[Diallyl disulfide inhibits invasion and metastasis of MCF-7 breast cancer cells in vitro by down-regulating p38 activity]

Nan Fang Yi Ke Da Xue Xue Bao. 2016 Jun;36(6):814-8.
[Article in Chinese]

Abstract

Objective: To investigate the effect of diallyl disulfide (DADS) on invasion and metastasis of human breast cancer MCF-7 cells and explore the possible mechanism.

Methods: MCF-7 cells treated with 100, 200, and 400 µmol/L of DADS for 24 h were examined for cell invasion and migration capacities using Transwell assay and wound healing assay, respectively. The protein expression of E-cadherin, vimentin, MMP-9 and p-p38 in the cells were detected with Western blotting. The effect of transforming growth factor-β1 (TGF-β1) as the agonist of p38 activity was tested in antagonizing the effects of DADS.

Results: DADS inhibited the invasion and migration of MCF-7 cells in a dose-dependent manner, down-regulated the protein expression of Vimentin and MMP-9 and up-regulated E-cadherin expression in the cells. Treatment with TGF-β1 to up-regulate p38 activity obviously antagonized the inhibitory effect of DADS on the invasion and metastasis of MCF-7 cells.

Conclusion: DADS can inhibit the invasion and metastasis of MCF-7 cells in vitro by down-regulating p38 activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allyl Compounds / pharmacology*
  • Antigens, CD
  • Breast Neoplasms / pathology*
  • Cadherins / metabolism
  • Disulfides / pharmacology*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • MAP Kinase Signaling System / drug effects*
  • MCF-7 Cells / drug effects
  • Matrix Metalloproteinase 9 / metabolism
  • Mitogen-Activated Protein Kinase 11 / metabolism*
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Transforming Growth Factor beta1 / pharmacology
  • Vimentin / metabolism

Substances

  • Allyl Compounds
  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • Disulfides
  • Transforming Growth Factor beta1
  • Vimentin
  • diallyl disulfide
  • Mitogen-Activated Protein Kinase 11
  • MMP9 protein, human
  • Matrix Metalloproteinase 9