.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Apoptosis / drug effects
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Drug Design*
  • Humans
  • Ligands
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Retinoid X Receptor alpha*
  • Tetrazoles / chemical synthesis
  • Tetrazoles / chemistry
  • Tetrazoles / metabolism
  • Tetrazoles / pharmacology*
  • Tumor Necrosis Factor-alpha

Substances

  • Antineoplastic Agents
  • Ligands
  • Retinoid X Receptor alpha
  • Tetrazoles
  • Tumor Necrosis Factor-alpha
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt