Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/61700
標題: Resveratrol analog-3,5,4 '-trimethoxy-trans-stilbene inhibits invasion of human lung adenocarcinoma cells by suppressing the MAPK pathway and decreasing matrix metalloproteinase-2 expression
作者: Yang, Ya-Ting
Weng, Chia-Jui
Ho, Chi-Tang
Yen, Gow-Chin
關鍵字: Invasion;MAPK signaling;MMP-2;Resveratrol;3,5,4;'-Trimethoxy-trans-stilbene;factor-kappa-b;urokinase-plasminogen activator;trans-resveratrol;cancer cells;signaling pathways;down-regulation;identification;apoptosis;growth;matrix-metalloproteinase-9
Project: Molecular Nutrition & Food Research, Volume 53, Issue 3, Page(s) 407-416.
摘要: 
Resveratrol (3,5,4'-trihydroxystilbene) is a natural polyphenol that presents various physiological activities. It has been reported that the methylated derivatives of resveratrol show better potential antifungal and antiproliferative activities than resveratrol. In the present Study, we investigated the inhibitory effect of 3,5,4'-trimethoxy-trans-stilbene (MR-3), a methylated derivative of resveratrol, on the invasion of A549 cells (a human lung adenocarcinoma cell line). We found that treatment with MR-3 at the concentration of 5 mu M resulted in antiadhesive, antimigratory, and antiinvasive activities oil A549 cells through the suppression of matrix metalloproteinase (MMP)-2 protein expression and transcriptional levels in a time-dependent manner. The suppression of MMP-2 expression by MR-3 led to an inhibition of A549 cell invasion by inactivating phosphorylation of SAPK/c-Jun N-terminal kinase (JNK) and p38 MAPK signaling pathways. A time-dependent inhibition of protein levels for p65, c-Jun, and c-Fos in the nucleus by MR-3 treatment was also observed. In conclusion, Our data demonstrate that the antiinvasive effects of MR-3 on A549 cells are likely mediated through the inhibition of phosphorylation of JNK and p38, as well as a reduction in the protein levels of nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1) in the nucleus, ultimately leading to downregulation of MMP-2 expression.
URI: http://hdl.handle.net/11455/61700
ISSN: 1613-4125
DOI: 10.1002/mnfr.200800123
Appears in Collections:食品暨應用生物科技學系

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