ArticlePeerJ2025
Predicting the prognosis of hepatocellular carcinoma based on genes related to polyamine metabolism.
Article in PeerJ, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Hepatocellular carcinoma (HCC) is a highly prevalent malignant tumor worldwide. Evidence showed that polyamine metabolism plays a crucial part in the regulation of cancer onset and development, however, its clinical significance in HCC remains unclear. Methods: Bulk RNA sequencing (RNA-seq) and single-cell RNA sequencing (scRNA-seq) data of HCC were collected from public databases. Polyamine metabolism-related genes (PMRGs) were obtained from the MSigDB database. The molecular subtypes of HCC were classified by ConsensusClusterPlus package, and differentially expressed genes (DEGs) of the molecular subtypes were identified by the limma package, followed by enrichment analysis with clusterProfiler package. Univariate Cox and Lasso Cox regression analyses were performed to screen core genes, construct risk model, and develop a nomogram integrating clinical characteristics for survival prediction. The obtained biomarkers were validated using Results: This study identified two molecular subtypes (C1 and C2), with C2 demonstrating a more favorable prognosis. Glucose-6-phosphate dehydrogenase ( Conclusion: In conclusion, this study screened four key genes based on PMRGs and constructed a risk model to effectively predict the prognosis of HCC, providing novel potential targets and theoretical basis for the molecular subtyping and individualized treatment of HCC.
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Registered trials
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