Department of Biochemistry, Medical College of Georgia, Augusta, Georgia, USA.
Cancer Res. 2009 Dec 15;69(24):9228-35. doi: 10.1158/0008-5472.CAN-09-1950.
Cell migration is a critical step in cancer cell invasion. Recent studies have implicated the importance of the extracellular signal-regulated kinase (ERK) signaling pathway in cancer cell migration. However, the mechanism associated with ERK-regulated cell migration is poorly understood. Using a panel of breast cancer cell lines, we detected an excellent correlation between ERK activity and cell migration. Interestingly, we noticed that a 48-hour treatment with U0126 [specific mitogen-activated protein/ERK kinase (MEK)-1/2 inhibitor] was needed to significantly inhibit breast cancer cell migration, whereas this inhibitor blocked ERK activity within 1 hour. This observation suggests that ERK-dependent gene expression, rather than direct ERK signaling, is essential for cell migration. With further study, we found that ERK activity promoted the expression of the activator protein-1 (AP1) components Fra-1 and c-Jun, both of which were necessary for cell migration. Combination of U0126 treatment and Fra-1/c-Jun knockdown did not yield further reduction in cell migration than either alone, indicating that ERKs and Fra-1/c-Jun act by the same mechanism to facilitate cell migration. In an attempt to investigate the role of Fra-1/c-Jun in cell migration, we found that the ERK-Fra-1/c-Jun axis regulated slug expression in an AP1-dependent manner. Moreover, the occurrence of U0126-induced migratory inhibition coincided with slug reduction, and silencing slug expression abrogated breast cancer cell migration. These results suggest an association between ERK-regulated cell migration and slug expression. Indeed, cell migration was not significantly inhibited by U0126 treatment or Fra-1/c-Jun silencing in cells expressing slug transgene. Our study suggests that the ERK pathway regulates breast cancer cell migration by maintaining slug expression.
细胞迁移是癌细胞侵袭的关键步骤。最近的研究表明细胞外信号调节激酶(ERK)信号通路在癌细胞迁移中具有重要作用。然而,ERK 调节细胞迁移的机制尚不清楚。我们使用一组乳腺癌细胞系检测到 ERK 活性与细胞迁移之间存在极好的相关性。有趣的是,我们注意到 U0126(特异性丝裂原激活蛋白/ERK 激酶(MEK)-1/2 抑制剂)的 48 小时处理可显著抑制乳腺癌细胞迁移,而该抑制剂在 1 小时内即可阻断 ERK 活性。这一观察结果表明,ERK 依赖性基因表达而不是直接的 ERK 信号对于细胞迁移是必需的。进一步研究发现,ERK 活性促进了激活蛋白-1(AP1)组件 Fra-1 和 c-Jun 的表达,两者均是细胞迁移所必需的。U0126 处理与 Fra-1/c-Jun 敲低的组合并未比单独处理产生进一步降低细胞迁移的效果,这表明 ERK 和 Fra-1/c-Jun 通过相同的机制来促进细胞迁移。为了研究 Fra-1/c-Jun 在细胞迁移中的作用,我们发现 ERK-Fra-1/c-Jun 轴以依赖于 AP1 的方式调节 slug 的表达。此外,U0126 诱导的迁移抑制的发生与 slug 减少相吻合,沉默 slug 表达可消除乳腺癌细胞迁移。这些结果表明 ERK 调节的细胞迁移与 slug 表达之间存在关联。事实上,在表达 slug 转基因的细胞中,U0126 处理或 Fra-1/c-Jun 沉默并没有显著抑制细胞迁移。我们的研究表明 ERK 通路通过维持 slug 表达来调节乳腺癌细胞迁移。