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pmid:32337237
The Oncogenic Role of CENPA in Hepatocellular Carcinoma Development: Evidence from Bioinformatic Analysis.
Yuan Zhang · Lei Yang · Jia Shi · Yunfei Lu · Xiaorong Chen · Zongguo Yang
BioMed research international · 2020 doi:10.1155/2020/3040839
Paper
complete
Experiment
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Data
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Analysis
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Execution
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Complete file
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A Cox regression hazard model was also performed.\nRESULTS: CENPA mRNA was significantly upregulated in tumor tissues compared with that in adjacent tissues, which were validated in The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) series (all P < 0.01). In the Kaplan-Meier plotter platform, the high level of CENPA mRNA was significantly correlated with overall survival (OS), disease-free survival (DFS), recurrence-free survival (RFS), and progression-free survival (PFS) in HCC patients (all log rank P < 0.01). For validation in GSE14520 and pan-TCGA dataset, HCC patients with CNEPA mRNA overexpression had poor OS compared with those with low CENPA mRNA (log rank P = 0.025 and P < 0.0001, respectively), and those with high CENPA had poor DFS in TCGA (log rank P = 0.0001). Additionally, CENPA mRNA were upregulated in HCC patients with alpha-fetoprotein (AFP) elevation, advanced TNM stage, larger tumor size, advanced AJCC stage, advanced pathology grade, and vascular invasion (all P < 0.05). A Cox regression model including CENPA, OIP5, and AURKB could predict OS in HCC patients effectively (AUC = 0.683).\nCONCLUSION: Overexpressed in tumors, CENPA might be an oncogenic factor in the development of HCC patients.", "claims": [{"id": "claim-method", "statement": "Two patient groups were compared by the Kaplan-Meier survival plot and the hazard ratio (HR) with 95% confidence intervals (CI), and log rank P value was calculated.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32337237", "locator": "sections[4] \"2.2. 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