Retinoid agonist activities of synthetic geranyl geranoic acid derivatives

Biochem Biophys Res Commun. 1995 Apr 6;209(1):66-72. doi: 10.1006/bbrc.1995.1471.

Abstract

Micromolar concentrations of 4,5- didehydro geranyl geranoic acid (GGA) were able to induce up-regulation of retinoic acid receptor-beta gene expression in human hepatoma-derived cell line, HuH-7, to the same extent as all-trans RA. In chloramphenicol acetyl transferase (CAT) assay with retinoic acid response element-beta, GGA and 4,5-didehydro GGA were both positive, but 2,3-dihydro GGA was negative, even though these GGA derivatives have been reported to be all potent ligands for cellular retinoic-acid-binding protein(CRABP). However, 10,11,14,15- tetrahydro- 4,5- didehydro GGA, a compound without any affinity for CRABP, transactivated CAT gene expression. On the other hand, only GGA and 4,5-didehydro GGA were active to induce CAT gene expression through retinoid X response element of cellular retinol binding protein, type II gene. We show for the first time that chemically synthesized acyclic organic acids are potential agonists of natural retinoids.

MeSH terms

  • Chloramphenicol O-Acetyltransferase / genetics
  • Diterpenes / chemistry
  • Diterpenes / pharmacology*
  • Gene Expression Regulation / drug effects
  • Humans
  • Receptors, Retinoic Acid / genetics
  • Retinoids / agonists*
  • Retinoids / pharmacology
  • Tumor Cells, Cultured

Substances

  • Diterpenes
  • Receptors, Retinoic Acid
  • Retinoids
  • retinoic acid binding protein II, cellular
  • retinoic acid receptor beta
  • geranylgeranic acid
  • Chloramphenicol O-Acetyltransferase