Protoflavonoids from ferns impair centrosomal integrity of tumor cells

Planta Med. 2011 Mar;77(5):461-6. doi: 10.1055/s-0030-1250407. Epub 2010 Oct 13.

Abstract

Six protoflavonoids, including two new compounds, were isolated during a large scale screening of fern extracts for original interaction with mitosis. The new compounds isolated from PHEGOPTERIS decursive-pinnata and EQUISETUM fluviatile were 2',3'-dihydroprotogenkwanone (1) and 2',3'-dihydro-2'-hydroxyprotoapigenone (2). Known compounds were: protoapigenone, protogenkwanone, protoapigenin, and 4'- O- β-D-glucopyranosyl protoapigenin. They showed a cytotoxic activity against HeLa cells at a micromolar level. IC₅₀ values were 2 µM for compound 1 > 10 µM for compound 2, and respectively 2.4, 0.6, > 10 µM for the known compounds. Their cytotoxic effects were associated with phenotypic changes never observed before and characterized by the loss of centrosomal γ-tubulin labelling in both mitotic and interphasic cells.

MeSH terms

  • Antineoplastic Agents, Phytogenic / toxicity*
  • Cell Survival / drug effects
  • Centrosome / drug effects*
  • Cyclohexanones / pharmacology
  • Ferns / chemistry*
  • Flavones / pharmacology
  • Flavonoids / toxicity*
  • HeLa Cells
  • Humans
  • Inhibitory Concentration 50
  • Mitosis / drug effects
  • Phenotype
  • Plant Extracts / toxicity*
  • Tubulin / drug effects*

Substances

  • Antineoplastic Agents, Phytogenic
  • Cyclohexanones
  • Flavones
  • Flavonoids
  • Plant Extracts
  • Tubulin
  • protoapigenone