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Reversing Effect of Ring Finger Protein 43 Inhibition on Malignant Phenotypes of human Hepatocellular Carcinoma
- 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.
- Subjects :
- Adult
Male
Cancer Research
Programmed cell death
Carcinoma, Hepatocellular
Cell Survival
DNA repair
Ubiquitin-Protein Ligases
Mice, Nude
Biology
medicine.disease_cause
Mice
Young Adult
Cell Movement
Cell Line, Tumor
Cell Adhesion
medicine
Carcinoma
Animals
Humans
RNA, Small Interfering
Cell adhesion
Aged
Cell Proliferation
Oncogene Proteins
Mice, Inbred BALB C
Gene knockdown
Cell growth
Liver Neoplasms
Middle Aged
medicine.disease
Molecular biology
Matrix Metalloproteinases
digestive system diseases
Extracellular Matrix
Tumor Burden
DNA-Binding Proteins
Cell Transformation, Neoplastic
Phenotype
Oncology
Apoptosis
Gene Knockdown Techniques
Cancer research
Female
Transcriptome
Carcinogenesis
Neoplasm Transplantation
Subjects
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