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首页> 外文期刊>Immunopharmacology and immunotoxicology >Hyul-Tong-Ryung suppresses PMA-induced MMP-9 expression by inhibiting AP-1-mediated gene expression via ERK 1/2 signaling pathway in MCF-7 human breast cancer cells.
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Hyul-Tong-Ryung suppresses PMA-induced MMP-9 expression by inhibiting AP-1-mediated gene expression via ERK 1/2 signaling pathway in MCF-7 human breast cancer cells.

机译:Hyul-Tong-Ryung通过抑制MCF-7人乳腺癌细胞中经由ERK 1/2信号通路的AP-1介导的基因表达来抑制PMA诱导的MMP-9表达。

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摘要

Our previous study has demonstrated that the methanol extract of Hyul-Tong-Ryung (HM) specifically suppresses the phorbol 12-myristate 13-acetate (PMA)-induced matrix metalloproteinase-9 (MMP-9) production through the inhibition of MMP-9 mRNA expression in MCF-7 human breast carcinoma cells. However, the molecular mechanisms involved in transcriptional suppression of MMP-9 by HM in PMA-induced MCF-7 cells are not known. In this study, we aimed to elucidate the molecular mechanisms involved in the inhibition of MMP-9 expression by HM in PMA-induced MCF-7 cells. The results of promoter assay and EMSA showed that HM specifically inhibits MMP-9 gene expression by blocking PMA-stimulated activation of activator protein-1 (AP-1). In addition, PMA-stimulated phosphorylation of extracellular signal regulated kinase 1/2 (ERK 1/2) was suppressed by HM treatment, whereas the phosphorylation of either c-Jun N-terminal kinase (JNK) or p38 mitogen-activated protein kinase (MAPK) was not affected. HM could inhibit the PMA-induced MMP-9 expression through suppression of the transcriptional activity of MMP-9 gene in MCF-7 cells. These results indicate that HM inhibits PMA-induced MMP-9 expression by blocking the activation of activator protein-1 (AP-1) via extracellular signal regulated kinase 1/2 (ERK 1/2) signaling pathway.
机译:我们以前的研究表明,Hyul-Tong-Ryung(HM)的甲醇提取物通过抑制MMP-9特异性抑制佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)诱导的基质金属蛋白酶9(MMP-9)的产生。 MCF-7人乳腺癌细胞中的mRNA表达。但是,尚不知道在PMA诱导的MCF-7细胞中HM抑制MMP-9转录的分子机制。在这项研究中,我们旨在阐明参与HM抑制PMA诱导的MCF-7细胞中MMP-9表达的分子机制。启动子分析和EMSA的结果表明,HM通过阻断PMA刺激的激活蛋白1(AP-1)激活而特异性抑制MMP-9基因表达。此外,HM处理可抑制PMA刺激的细胞外信号调节激酶1/2(ERK 1/2)的磷酸化,而c-Jun N末端激酶(JNK)或p38丝裂原活化蛋白激酶的磷酸化( MAPK)不受影响。 HM可以通过抑制MCF-7细胞中MMP-9基因的转录活性来抑制PMA诱导的MMP-9表达。这些结果表明,HM通过阻断细胞外信号调节激酶1/2(ERK 1/2)信号通路的激活蛋白1(AP-1)的激活来抑制PMA诱导的MMP-9表达。

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