| Literature DB >> 26230915 |
Hao Weng1, Xu'an Wang1, Maolan Li1, Xiangsong Wu1, Zheng Wang1, Wenguang Wu1, Zhou Zhang1, Yijian Zhang1, Shuai Zhao1, Shibo Liu1, Jiasheng Mu1, Yang Cao1, Yijun Shu1, Runfa Bao1, Jian Zhou1, Jianhua Lu1, Ping Dong1, Jun Gu1, Yingbin Liu1.
Abstract
The Zinc finger X-chromosomal protein (ZFX), a novel member of the Krueppel C2H2-type zinc finger protein family, has been implicated in multiple human cancers. However, the clinical significance of ZFX expression in gallbladder cancer (GBC) remains largely unknown. In this study, we focused on the clinical significance, biological function and mechanism of ZFX in GBC, and found that ZFX protein overexpression was frequently detected in GBC tissues. The expression of ZFX was significantly correlated with histological grade, perineural invasion, and margin status and lead to a significantly poorer prognosis in GBC patients(P <0.001). Furthermore, knockdown of ZFX result in significant inhibition of proliferation, migration, invasion and cause cell cycle arrest in GBC-SD cells, while over-expression of ZFX in NOZ shows the opposite results. Activation of PI3K/AKT pathway maybe the potential mechanism behind these effects. In conclusion, ZFX may serve as a oncogene and could be used as a potential prognostic marker and genetic treatment target for GBC patients.Entities:
Keywords: Gallbladder cancer; Immunohistochemistry; PI3K/AKT pathway; RNA interference; Zinc finger X-chromosomal protein; cell cycle regulation; proliferation
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Year: 2015 PMID: 26230915 PMCID: PMC4846125 DOI: 10.1080/15384047.2015.1070994
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742