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ICAT inhibits glioblastoma cell proliferation by suppressing Wnt/β-catenin activity.

Authors :
Zhang, Kailiang
Zhu, Shanjun
Liu, Yanwei
Dong, Xiaoqun
Shi, Zhendong
Zhang, Anling
Liu, Chaoyong
Chen, Luyue
Wei, Jianwei
Pu, Peiyu
Zhang, Jianning
Jiang, Tao
Han, Lei
Kang, Chunsheng
Source :
Cancer Letters. Feb2015, Vol. 357 Issue 1, p404-411. 8p.
Publication Year :
2015

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03043835
Volume :
357
Issue :
1
Database :
Academic Search Index
Journal :
Cancer Letters
Publication Type :
Academic Journal
Accession number :
100152684
Full Text :
https://doi.org/10.1016/j.canlet.2014.11.047