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pmid:33402113

A gene-based risk score model for predicting recurrence-free survival in patients with hepatocellular carcinoma.

Wenhua Wang · Lingchen Wang · Xinsheng Xie · Yehong Yan · Yue Li · Quqin Lu

BMC cancer · 2021 doi:10.1186/s12885-020-07692-6

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pmid:33402113
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title
A gene-based risk score model for predicting recurrence-free survival in patients with hepatocellular carcinoma.
doi
10.1186/s12885-020-07692-6
pmid
33402113
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Wenhua Wang
[1]
Lingchen Wang
[2]
Xinsheng Xie
[3]
Yehong Yan
[4]
Yue Li
[5]
Quqin Lu
journal
BMC cancer
year
2021
abstract
BACKGROUND: Hepatocellular carcinoma (HCC) remains the most frequent liver cancer, accounting for approximately 90% of primary liver cancers worldwide. The recurrence-free survival (RFS) of HCC patients is a critical factor in devising a personal treatment plan. Thus, it is necessary to accurately forecast the prognosis of HCC patients in clinical practice. METHODS: Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. Then, the GSE76427 dataset was used to evaluate the prognostic model's effectiveness. RESULTS: We identified 1331 differentially expressed genes associated with RFS. Seven of these genes were selected to generate the prognostic model. The validation in both the TCGA cohort and GEO cohort demonstrated that the 7-gene prognostic model can predict the RFS of HCC patients. Meanwhile, the results of the multivariate Cox regression analysis showed that the 7-gene risk score model could function as an independent prognostic factor. In addition, according to the time-dependent ROC curve, the 7-gene risk score model performed better in predicting the RFS of the training set and the external validation dataset than the classical TNM staging and BCLC. Furthermore, these seven genes were found to be related to the occurrence and development of liver cancer by exploring three other databases. CONCLUSION: Our study identified a seven-gene signature for HCC RFS prediction that can be used as a novel and convenient prognostic tool. These seven genes might be potential target genes for metabolic therapy and the treatment of HCC.
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Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. Then, the GSE76427 dataset was used to evaluate the prognostic model’s effectiveness.
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Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. Then, the GSE76427 dataset was used to evaluate the prognostic model’s effectiveness.
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The gene expression profiles and clinical information datasets downloaded from The Cancer Genome Atlas (TCGA-LIHC)(https://portal.gdc.cancer.gov) and the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov), accession numbers: GSE76427. Genetic alterations was retrieved from the cBioPortal website (http://www.cbioportal.org/).
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The gene expression profiles and clinical information datasets downloaded from The Cancer Genome Atlas (TCGA-LIHC)(https://portal.gdc.cancer.gov) and the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov), accession numbers: GSE76427. Genetic alterations was retrieved from the cBioPortal website (http://www.cbioportal.org/).
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The best genes predicting recurrence-free survival of hepatocellular carcinoma patients
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Characteristics of HCC patients in TCGA-LIHC dataset
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Characteristics of HCC patients in GSE 76427 dataset
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Univariate and multivariate Cox regression in TCGA-LIHC hepatectomized patients
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Independent prognostic role of the prognostic gene signature
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Univariate and multivariate Cox regression in TCGA-LIHC hepatectomized patients
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Comparison of the prognostic model with the TNM and BCLC model
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Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. Then, the GSE76427 dataset was used to evaluate the prognostic model’s effectiveness.
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The gene expression profiles and clinical information datasets downloaded from The Cancer Genome Atlas (TCGA-LIHC)(https://portal.gdc.cancer.gov) and the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov), accession numbers: GSE76427. Genetic alterations was retrieved from the cBioPortal website (http://www.cbioportal.org/).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33402113", "kind": "science-record", "revision": 7, "content_hash": "sha256:ecd3d8349ba90471b0e9283d97fae6eb54601dd121a3a0efb211a49cc999fa6c", "created_at": "2026-11-01T15:41:21Z", "updated_at": "2026-11-01T22:02:52Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A gene-based risk score model for predicting recurrence-free survival in patients with hepatocellular carcinoma.", "doi": "10.1186/s12885-020-07692-6", "pmid": "33402113", "authors": ["Wenhua Wang", "Lingchen Wang", "Xinsheng Xie", "Yehong Yan", "Yue Li", "Quqin Lu"], "journal": "BMC cancer", "year": 2021, "abstract": "BACKGROUND: Hepatocellular carcinoma (HCC) remains the most frequent liver cancer, accounting for approximately 90% of primary liver cancers worldwide. The recurrence-free survival (RFS) of HCC patients is a critical factor in devising a personal treatment plan. Thus, it is necessary to accurately forecast the prognosis of HCC patients in clinical practice.\nMETHODS: Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. Then, the GSE76427 dataset was used to evaluate the prognostic model's effectiveness.\nRESULTS: We identified 1331 differentially expressed genes associated with RFS. Seven of these genes were selected to generate the prognostic model. The validation in both the TCGA cohort and GEO cohort demonstrated that the 7-gene prognostic model can predict the RFS of HCC patients. Meanwhile, the results of the multivariate Cox regression analysis showed that the 7-gene risk score model could function as an independent prognostic factor. In addition, according to the time-dependent ROC curve, the 7-gene risk score model performed better in predicting the RFS of the training set and the external validation dataset than the classical TNM staging and BCLC. Furthermore, these seven genes were found to be related to the occurrence and development of liver cancer by exploring three other databases.\nCONCLUSION: Our study identified a seven-gene signature for HCC RFS prediction that can be used as a novel and convenient prognostic tool. These seven genes might be potential target genes for metabolic therapy and the treatment of HCC.", "claims": [{"id": "claim-method", "statement": "Using The Cancer Genome Atlas (TCGA) dataset, we identified genes associated with RFS. A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. 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A robust likelihood-based survival modeling approach was used to select the best genes for the prognostic model. 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