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Article in Chinese | WPRIM | ID: wpr-286893

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of diallyl disulfide (DADS) on invasion and metastasis of human breast cancer MCF-7 cells and explore the possible mechanism.</p><p><b>METHODS</b>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.</p><p><b>RESULTS</b>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.</p><p><b>CONCLUSION</b>DADS can inhibit the invasion and metastasis of MCF-7 cells in vitro by down-regulating p38 activity.</p>


Subject(s)
Humans , Allyl Compounds , Pharmacology , Breast Neoplasms , Pathology , Cadherins , Metabolism , Disulfides , Pharmacology , Gene Expression Regulation, Neoplastic , MAP Kinase Signaling System , MCF-7 Cells , Matrix Metalloproteinase 9 , Metabolism , Mitogen-Activated Protein Kinase 11 , Metabolism , Neoplasm Invasiveness , Neoplasm Metastasis , Transforming Growth Factor beta1 , Pharmacology , Vimentin , Metabolism
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