| Literature DB >> 25053419 |
Xiaodong Huo1, Shu Liu1, Ting Shao1, Hui Hua2, Qingbin Kong1, Jiao Wang3, Ting Luo4, Yangfu Jiang5.
Abstract
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.Entities:
Keywords: Cancer; FOXO; Glycogen Synthase Kinase 3 (GSK-3); Insulin-like Growth Factor (IGF); Receptor Tyrosine Kinase
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Year: 2014 PMID: 25053419 PMCID: PMC4155645 DOI: 10.1074/jbc.M114.580738
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157