Effects of artonin e on migration and invasion capabilities of human lung cancer cells

Anticancer Res. 2013 Aug;33(8):3079-88.

Abstract

Background: Knowledge regarding substances that attenuate motility of cancer cells has gathered significant attention, as they benefit the development of novel anticancer strategies. The anti-migration and anti-invasion activities of artonin E, extracted from bark of Artocarpus gomezianus, were investigated in lung cancer cells in this study.

Materials and methods: Cytotoxicity and antiproliferative effects of artonin E were examined by 3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Migration and invasion assays were performed on H460, H23, A549 and H292 human lung cancer cells. Cell morphology was determined by phalloidin-rhodamine staining. Motility-related proteins were investigated by western blotting.

Results: Artonin E exhibited anti-migration and anti-invasion activities in H460 cells. Cell morphology revealed that treatment of the cells with non-toxic concentrations of artonin E resulted in a decrease of activated focal adhesion kinase (FAK), downstream protein kinase B (AKT) activation, and Cell division cycle-42 (CDC42), all of which were associated with the anti-motility effect of this compound. Artonin E inhibited invasion and migration of other lung cancer cells, namely H292, H23 and A549 cells.

Conclusion: These results suggest that artonin E may be a promising candidate for anti-metastasis use.

Keywords: A549; H23; H292 cells; H460; Metastasis; artonin E; invasion; lung cancer cells; migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / enzymology
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Caveolin 1 / metabolism
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Cell Movement / drug effects*
  • Cell Survival / drug effects
  • Flavonoids / chemistry
  • Flavonoids / pharmacology*
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Humans
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / pathology*
  • Neoplasm Invasiveness
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pseudopodia / drug effects
  • Pseudopodia / metabolism
  • Signal Transduction / drug effects
  • cdc42 GTP-Binding Protein / metabolism

Substances

  • Caveolin 1
  • Flavonoids
  • artonin E
  • Focal Adhesion Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-akt
  • cdc42 GTP-Binding Protein