Choi Suyong, Anderson Richard A
School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
EMBO J. 2017 Apr 13;36(8):967-969. doi: 10.15252/embj.201796827. Epub 2017 Mar 20.
ERK signaling and Akt signaling are inversely correlated in some cancers. Yet, the precise molecular mechanism for cross‐inhibition remains unclear. In this issue of , Pan (2017) show that when Akt is on, its phosphorylated cytoplasmic substrate FOXO1 turns off ERK activity by reshaping the Ras‐ERK scaffold IQGAP1.
在某些癌症中,细胞外信号调节激酶(ERK)信号传导和蛋白激酶B(Akt)信号传导呈负相关。然而,交叉抑制的确切分子机制仍不清楚。在本期杂志中,潘(2017年)表明,当Akt激活时,其磷酸化的细胞质底物叉头框蛋白O1(FOXO1)通过重塑Ras-ERK支架IQGAP1来关闭ERK活性。