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http://purl.uniprot.org/citations/35240821http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/35240821http://www.w3.org/2000/01/rdf-schema#comment"

Objective

We aimed to explore the expression and clinical prognostic significance of PAQR4 in hepatocellular carcinoma (HCC).

Methods

We obtained the gene expression matrix and clinical data of HCC from the cancer genome atlas (TCGA) and international cancer genome consortium (ICGC) databases. The prognostic value of PAQR4 in HCC was evaluated using the Kaplan-Meier and Cox regression analyses. PAQR4-related pathways were explored by gene set enrichment analysis (GSEA). A clinical nomogram prognostic model based on the PAQR family was constructed using Cox proportional hazards models.

Results

We found that PAQR4 is overexpressed in HCC from multiple databases; additionally, quantitative real-time polymerase chain reaction (qRT-PCR) validated the upregulation of PAQR4 in HCC. PAQR4 expression was related to age, grade, alpha fetoprotein (AFP), T classification and clinical stage of HCC patients. High PAQR4 expression was associated with poor overall survival and was an independent prognostic factor for HCC patients through Kaplan-Meier analysis and Cox regression analysis, respectively. In addition, GSEA identified that the high PAQR4 expression phenotype was involved in the cell cycle, Notch signaling pathway, mTOR signaling pathway, etc. Finally, three PAQR family genes (PAQR4, PAQR8 and PAQR9) were associated with the prognosis of patients with HCC. A clinical nomogram prediction model was verified in TCGA training and ICGC validation sets, and it exerted dramatic predictive efficiency in this study.

Conclusions

PAQR4 may be regarded as a promising prognostic biomarker and therapeutic target for HCC."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.org/dc/terms/identifier"doi:10.3934/mbe.2022142"xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/author"Li Y."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/author"Li X."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/author"Yan X."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/author"Qu C."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/author"Ma T."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/name"Math Biosci Eng"xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/pages"3069-3090"xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/title"Overexpressed PAQR4 predicts poor overall survival and construction of a prognostic nomogram based on PAQR family for hepatocellular carcinoma."xsd:string
http://purl.uniprot.org/citations/35240821http://purl.uniprot.org/core/volume"19"xsd:string
http://purl.uniprot.org/citations/35240821http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/35240821
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