| Literature DB >> 29157094 |
Jia-Yin Tang1,2,3, Chen-Yang Yu1, Yu-Jie Bao1,4, Lu Chen2, Jinxian Chen2, Sheng-Li Yang3, Hao-Yan Chen3, Jie Hong3, Jing-Yuan Fang1,3.
Abstract
TEAD4 (TEA domain family member 4) was recently revealed as an oncogenic character in tumorigenesis. However, its role remains unclear in colorectal tumorigenesis. Here, we firstly found that the expression level of TEAD4 was significantly elevated in clinical samples of colorectal adenomas (CRA) and correlated with the size and histological type of CRA. Moreover, patients with higher TEAD4 expression in normal colon mucosa are more prone to be recurrent after polypectomy. TEAD4 knockdown significantly inhibited colorectal cell proliferation in vitro and suppressed tumor growth in vivo. RNA-seq and GSEA analysis reveals TEAD4 can probably regulate Hippo pathway and further experiment confirm the downstream target gene YAP1. The subsequent ChIP-qPCR and luciferase report assay indicated that TEAD4 regulated YAP1 by direct binding and transcriptional activation. In summary, our study reveals that TEAD4 plays an important tumor-promoting role in colorectal cancer by directly targeting the YAP1, thus we suggests TEAD4 may be used as a novel biomarker in colorectal tumorigenesis and provides TEAD4/YAP1 axis as a potential therapeutic option for colorectal cancer.Entities:
Keywords: Hippo pathway; TEAD4; YAP1; colorectal adenoma; transcriptional activation
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Year: 2018 PMID: 29157094 PMCID: PMC5815434 DOI: 10.1080/15384101.2017.1403687
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534