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在 MCF-7 人乳腺癌细胞中,草苁蓉通过 ERK1/2 信号通路抑制 PMA 诱导的 MMP-9 表达,从而抑制 AP-1 介导的基因表达。

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.

机构信息

College of Natural Resources and Life Science, BK21 Center for Silver-Bio Industrialization, Dong-A University, Busan, South Korea.

出版信息

Immunopharmacol Immunotoxicol. 2010 Dec;32(4):600-6. doi: 10.3109/08923971003610817. Epub 2010 Feb 4.

Abstract

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.

摘要

我们之前的研究表明,虎杖龙根甲醇提取物(HM)通过抑制 MCF-7 人乳腺癌细胞中 MMP-9 mRNA 的表达,特异性抑制佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)诱导的基质金属蛋白酶-9(MMP-9)产生。然而,HM 通过 PMA 诱导的 MCF-7 细胞中 MMP-9 的转录抑制涉及的分子机制尚不清楚。在这项研究中,我们旨在阐明 HM 在 PMA 诱导的 MCF-7 细胞中抑制 MMP-9 表达的分子机制。启动子测定和电泳迁移率变动分析(EMSA)的结果表明,HM 通过阻断 PMA 刺激的激活蛋白-1(AP-1)的激活,特异性抑制 MMP-9 基因表达。此外,HM 处理抑制了 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(MAPK)的磷酸化不受影响。HM 可以通过抑制 MMP-9 基因的转录活性来抑制 MCF-7 细胞中 PMA 诱导的 MMP-9 表达。这些结果表明,HM 通过细胞外信号调节激酶 1/2(ERK 1/2)信号通路抑制激活蛋白-1(AP-1)的激活来抑制 PMA 诱导的 MMP-9 表达。

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