| Literature DB >> 25311538 |
Shanshan Xu1, Minghong Tong2, Jingqin Huang1, Yue Zhang3, Yongxia Qiao4, Wenhao Weng1, Weiwei Liu1, Jiayi Wang5, Fenyong Sun6.
Abstract
Tribbles homolog 2 (TRIB2) is specifically regulated by Wnt signaling in liver cancer cells but not in colon cancer cells. However, whether and how TRIB2 regulates Wnt signaling in liver cancer cells remains unclear. Here, we report that TRIB2 negatively regulates Wnt activity through a reduction in protein stability of TCF4 and β-Catenin. Mechanistically, TRIB2 associated-ubiquitin E3 ligases beta-transducin repeat-containing E3 ubiquitin protein ligase (β-TrCP), COP1 and Smad ubiquitination regulatory factor 1 (Smurf1) reduced TCF4/β-Catenin expression, and these effects could be enhanced by TRIB2. Moreover, deletion of the binding regions of these E3-ligases within the TRIB2 protein decreased ubiquitination of TCF4/β-Catenin and reduced nuclear accumulation of β-TrCP, COP1 and Smurf1, which suggested that TRIB2 regulated-Wnt activity is closely correlated with its associated E3 ligases.Entities:
Keywords: Liver cancer; Protein stability; Ubiquitination; Wnt/β-Catenin signaling
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Year: 2014 PMID: 25311538 DOI: 10.1016/j.febslet.2014.09.042
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124