Structure-activity relationship analyses of glycyrrhetinic acid derivatives as anticancer agents

Mini Rev Med Chem. 2011 Sep;11(10):881-7. doi: 10.2174/138955711796575443.

Abstract

Cancer cell resistance to kinase inhibitors and targeted agents, acquisition of a multidrug-resistant (MDR) phenotype and/or intrinsic resistance to apoptosis prevent effective treatment in about 50% of solid cancers in adults, and the percentage is even higher in children. Glycyrrhetinic acid (GA) and some of its derivatives may offer hope in combating cancer types associated with poor prognoses. Some GA derivatives are indeed able to target both the proteasome and peroxisome proliferator-activated receptors (PPARs), two proteins that play major roles in cancer cell biology but are not related to MDR and/or apoptosis-related resistance phenotypes.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects
  • Drug Resistance, Neoplasm
  • Drug Screening Assays, Antitumor
  • Glycyrrhetinic Acid / analogs & derivatives*
  • Glycyrrhetinic Acid / pharmacology
  • Humans
  • PPAR gamma / antagonists & inhibitors
  • PPAR gamma / metabolism
  • Proteasome Endopeptidase Complex / metabolism
  • Proteasome Inhibitors
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • PPAR gamma
  • Proteasome Inhibitors
  • Proteasome Endopeptidase Complex
  • Glycyrrhetinic Acid