Medical University of South Carolina, Charleston, SC, United States.
Adv Cancer Res. 2018;138:99-142. doi: 10.1016/bs.acr.2018.02.004. Epub 2018 Mar 2.
The extracellular-regulated kinases ERK1 and ERK2 are evolutionarily conserved, ubiquitous serine-threonine kinases that are involved in regulating cellular signaling in both normal and pathological conditions. Their expression is critical for development and their hyperactivation is a major factor in cancer development and progression. Since their discovery as one of the major signaling mediators activated by mitogens and Ras mutation, we have learned much about their regulation, including their activation, binding partners and substrates. In this review I will discuss some of what has been discovered about the members of the Ras to ERK pathway, including regulation of their activation by growth factors and cell adhesion pathways. Looking downstream of ERK activation I will also highlight some of the many ERK substrates that have been discovered, including those involved in feedback regulation, cell migration and cell cycle progression through the control of transcription, pre-mRNA splicing and protein synthesis.
细胞外调节激酶 ERK1 和 ERK2 是进化上保守的、普遍存在的丝氨酸-苏氨酸激酶,参与调节正常和病理条件下的细胞信号转导。它们的表达对于发育至关重要,其过度激活是癌症发生和发展的主要因素。自从它们被发现作为丝裂原和 Ras 突变激活的主要信号转导介质之一以来,我们已经了解了很多关于它们的调节,包括它们的激活、结合伙伴和底物。在这篇综述中,我将讨论 Ras 到 ERK 途径的一些成员,包括生长因子和细胞黏附途径对其激活的调节。在 ERK 激活的下游,我还将重点介绍一些已经发现的许多 ERK 底物,包括那些参与反馈调节、细胞迁移和细胞周期通过转录、前体 mRNA 剪接和蛋白质合成的控制进展的底物。