Suppr超能文献

鸟氨酸脱羧酶过表达增强细胞外信号调节激酶(ERK)和p38磷酸化以及基质金属蛋白酶-2的表达。

Ornithine decarboxylase overexpression enhances ERK and p38 phosphorylation and matrix metalloproteinase-2 expression.

作者信息

Nemoto Takahiro, Kubota Shunichiro

机构信息

Department of Physiological Chemistry and Metabolism, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Tokyo 113-0033, Japan.

出版信息

Cell Biol Int. 2007 Feb;31(2):141-7. doi: 10.1016/j.cellbi.2006.09.019. Epub 2006 Sep 28.

Abstract

In the present study, we investigated the relationship between ornithine decarboxylase, MAP kinase, and MMP-2 expression in vitro. Overexpression of ornithine decarboxylase cDNA induced MMP-2 expression both at mRNA and protein levels. Promoter analysis and gel shift assay showed that p53 and Ets-1 were involved in MMP-2 expression in ornithine decarboxylase overexpressing transfectants. Erk and p38 MAP kinase were significantly activated. Using specific inhibitors of MEK and p38, we clarified that MMP-2 expression was induced via both Erk and p38 MAP kinase signaling pathways. This is the first report showing the existence of a causal relationship between ornithine decarboxylase expression, Erk and p38 MAP kinase activation, and MMP-2 expression.

摘要

在本研究中,我们在体外研究了鸟氨酸脱羧酶、丝裂原活化蛋白激酶(MAP激酶)和基质金属蛋白酶-2(MMP-2)表达之间的关系。鸟氨酸脱羧酶cDNA的过表达在mRNA和蛋白质水平均诱导了MMP-2的表达。启动子分析和凝胶迁移试验表明,p53和Ets-1参与了过表达鸟氨酸脱羧酶的转染细胞中MMP-2的表达。细胞外信号调节激酶(Erk)和p38 MAP激酶被显著激活。使用MEK和p38的特异性抑制剂,我们阐明MMP-2的表达是通过Erk和p38 MAP激酶信号通路诱导的。这是首份表明鸟氨酸脱羧酶表达、Erk和p38 MAP激酶激活与MMP-2表达之间存在因果关系的报告。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验