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Suppressive effects of electrochemically reduced water on matrix metalloproteinase-2 activities and in vitro invasion of human fibrosarcoma HT1080 cells. | LitMetric

AI Article Synopsis

  • Hydrogen peroxide (H(2)O(2)) increases the expression of matrix metalloproteinase-2 (MMP-2) in various cell lines, promoting cell invasion.
  • Electrochemically reduced water (ERW) can reduce H(2)O(2) levels in human fibrosarcoma HT1080 cells, leading to decreased expression and activation of MMP-2, thereby reducing cell invasion.
  • The study found that ERW's effect on MMP-2 downregulation involves the p38 MAPK pathway, as inhibitors targeting this pathway significantly reduced MMP-2 gene expression.

Article Abstract

It has been demonstrated that hydrogen peroxide (H(2)O(2)) is directly associated with elevated matrix metalloproteinase-2 (MMP-2) expression in several cell lines. Electrochemically reduced water (ERW), produced near the cathode during electrolysis, and scavenges intracellular H(2)O(2) in human fibrosarcoma HT1080 cells. RT-PCR and zymography analyses revealed that when HT1080 cells were treated with ERW, the gene expression of MMP-2 and membrane type 1 MMP and activation of MMP-2 was repressed, resulting in decreased invasion of the cells into matrigel. ERW also inhibited H(2)O(2)-induced MMP-2 upregulation. To investigate signal transduction involved in MMP-2 downregulation, mitogen-activated protein kinase (MAPK)-specific inhibitors, SB203580 (p38 MAPK inhibitor), PD98059 (MAPK/extracellular regulated kinase kinase 1 inhibitor) and c-Jun NH(2)-terminal kinase inhibitor II, were used to block the MAPK signal cascade. MMP-2 gene expression was only inhibited by SB203580 treatment, suggesting a pivotal role of p38 MAPK in regulation of MMP-2 gene expression. Western blot analysis showed that ERW downregulated the phosphorylation of p38 both in H(2)O(2)-treated and untreated HT1080 cells. These results indicate that the inhibitory effect of ERW on tumor invasion is due to, at least in part, its antioxidative effect.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386386PMC
http://dx.doi.org/10.1007/s10616-012-9469-7DOI Listing

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