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LYR71, a derivative of trimeric resveratrol, inhibits tumorigenesis by blocking STAT3-mediated matrix metalloproteinase 9 expression
Experimental & Molecular Medicine ; : 514-522, 2008.
Article in English | WPRIM | ID: wpr-84651
ABSTRACT
Tumor migration/invasion is the main cause of tumor progression and STAT3 is needed to enhance tumor migration/invasion by up-regulating MMP-9. Thus, agents that inhibit STAT3 activation may be used as an anticancer drug. We present herein that 6-methyl-2-propylimino-6, 7-dihydro-5H-benzo [1, 3]-oxathiol- 4-one (LYR71) , a derivative of trimeric resveratrol, has an anticancer activity through inhibition of STAT3 activation. We found that LYR71 suppressed STAT3 activation and inhibited the expression and activity of MMP-9 in RANTES-stimulated breast cancer cells. In addition, LYR71 reduced RANTES-induced MMP-9 transcripts by blocking STAT3 recruitment, dissociating p300 and deacetylating histone H3 and H4 on the MMP-9 promoter. Furthermore, LYR71 inhibited tumor migration/invasion in RANTES-treated breast cancer cells and consequently blocked tumor progression in tumor-bearing mice. Taken together, the results of this study suggest that LYR71 can be therapeutically useful due to the inhibition effect of STAT3-mediated MMP-9 expression in breast cancer cells.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphorylation / Stilbenes / Breast Neoplasms / Immunohistochemistry / Molecular Structure / Gene Expression / Cell Movement / Cell Survival / Blotting, Western / Bridged Bicyclo Compounds, Heterocyclic Type of study: Prognostic study Limits: Animals / Female / Humans Language: English Journal: Experimental & Molecular Medicine Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phosphorylation / Stilbenes / Breast Neoplasms / Immunohistochemistry / Molecular Structure / Gene Expression / Cell Movement / Cell Survival / Blotting, Western / Bridged Bicyclo Compounds, Heterocyclic Type of study: Prognostic study Limits: Animals / Female / Humans Language: English Journal: Experimental & Molecular Medicine Year: 2008 Type: Article