A novel anticancer effect of butein: inhibition of invasion through the ERK1/2 and NF-kappa B signaling pathways in bladder cancer cells

FEBS Lett. 2008 Jun 11;582(13):1821-8. doi: 10.1016/j.febslet.2008.04.046. Epub 2008 May 8.

Abstract

There is increasing evidence that epithelial-mesenchymal transition (EMT) plays a critical role in cancer metastasis. Butein is a polyphenolic compound, which has been found to exhibit anti-proliferation effects on cancer cells. Here, we report that in addition to its function as an anti-proliferation agent, butein can inhibit migration and invasion through the ERK1/2 and NF-kappaB signaling pathways in human bladder cancer cells, and this inhibitory effect may be associated with reversal of EMT. These results were further confirmed by RNAi-mediated suppression of NF-kappaB, which partly reverses EMT and inhibits cell invasive ability in vitro. These results suggest a novel function of butein as an invasion inhibitor in bladder cancer.

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Chalcones / pharmacology*
  • Down-Regulation
  • Gene Expression / drug effects
  • Humans
  • Mesoderm / pathology
  • Mitogen-Activated Protein Kinase 1 / metabolism*
  • Mitogen-Activated Protein Kinase 3 / metabolism*
  • Neoplasm Invasiveness
  • Phenotype
  • Phosphorylation / drug effects
  • RNA Interference
  • Signal Transduction / drug effects
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism*
  • Urinary Bladder Neoplasms / metabolism*
  • Urinary Bladder Neoplasms / pathology

Substances

  • Antineoplastic Agents
  • Chalcones
  • Transcription Factor RelA
  • butein
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3