From the State Key Laboratory of Biotherapy, Section of Oncogene, West China Hospital, Sichuan University, Chengdu 610041.
the Laboratory of Stem Cell Biology, West China Hospital, Chengdu 610041.
J Biol Chem. 2014 Sep 5;289(36):24759-70. doi: 10.1074/jbc.M114.580738. Epub 2014 Jul 22.
Glycogen synthase kinase-3 (GSK3) has either tumor-suppressive roles or pro-tumor roles in different types of human tumors. A number of GSK3 targets in diverse signaling pathways have been uncovered, such as tuberous sclerosis complex subunit 2 and β-catenin. The O subfamily of forkhead/winged helix transcription factors (FOXO) is known as tumor suppressors that induce apoptosis. In this study, we find that FOXO binds to type I insulin-like growth factor receptor (IGF-IR) promoter and stimulates its transcription. GSK3 positively regulates the transactivation activity of FOXO and stimulates IGF-IR expression. Although kinase-dead GSK3β cannot up-regulate IGF-IR, the constitutively active GSK3β induces IGF-IR expression in a FOXO-dependent manner. Serum starvation or Akt inhibition leads to an increase in IGF-IR expression, which could be blunted by GSK3 inhibition. GSK3β knockdown or GSK3 inhibitor suppresses IGF-I-induced IGF-IR, Akt, and ERK1/2 phosphorylation. Moreover, knockdown of GSK3β or FOXO1/3/4 leads to a decrease in cellular proliferation and abrogates IGF-I-induced hepatoma cell proliferation. These results suggest that GSK3 and FOXO may positively regulate IGF-I signaling and hepatoma cell proliferation.
糖原合酶激酶-3(GSK3)在不同类型的人类肿瘤中具有抑瘤或促瘤作用。已经发现了许多不同信号通路中的 GSK3 靶标,如结节性硬化复合物亚基 2 和β-连环蛋白。叉头框/翼状螺旋转录因子(FOXO)的 O 亚家族被认为是诱导细胞凋亡的肿瘤抑制因子。在这项研究中,我们发现 FOXO 结合到 I 型胰岛素样生长因子受体(IGF-IR)启动子并刺激其转录。GSK3 正向调节 FOXO 的转录激活活性并刺激 IGF-IR 的表达。尽管激酶失活的 GSK3β 不能上调 IGF-IR,但组成性激活的 GSK3β 以 FOXO 依赖的方式诱导 IGF-IR 表达。血清饥饿或 Akt 抑制导致 IGF-IR 表达增加,GSK3 抑制可使其减弱。GSK3β 敲低或 GSK3 抑制剂抑制 IGF-I 诱导的 IGF-IR、Akt 和 ERK1/2 磷酸化。此外,敲低 GSK3β 或 FOXO1/3/4 导致细胞增殖减少,并阻断 IGF-I 诱导的肝癌细胞增殖。这些结果表明,GSK3 和 FOXO 可能正向调节 IGF-I 信号和肝癌细胞增殖。