| Literature DB >> 24532795 |
Xuehe Xu1, Tianxin Yu, Jiandang Shi, Xi Chen, Wen Zhang, Ting Lin, Zhihong Liu, Yadong Wang, Zheng Zeng, Chi Wang, Mingsong Li, Chunming Liu.
Abstract
Wnt signaling plays an important role in colorectal cancer (CRC). Although the mechanisms of β-catenin degradation have been well studied, the mechanism by which β-catenin activates transcription is still not fully understood. While screening a panel of DNA demethylases, we found that thymine DNA glycosylase (TDG) up-regulated Wnt signaling. TDG interacts with the transcription factor TCF4 and coactivator CREB-binding protein/p300 in the Wnt pathway. Knocking down TDG by shRNAs inhibited the proliferation of CRC cells in vitro and in vivo. In CRC patients, TDG levels were significantly higher in tumor tissues than in the adjacent normal tissues. These results suggest that TDG warrants consideration as a potential biomarker for CRC and as a target for CRC treatment.Entities:
Keywords: Cell Growth; Colorectal Cancer; Protein-Protein Interactions; Transcription Coactivators; Wnt Signaling
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Year: 2014 PMID: 24532795 PMCID: PMC3979391 DOI: 10.1074/jbc.M113.538835
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157