| Literature DB >> 18985009 |
Ja Eun Kim1, Hong Sook Kim, Yong Jae Shin, Chang Seok Lee, Cheolhee Won, Sin Ae Lee, Jung Weon Lee, Youngsoo Kim, Jae Seung Kang, Sang Kyu Ye, Myung Hee Chung.
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.Entities:
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Year: 2008 PMID: 18985009 PMCID: PMC2679359 DOI: 10.3858/emm.2008.40.5.514
Source DB: PubMed Journal: Exp Mol Med ISSN: 1226-3613 Impact factor: 8.718