| Literature DB >> 25434796 |
Kailiang Zhang1, Shanjun Zhu1, Yanwei Liu2, Xiaoqun Dong3, Zhendong Shi1, Anling Zhang1, Chaoyong Liu4, Luyue Chen1, Jianwei Wei1, Peiyu Pu1, Jianning Zhang1, Tao Jiang5, Lei Han6, Chunsheng Kang7.
Abstract
Inhibitor of β-catenin and T-cell factor (ICAT) is a key component of Wnt/β-catenin signaling. ICAT blocks the formation of the β-catenin/TCF complex and has been demonstrated to be involved in embryonic development and carcinogenesis. As an inhibitor of canonical Wnt signaling, ICAT was presumed to be a tumor-suppressor gene. However, the ICAT functions in human glioma remain unknown. In this study, we evaluated the expression of ICAT in 305 human glioma tissues and found that negative ICAT expression correlated with higher grade glioma and poor survival in patients with glioma. Then we transfected glioma cells with ICAT plasmid. Western blotting showed an increased ICAT protein expression level in glioma cells. MTT assay, flow cytometry and cell invasion assay were used to detect cell proliferation, cell cycle distribution, apoptosis and invasion. Our studies confirmed that ICAT inhibits glioma cell proliferation and invasion, and it induces cell apoptosis and cell cycle progression arrest. Besides, ICAT slowed down tumor growth in a glioblastoma xenograft model. Therefore, our study demonstrates that ICAT may serve as a tumor-suppressor in human glioma suggesting a promising direction for targeting therapy in glioma.Entities:
Keywords: Glioma; ICAT; Proliferation; Wnt; β-catenin
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Year: 2014 PMID: 25434796 DOI: 10.1016/j.canlet.2014.11.047
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679