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Reversing Effect of Ring Finger Protein 43 Inhibition on Malignant Phenotypes of human Hepatocellular Carcinoma

Authors :
Lin Zhou
Wuhua Zhou
Rong Su
Chunyang Xing
Shusen Zheng
Haiyang Xie
Bajin Wei
Songming Ding
Zhe Yang
kangjchen Chen
Wu Zhang
Jun Cheng
Source :
Molecular Cancer Therapeutics. 12:94-103
Publication Year :
2013
Publisher :
American Association for Cancer Research (AACR), 2013.

Abstract

It has been shown that Ring finger protein 43 (RNF43) is overexpressed in colorectal cancer and mediates cancer cell proliferation; however, its role in hepatocellular carcinoma (HCC) remains unknown. In this study, we found that RNF43 was frequently overexpressed in HCCs, and this overexpression was correlated with positive vascular invasion, poor tumor differentiation, and advanced tumor stage. Functional studies showed that knockdown of RNF43 could induce apoptosis and inhibit proliferation, invasion, colony formation, and xenograft growth of HCCs. Microarray-based gene profiling showed a total of 229 genes differentially expressed after RNF43 knockdown, many of which are involved in oncogenic processes such as cell proliferation, cell adhesion, cell motility, cell death, DNA repair, and so on. These results suggest that RNF43 is involved in tumorigenesis and progression of HCCs and that antagonism of RNF43 may be beneficial for HCC treatment. Mol Cancer Ther; 12(1); 94–103. ©2012 AACR.

Details

ISSN :
15388514 and 15357163
Volume :
12
Database :
OpenAIRE
Journal :
Molecular Cancer Therapeutics
Accession number :
edsair.doi.dedup.....2145000b95de903124fd88d67114001f
Full Text :
https://doi.org/10.1158/1535-7163.mct-12-0672