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pmid:33962640

A prognostic model based on seven immune-related genes predicts the overall survival of patients with hepatocellular carcinoma.

Qian Yan · Wenjiang Zheng · Boqing Wang · Baoqian Ye · Huiyan Luo · Xinqian Yang · Ping Zhang · Xiongwen Wang

BioData mining · 2021 doi:10.1186/s13040-021-00261-y

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title
A prognostic model based on seven immune-related genes predicts the overall survival of patients with hepatocellular carcinoma.
doi
10.1186/s13040-021-00261-y
pmid
33962640
authors array · 8 items
[0]
Qian Yan
[1]
Wenjiang Zheng
[2]
Boqing Wang
[3]
Baoqian Ye
[4]
Huiyan Luo
[5]
Xinqian Yang
[6]
Ping Zhang
[7]
Xiongwen Wang
journal
BioData mining
year
2021
abstract
BACKGROUND: Hepatocellular carcinoma (HCC) is a disease with a high incidence and a poor prognosis. Growing amounts of evidence have shown that the immune system plays a critical role in the biological processes of HCC such as progression, recurrence, and metastasis, and some have discussed using it as a weapon against a variety of cancers. However, the impact of immune-related genes (IRGs) on the prognosis of HCC remains unclear. METHODS: Based on The Cancer Gene Atlas (TCGA) and Immunology Database and Analysis Portal (ImmPort) datasets, we integrated the ribonucleic acid (RNA) sequencing profiles of 424 HCC patients with IRGs to calculate immune-related differentially expressed genes (DEGs). Survival analysis was used to establish a prognostic model of survival- and immune-related DEGs. Based on genomic and clinicopathological data, we constructed a nomogram to predict the prognosis of HCC patients. Gene set enrichment analysis further clarified the signalling pathways of the high-risk and low-risk groups constructed based on the IRGs in HCC. Next, we evaluated the correlation between the risk score and the infiltration of immune cells, and finally, we validated the prognostic performance of this model in the GSE14520 dataset. RESULTS: A total of 100 immune-related DEGs were significantly associated with the clinical outcomes of patients with HCC. We performed univariate and multivariate least absolute shrinkage and selection operator (Lasso) regression analyses on these genes to construct a prognostic model of seven IRGs (Fatty Acid Binding Protein 6 (FABP6), Microtubule-Associated Protein Tau (MAPT), Baculoviral IAP Repeat Containing 5 (BIRC5), Plexin-A1 (PLXNA1), Secreted Phosphoprotein 1 (SPP1), Stanniocalcin 2 (STC2) and Chondroitin Sulfate Proteoglycan 5 (CSPG5)), which showed better prognostic performance than the tumour/node/metastasis (TNM) staging system. Moreover, we constructed a regulatory network related to transcription factors (TFs) that further unravelled the regulatory mechanisms of these genes. According to the median value of the risk score, the entire TCGA cohort was divided into high-risk and low-risk groups, and the low-risk group had a better overall survival (OS) rate. To predict the OS rate of HCC, we established a gene- and clinical factor-related nomogram. The receiver operating characteristic (ROC) curve, concordance index (C-index) and calibration curve showed that this model had moderate accuracy. The correlation analysis between the risk score and the infiltration of six common types of immune cells showed that the model could reflect the state of the immune microenvironment in HCC tumours. CONCLUSION: Our IRG prognostic model was shown to have value in the monitoring, treatment, and prognostic assessment of HCC patients and could be used as a survival prediction tool in the near future.
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Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells.
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sections[11] "Relationship between risk sore and immune cell infiltration" paragraph 2
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Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells.
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The datasets for this study can be found in TCGA [https://portal.gdc.cancer.gov/] and GEO databases [https://www.ncbi.nlm.nih.gov/geo/].
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The datasets for this study can be found in TCGA [https://portal.gdc.cancer.gov/] and GEO databases [https://www.ncbi.nlm.nih.gov/geo/].
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Gene expression data of human hepatocellular carcinoma (HCC)
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Clinical information in training and validation groups
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Screening of prognosis-specific IRGs
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Table 1
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Clinical information in training and validation groups
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high
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47
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The relationship between clinical factors and risk scores or the expression of seven prognostic related immune genes in hepatocellular carcinoma
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section_index
21
section_title
The correlation between clinical factors and gene signature in IPM
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Table 2
caption
The relationship between clinical factors and risk scores or the expression of seven prognostic related immune genes in hepatocellular carcinoma
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N
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11.791 (4.946e-14)
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−1.121 (0.374)
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−2.198 (0.030)
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−1.288 (0.201)
[5]
− 1.383 (0.170)
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2.511 (0.055)
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Risk Score
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section[21]/table-wrap[1]#Tab2
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Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells.
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Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33962640", "kind": "science-record", "revision": 7, "content_hash": "sha256:ff5483bc280b8e05b57a93a6ccf84a4fe9ab29b7d8f6d378688b6fec6dbc4652", "created_at": "2026-11-01T15:41:34Z", "updated_at": "2026-11-01T22:03:42Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A prognostic model based on seven immune-related genes predicts the overall survival of patients with hepatocellular carcinoma.", "doi": "10.1186/s13040-021-00261-y", "pmid": "33962640", "authors": ["Qian Yan", "Wenjiang Zheng", "Boqing Wang", "Baoqian Ye", "Huiyan Luo", "Xinqian Yang", "Ping Zhang", "Xiongwen Wang"], "journal": "BioData mining", "year": 2021, "abstract": "BACKGROUND: Hepatocellular carcinoma (HCC) is a disease with a high incidence and a poor prognosis. Growing amounts of evidence have shown that the immune system plays a critical role in the biological processes of HCC such as progression, recurrence, and metastasis, and some have discussed using it as a weapon against a variety of cancers. However, the impact of immune-related genes (IRGs) on the prognosis of HCC remains unclear.\nMETHODS: Based on The Cancer Gene Atlas (TCGA) and Immunology Database and Analysis Portal (ImmPort) datasets, we integrated the ribonucleic acid (RNA) sequencing profiles of 424 HCC patients with IRGs to calculate immune-related differentially expressed genes (DEGs). Survival analysis was used to establish a prognostic model of survival- and immune-related DEGs. Based on genomic and clinicopathological data, we constructed a nomogram to predict the prognosis of HCC patients. Gene set enrichment analysis further clarified the signalling pathways of the high-risk and low-risk groups constructed based on the IRGs in HCC. Next, we evaluated the correlation between the risk score and the infiltration of immune cells, and finally, we validated the prognostic performance of this model in the GSE14520 dataset.\nRESULTS: A total of 100 immune-related DEGs were significantly associated with the clinical outcomes of patients with HCC. We performed univariate and multivariate least absolute shrinkage and selection operator (Lasso) regression analyses on these genes to construct a prognostic model of seven IRGs (Fatty Acid Binding Protein 6 (FABP6), Microtubule-Associated Protein Tau (MAPT), Baculoviral IAP Repeat Containing 5 (BIRC5), Plexin-A1 (PLXNA1), Secreted Phosphoprotein 1 (SPP1), Stanniocalcin 2 (STC2) and Chondroitin Sulfate Proteoglycan 5 (CSPG5)), which showed better prognostic performance than the tumour/node/metastasis (TNM) staging system. Moreover, we constructed a regulatory network related to transcription factors (TFs) that further unravelled the regulatory mechanisms of these genes. According to the median value of the risk score, the entire TCGA cohort was divided into high-risk and low-risk groups, and the low-risk group had a better overall survival (OS) rate. To predict the OS rate of HCC, we established a gene- and clinical factor-related nomogram. The receiver operating characteristic (ROC) curve, concordance index (C-index) and calibration curve showed that this model had moderate accuracy. The correlation analysis between the risk score and the infiltration of six common types of immune cells showed that the model could reflect the state of the immune microenvironment in HCC tumours.\nCONCLUSION: Our IRG prognostic model was shown to have value in the monitoring, treatment, and prognostic assessment of HCC patients and could be used as a survival prediction tool in the near future.", "claims": [{"id": "claim-method", "statement": "Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33962640", "locator": "sections[11] \"Relationship between risk sore and immune cell infiltration\" paragraph 2", "quote": "Hence, we performed Pearson correlation analysis between risk score and the content of six types of immune cells."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets for this study can be found in TCGA [https://portal.gdc.cancer.gov/] and GEO databases [https://www.ncbi.nlm.nih.gov/geo/].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33962640", "locator": "sections[29] \"Availability of data and materials\" paragraph 2", "quote": "The datasets for this study can be found in TCGA [https://portal.gdc.cancer.gov/] and GEO databases [https://www.ncbi.nlm.nih.gov/geo/]."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:33962640"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE14520"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE14520"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:33962640", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s13040-021-00261-y", "sha256": 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