Nuclear-targeted inhibition of NF-kappa B on MMP-9 production by N-2-(4-bromophenyl) ethyl caffeamide in human monocytic cells
Resource
CHEMICO-BIOLOGICAL INTERACTIONS, 184(3), 403-412
Journal
CHEMICO-BIOLOGICAL INTERACTIONS
Journal Volume
184
Journal Issue
3
Pages
403-412
Date Issued
2010
Date
2010
Author(s)
Chou, Yung-Chen
Sheu, Joen-Rong
Chung, Chi-Li
Chen, Chung-Yung
Lin, Fan-Li
Hsu, Ming-Jen
Kuo, Yueh-Hsiung
Hsiao, George
Abstract
Aberrant remodeling of the extracellular matrix occurs in many pathological processes, and its breakdown is mainly accomplished by matrix metalloproteinases (MMPs), which participate in the course of inflammation and tumor invasion. Nuclear factor-kappaB (NF-kappaB), a key transcription factor for the production of MMP-9, can be activated by various proinflammatory cytokines and promotes inflammation. In the present study, we investigated the intracellular mechanism for the inhibitory effects of an analogue of N-hydroxycinnamoylphenalkylamides, N-2-(4-bromophenyl) ethyl caffeamide (EK5), on tumor necrosis factor (TNF)-alpha stimulated expression of MMP-9 in a human monocytic cell line, THP-1. Our results show that TNF-alpha-induced expression of MMP-9 at both mRNA and protein levels was completely blocked by EK5 in a concentration-dependent (1-20microM) manner. We also found that EK5 markedly suppressed NF-kappaB signaling as detected by the NF-kappaB reporter gene assay but had no effects on the degradation of IkappaBalpha or translocation of NF-kappaB. Interestingly, chromatin immunoprecipitation results revealed that the association between p65 and MMP-9 promoter gene was completely abrogated by EK5, but the p65 phosphorylation was not affected. Overall, our findings suggest that EK5 inhibits MMP-9 production through the nuclear-targeted down-regulation of NF-kappaB signaling in human monocytic cells and this may provide a novel molecular basis of EK5 activity. Further studies are needed to verify its anti-inflammatory effects.
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Type
journal article
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