4.7 Article

Suppression of PMA-induced tumor cell invasion and metastasis by aqueous extract isolated from Prunella vulgaris via the inhibition of NF-κB-dependent MMP-9 expression

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 48, 期 2, 页码 564-571

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2009.11.033

关键词

Prunella vulgans; Anti-metastatic; MMP-9; NF-kappa B; ERK1/2

资金

  1. Technology Development Program for Agriculture and Forestry [106011-03-1-SB010, 108159-3]
  2. Ministry for Food, Agriculture, Forestry and Fisheries, Republic of Korea
  3. National Research Foundation of Korea (NRF)
  4. Ministry of Education, Science and Technology [20090093815]
  5. Republic of Korea

向作者/读者索取更多资源

Matrix metalloproteinase-9 (MMP-9) plays an important role in the invasion and metastasis of cancer cells. In this study. we examined the inhibitory effects of tumor cell migration and invasion by aqueous extract isolated from Prunella vulgans (PVAE) using in vitro and in vivo assays. PVAE reduced PMA-induced activation of MMP-9 and further inhibited cell invasion and migration. PVAE suppressed PMA-enhanced expression of MMP-9 protein, mRNA and transcription activity levels through suppression of NF-kappa B activation without changing the tissue inhibitor of metalloproteinase level. PVAE inhibited PMA-induced NF-kappa B nuclear translocation, which is upstream of PMA-induced MMP-9 expression and invasion. Furthermore, pretreatment with NF-kappa B activation inhibitor inhibited the PMA-induced MMP-9 expression and activity. PVAE repressed the PMA-induced phosphorylation of ERK1/2, which is upstream signaling molecules in MMP-9 expression. We confirmed that the inhibitory effect of PVAE on lung metastasis and tumor cell growth using B16-F10 melanoma cells or B16-F1 melanoma cells in C57BL/6 mice. The oral administrations of PVAE reduced the lung metastasis and tumor cell growth by B16-F10 or B16-F1 melanoma cells. These results suggested that the anti-metastatic effect of PVAE is mediated through the suppression of MMP-9 expression by the inhibition of NF-kappa B via ERK1/2 signaling pathway as well as MMP-9 activity. (C) 2009 Elsevier Ltd. All rights reserved.

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