1] Markey Cancer Center, College of Medicine, University of Kentucky, Lexington, KY, USA [2] Department of Molecular and Biomedical Pharmacology, College of Medicine, University of Kentucky, Lexington, KY, USA.
1] Markey Cancer Center, College of Medicine, University of Kentucky, Lexington, KY, USA [2] Department of Surgery, College of Medicine, University of Kentucky, Lexington, KY, USA.
Oncogene. 2014 Apr 3;33(14):1828-39. doi: 10.1038/onc.2013.122. Epub 2013 Apr 29.
The mitogen-activated extracellular signal-regulated kinase/extracellular signal-regulated kinase (MEK/ERK) and phosphatidylinositol 3-kinase (PI3K)/AKT pathways are often concurrently activated by separate genetic alterations in colorectal cancer (CRC), which is associated with CRC progression and poor survival. However, how activating both pathways is required for CRC metastatic progression remains unclear. Our recent study showed that both ERK and AKT signaling are required to activate eukaryotic translation initiation factor 4E (eIF4E)-initiated cap-dependent translation via convergent regulation of the translational repressor 4E-binding protein 1 (4E-BP1) for maintaining CRC transformation. Here, we identified that the activation of cap-dependent translation by cooperative ERK and AKT signaling is critical for promotion of CRC motility and metastasis. In CRC cells with coexistent mutational activation of ERK and AKT pathways, inhibition of either MEK or AKT alone showed limited activity in inhibiting cell migration and invasion, but combined inhibition resulted in profound effects. Genetic blockade of the translation initiation complex by eIF4E knockdown or expression of a dominant active 4E-BP1 mutant effectively inhibited migration, invasion and metastasis of CRC cells, whereas overexpression of eIF4E or knockdown of 4E-BP1 had the opposite effect and markedly reduced their dependence on ERK and AKT signaling for cell motility. Mechanistically, we found that these effects were largely dependent on the increase in mammalian target of rapamycin complex 1 (mTORC1)-mediated survivin translation by ERK and AKT signaling. Despite the modest effect of survivin knockdown on tumor growth, reduction of the translationally regulated survivin profoundly inhibited motility and metastasis of CRC. These findings reveal a critical mechanism underlying the translational regulation of CRC metastatic progression, and suggest that targeting cap-dependent translation may provide a promising treatment strategy for advanced CRC.
丝裂原活化的细胞外信号调节激酶/细胞外信号调节激酶(MEK/ERK)和磷脂酰肌醇 3-激酶(PI3K)/AKT 途径通常在结直肠癌(CRC)中通过独立的遗传改变同时被激活,这与 CRC 的进展和不良预后相关。然而,激活这两条途径对于 CRC 转移进展的必要性仍不清楚。我们最近的研究表明,ERK 和 AKT 信号都需要通过收敛调节翻译抑制剂 4E 结合蛋白 1(4E-BP1)来激活真核起始因子 4E(eIF4E)起始的帽依赖性翻译,以维持 CRC 转化。在这里,我们确定了协同 ERK 和 AKT 信号激活帽依赖性翻译对于促进 CRC 运动性和转移的关键性。在同时存在 ERK 和 AKT 途径突变激活的 CRC 细胞中,单独抑制 MEK 或 AKT 显示出对抑制细胞迁移和侵袭的有限活性,但联合抑制则产生深远的效果。通过 eIF4E 敲低或表达显性激活的 4E-BP1 突变体抑制翻译起始复合物,有效地抑制 CRC 细胞的迁移、侵袭和转移,而 eIF4E 的过表达或 4E-BP1 的敲低则产生相反的效果,并显著降低它们对 ERK 和 AKT 信号的细胞运动依赖性。从机制上讲,我们发现这些效果在很大程度上依赖于 ERK 和 AKT 信号对哺乳动物雷帕霉素靶蛋白复合物 1(mTORC1)介导的存活素翻译的增加。尽管存活素敲低对肿瘤生长的影响不大,但翻译调节的存活素的减少则显著抑制了 CRC 的运动性和转移。这些发现揭示了 CRC 转移进展的翻译调控的关键机制,并表明靶向帽依赖性翻译可能为晚期 CRC 提供一种有前途的治疗策略。