Dioscorea nipponica Makino inhibits migration and invasion of human oral cancer HSC-3 cells by transcriptional inhibition of matrix metalloproteinase-2 through modulation of CREB and AP-1 activity

Food Chem Toxicol. 2012 Mar;50(3-4):558-66. doi: 10.1016/j.fct.2011.12.016. Epub 2011 Dec 19.

Abstract

Oral cancer mortality has increased during the last decade due to the difficulties in treating related metastasis. Dioscorea nipponica Makino, a popular folk medicine, exerts anti-obesity and anti-inflammation properties. However, the effect of this folk medicine on metastasis of oral cancer has yet to be fully elucidated. The present study demonstrates that D. nipponica extracts (DNE), at a range of concentrations (0-50 μg/mL), concentration-dependently inhibited migration/invasion capacities of human oral cancer cells, HSC-3, without cytotoxic effects. The anti-migration effect of DNE was also observed in two other OSCC cell lines, Ca9-22 and Cal-27. Zymography, real time PCR, and Western blotting analyses revealed that DNE inhibited matrix metalloproteinase-2 (MMP-2) enzyme activity, and RNA and protein expression. The inhibitory effects of DNE on MMP-2 proceeded by up-regulating tissue inhibitor of metalloproteinase-2 (TIMP-2), as well as suppressing nuclear translocation and DNA binding activity of cAMP response element-binding (CREB) and activating protein-1 (AP-1) on the MMP-2 promoter in HSC-3 cells. In conclusion, DNE inhibited the invasion of oral cancer cells and may have potential use as a chemopreventive agent against oral cancer metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • DNA Primers
  • Dioscorea / chemistry*
  • Flow Cytometry
  • Humans
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase Inhibitors*
  • Mouth Neoplasms / enzymology
  • Mouth Neoplasms / pathology*
  • Plant Extracts / pharmacology*
  • Real-Time Polymerase Chain Reaction
  • Transcription Factor AP-1 / metabolism*
  • Transcription, Genetic*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • DNA Primers
  • Matrix Metalloproteinase Inhibitors
  • Plant Extracts
  • Transcription Factor AP-1
  • Matrix Metalloproteinase 2