Topoisomerase I inhibition and cytotoxicity of licochalcones A and E from Glycyrrhiza inflata

Arch Pharm Res. 2007 Mar;30(3):313-6. doi: 10.1007/BF02977611.

Abstract

Licochalcones A (1) and E (2), retrochalcones or reversely constructed chalcones, isolated from the roots of Glycyrrhiza inflata, were evaluated for their cytotoxicities against four different human tumor cell lines; A549 (lung), SK-OV-3 (ovarian), SK-MEL-2 (melanoma) and HCT-15 (colon), using the sulforhodamine B (SRB) assay. The effects of these compounds toward the DNA topoisomerase I (topo I) inhibitory activity were also measured using the supercoiled DNA unwinding assay. All compounds showed moderate cytotoxicities against the four different human tumor cell lines and inhibited the topo I activity in dose-dependent manners. The inhibition of topo I by licochalcones A (1) and E (2) may explain the cytotoxicities of these compounds against the human tumor cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Line
  • Chalcones / pharmacology*
  • Enzyme Inhibitors / pharmacology*
  • Glycyrrhiza / chemistry*
  • Humans
  • Structure-Activity Relationship
  • Topoisomerase I Inhibitors*

Substances

  • Antineoplastic Agents, Phytogenic
  • Chalcones
  • Enzyme Inhibitors
  • Topoisomerase I Inhibitors
  • licochalcone E
  • licochalcone A