Abstract | PURPOSE: METHODS: HCC-related data were extracted from The Cancer Genome Atlas (TCGA) database, International Cancer Genome Consortium (ICGC) database, and Gene Expression Omnibus (GEO) database. A logistic regression module was applied to analyze the relationship between the expression of COPB2 and clinicopathologic characteristics. The Cox proportional hazard regression model and Kaplan-Meier method were used for survival analysis. Gene set enrichment analysis (GSEA) was used to annotate the underlying biological functions. Loss-of-function experiments were conducted to determine the underlying mechanisms. RESULTS: COPB2 was overexpressed in HCC, and high expression of COPB2 was significantly correlated with higher alpha fetoprotein (AFP) (odds ratio (OR) = 1.616, >20 vs. ≤20, p < 0.05), stage (OR = 1.744, III vs. I, p < 0.05), and grade (OR = 1.746, G4+G3 vs. G2+G1, p < 0.05). Kaplan-Meier survival analysis showed that HCC patients with high COPB2 expression had a worse prognosis than those with low COPB2 expression (p < 0.0001 for TCGA cohort, p < 0.05 for ICGC cohort). The univariate Cox (hazard ratio (HR) = 1.068, p < 0.0001) and multivariate Cox (HR = 2.011, p < 0.05) regression analyses suggested that COPB2 was an independent risk factor. GSEA showed that mTOR and other tumor-related signaling pathways were differentially enriched in the high COPB2 expression phenotype. Silencing of COPB2 inhibited the proliferation, migration, and invasion abilities by suppressing epithelial-mesenchymal transition and mTOR signaling. CONCLUSION: COPB2 is a novel prognostic biomarker and a promising therapeutic target for HCC.
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Authors | Jiayao Zhang, Xiaoyu Wang, Guangbing Li, Jingyi He, Ziwen Lu, Yang Yang, Yong Jiang, Liyong Jiang, Feiyu Li, Jun Liu |
Journal | BioMed research international
(Biomed Res Int)
Vol. 2021
Pg. 6648078
( 2021)
ISSN: 2314-6141 [Electronic] United States |
PMID | 33824874
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 Jiayao Zhang et al. |
Chemical References |
- Biomarkers, Tumor
- COPB2 protein, human
- Coatomer Protein
- Neoplasm Proteins
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Topics |
- Biomarkers, Tumor
(genetics, metabolism)
- Carcinoma, Hepatocellular
(genetics, metabolism, mortality, pathology)
- Cell Line, Tumor
- Coatomer Protein
(genetics, metabolism)
- Disease Progression
- Disease-Free Survival
- Female
- Humans
- Liver Neoplasms
(genetics, metabolism, mortality, pathology)
- Male
- Neoplasm Proteins
(genetics, metabolism)
- Survival Rate
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