Supplementary Figure 2 from Reversing Effect of Ring Finger Protein 43 Inhibition on Malignant Phenotypes of human Hepatocellular Carcinoma

Xing, Chunyang; Zhou, Wuhua; Ding, Songming; Xie, Haiyang; Zhang, Wu; Yang, Zhe; Wei, Bajin; Chen, Kangjie; Su, Rong; Cheng, Jun; Zheng, Shusen; Zhou, Lin

doi:10.1158/1535-7163.22498609.v1

15357163mct120672-sup-fig2.pdf (204.28 kB)

Supplementary Figure 2 from Reversing Effect of Ring Finger Protein 43 Inhibition on Malignant Phenotypes of human Hepatocellular Carcinoma

journal contribution

posted on 2023-04-03, 13:48 authored by Chunyang Xing, Wuhua Zhou, Songming Ding, Haiyang Xie, Wu Zhang, Zhe Yang, Bajin Wei, Kangjie Chen, Rong Su, Jun Cheng, Shusen Zheng, Lin Zhou

PDF file - 204K, Effects of siRNAs on RNF43 mRNA expression. HepG2 and SMMC-7721 cells were transfected with RNF43 siRNAs (RNF43-si1, -si2, and -si3), negative control siRNAs (siNC), or Mock-transfected (Mock). RNF43 mRNA expression was measured by qRT-PCR 48 hours after transfection.

History

ARTICLE 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.