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pmid:36311759

Analysis on heterogeneity of hepatocellular carcinoma immune cells and a molecular risk model by integration of scRNA-seq and bulk RNA-seq.

Xiaorui Liu · Jingjing Li · Qingxiang Wang · Lu Bai · Jiyuan Xing · Xiaobo Hu · Shuang Li · Qinggang Li

Frontiers in immunology · 2022 doi:10.3389/fimmu.2022.1012303

Paper

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Experiment

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Data

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pmid:36311759
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2026-11-01T18:15:43Z
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title
Analysis on heterogeneity of hepatocellular carcinoma immune cells and a molecular risk model by integration of scRNA-seq and bulk RNA-seq.
doi
10.3389/fimmu.2022.1012303
pmid
36311759
authors array · 8 items
[0]
Xiaorui Liu
[1]
Jingjing Li
[2]
Qingxiang Wang
[3]
Lu Bai
[4]
Jiyuan Xing
[5]
Xiaobo Hu
[6]
Shuang Li
[7]
Qinggang Li
journal
Frontiers in immunology
year
2022
abstract
Background: Studies have shown that hepatocellular carcinoma (HCC) heterogeneity is a main cause leading to failure of treatment. Technology of single-cell sequencing (scRNA) could more accurately reveal the essential characteristics of tumor genetics. Methods: From the Gene Expression Omnibus (GEO) database, HCC scRNA-seq data were extracted. The FindCluster function was applied to analyze cell clusters. Autophagy-related genes were acquired from the MSigDB database. The ConsensusClusterPlus package was used to identify molecular subtypes. A prognostic risk model was built with the Least Absolute Shrinkage and Selection Operator (LASSO)-Cox algorithm. A nomogram including a prognostic risk model and multiple clinicopathological factors was constructed. Results: Eleven cell clusters labeled as various cell types by immune cell markers were obtained from the combined scRNA-seq GSE149614 dataset. ssGSEA revealed that autophagy-related pathways were more enriched in malignant tumors. Two autophagy-related clusters (C1 and C2) were identified, in which C1 predicted a better survival, enhanced immune infiltration, and a higher immunotherapy response. LASSO-Cox regression established an eight-gene signature. Next, the HCCDB18, GSA14520, and GSE76427 datasets confirmed a strong risk prediction ability of the signature. Moreover, the low-risk group had enhanced immune infiltration and higher immunotherapy response. A nomogram which consisted of RiskScore and clinical features had better prediction ability. Conclusion: To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.
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LASSO–Cox regression was conducted in the glmnet package in R language to select prognostic genes (21).
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sections[9] "Construction and evaluation of a prognostic risk model for HCC" paragraph 2
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LASSO–Cox regression was conducted in the glmnet package in R language to select prognostic genes (21).
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sections[26] "Data availability statement" paragraph 2
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
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To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.
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sections[0] "Abstract" paragraph 4
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To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.
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To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.
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https://doi.org/10.3389/fimmu.2022.1012303
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Homo sapiens
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Gene expression data of human hepatocellular carcinoma (HCC)
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
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null
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24676
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Homo sapiens
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A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
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10558
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Homo sapiens
title
Microarray expression data for tumor and adjacent non-tumor tissues from hepatocellular carcinoma patients
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2026-11-01T15:39:55Z
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and a molecular risk model by integration of scRNA-seq and bulk RNA-seq.
[1]
Gene Expression Omnibus (GEO) database, HCC scRNA-seq data were extracted. The FindCluster functio
[2]
cell markers were obtained from the combined scRNA-seq GSE149614 dataset. ssGSEA revealed that auto
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k model by integration of scRNA-seq and bulk RNA-seq.
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LASSO–Cox regression was conducted in the glmnet package in R language to select prognostic genes (21).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36311759", "kind": "science-record", "revision": 3, "content_hash": "sha256:cf7f3f9a3769f8d8d113212e14d6bb7260f18c49fcd98cf4831bde1fb07c89e6", "created_at": "2026-11-01T18:15:43Z", "updated_at": "2026-11-01T21:29:21Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Analysis on heterogeneity of hepatocellular carcinoma immune cells and a molecular risk model by integration of scRNA-seq and bulk RNA-seq.", "doi": "10.3389/fimmu.2022.1012303", "pmid": "36311759", "authors": ["Xiaorui Liu", "Jingjing Li", "Qingxiang Wang", "Lu Bai", "Jiyuan Xing", "Xiaobo Hu", "Shuang Li", "Qinggang Li"], "journal": "Frontiers in immunology", "year": 2022, "abstract": "Background: Studies have shown that hepatocellular carcinoma (HCC) heterogeneity is a main cause leading to failure of treatment. Technology of single-cell sequencing (scRNA) could more accurately reveal the essential characteristics of tumor genetics.\nMethods: From the Gene Expression Omnibus (GEO) database, HCC scRNA-seq data were extracted. The FindCluster function was applied to analyze cell clusters. Autophagy-related genes were acquired from the MSigDB database. The ConsensusClusterPlus package was used to identify molecular subtypes. A prognostic risk model was built with the Least Absolute Shrinkage and Selection Operator (LASSO)-Cox algorithm. A nomogram including a prognostic risk model and multiple clinicopathological factors was constructed.\nResults: Eleven cell clusters labeled as various cell types by immune cell markers were obtained from the combined scRNA-seq GSE149614 dataset. ssGSEA revealed that autophagy-related pathways were more enriched in malignant tumors. Two autophagy-related clusters (C1 and C2) were identified, in which C1 predicted a better survival, enhanced immune infiltration, and a higher immunotherapy response. LASSO-Cox regression established an eight-gene signature. Next, the HCCDB18, GSA14520, and GSE76427 datasets confirmed a strong risk prediction ability of the signature. Moreover, the low-risk group had enhanced immune infiltration and higher immunotherapy response. A nomogram which consisted of RiskScore and clinical features had better prediction ability.\nConclusion: To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.", "claims": [{"id": "claim-method", "statement": "LASSO–Cox regression was conducted in the glmnet package in R language to select prognostic genes (21).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36311759", "locator": "sections[9] \"Construction and evaluation of a prognostic risk model for HCC\" paragraph 2", "quote": "LASSO–Cox regression was conducted in the glmnet package in R language to select prognostic genes (21)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36311759", "locator": "sections[26] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36311759", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "To precisely assess the prognostic risk, an eight-gene prognostic stratification signature was developed based on the heterogeneity of HCC immune cells.", "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:36311759"], "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. 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