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pmid:37231356

A T-cell-related signature for prognostic stratification and immunotherapy response in hepatocellular carcinoma based on transcriptomics and single-cell sequencing.

Xu Chen · Chuang Peng · Yu Chen · Bai Ding · Sulai Liu · Yinghui Song · Yuhang Li · Bo Sun · Ranzhiqiang Yang

BMC bioinformatics · 2023 doi:10.1186/s12859-023-05344-7

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complete

Experiment

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Data

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Analysis

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title
A T-cell-related signature for prognostic stratification and immunotherapy response in hepatocellular carcinoma based on transcriptomics and single-cell sequencing.
doi
10.1186/s12859-023-05344-7
pmid
37231356
authors array · 9 items
[0]
Xu Chen
[1]
Chuang Peng
[2]
Yu Chen
[3]
Bai Ding
[4]
Sulai Liu
[5]
Yinghui Song
[6]
Yuhang Li
[7]
Bo Sun
[8]
Ranzhiqiang Yang
journal
BMC bioinformatics
year
2023
abstract
BACKGROUND: Hepatocellular carcinoma (HCC) is the fifth most frequently diagnosed malignancy and the third leading cause of cancer death globally. T cells are significantly correlated with the progression, therapy and prognosis of cancer. Limited systematic studies regarding the role of T-cell-related markers in HCC have been performed. METHODS: T-cell markers were identified with single-cell RNA sequencing (scRNA-seq) data from the GEO database. A prognostic signature was developed with the LASSO algorithm in the TCGA cohort and verified in the GSE14520 cohort. Another three eligible immunotherapy datasets, GSE91061, PRJEB25780 and IMigor210, were used to verify the role of the risk score in the immunotherapy response. RESULTS: With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively. TRPS had the highest C-index compared with the other 10 established prognostic signatures, suggesting a better performance of TRPS in predicting the prognosis of HCC. More importantly, the TRPS risk score was closely correlated with the TIDE score and immunophenoscore. The high-risk score patients had a higher percentage of SD/PD, and CR/PR occurred more frequently in patients with low TRPS-related risk scores in the IMigor210, PRJEB25780 and GSE91061 cohorts. We also constructed a nomogram based on the TRPS, which had high potential for clinical application. CONCLUSION: Our study proposed a novel TRPS for HCC patients, and the TRPS could effectively indicate the prognosis of HCC. It also served as a predictor for immunotherapy.
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After performing LASSO regression analysis, a total of 13 T-cell-related genes were selected for the prognostic signature, and the coefficient of the candidate gene is shown in Additional file 6: Figure S3A-3B.
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sections[13] "Construction and validation of the T-cell-related prognostic signature (TRPS) for HCC" paragraph 2
quote
After performing LASSO regression analysis, a total of 13 T-cell-related genes were selected for the prognostic signature, and the coefficient of the candidate gene is shown in Additional file 6: Figure S3A-3B.
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sections[26] "notes" paragraph 1
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The analyzed datasets generated during the study are available from the corresponding author on reasonable request.
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With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively.
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sections[0] "Abstract" paragraph 3
quote
With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively.
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With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively.
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3921;571
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title
Gene expression data of human hepatocellular carcinoma (HCC)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[2] object · 15 fields
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data:geo:GSE162616
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The analyzed datasets generated during the study are available from the corresponding author on reasonable request.
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null
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24676
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Homo sapiens
title
Single-Cell Transcriptomic Atlas of Human Hepatic ILCs Reveals the Enrichment of ILC2 in Liver Cancer
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[3] object · 15 fields
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data:geo:GSE91061
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null
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The analyzed datasets generated during the study are available from the corresponding author on reasonable request.
structure object · 15 fields
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109
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null
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9052
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Homo sapiens
title
Molecular portraits of tumor mutational and micro-environmental sculpting by immune checkpoint blockade therapy
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[4] object · 15 fields
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identifier_resolution_only_no_download_no_licence_read
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After performing LASSO regression analysis, a total of 13 T-cell-related genes were selected for the prognostic signature, and the coefficient of the candidate gene is shown in Additional file 6: Figure S3A-3B.
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[0]
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[0]
esponse in hepatocellular carcinoma based on transcriptomics and single-cell sequencing.
[1]
ell markers were identified with single-cell RNA sequencing (scRNA-seq) data from the GEO database. A pr
order_basis
paper_text_order:76
id
assay:1
[1] object · 11 fields
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[0]
METHODS: T-cell markers were identified with single-cell RNA sequencing (scRNA-seq) data from the GEO database. A pr
[1]
identified with single-cell RNA sequencing (scRNA-seq) data from the GEO database. A prognostic si
[2]
SULTS: With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based pro
order_basis
paper_text_order:504
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37231356", "kind": "science-record", "revision": 2, "content_hash": "sha256:69ccf668a51bf02eaea69f0b72a95ba039cf8aeae628609fa06a8e7574427c8f", "created_at": "2026-11-01T19:01:56Z", "updated_at": "2026-11-01T21:30:51Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A T-cell-related signature for prognostic stratification and immunotherapy response in hepatocellular carcinoma based on transcriptomics and single-cell sequencing.", "doi": "10.1186/s12859-023-05344-7", "pmid": "37231356", "authors": ["Xu Chen", "Chuang Peng", "Yu Chen", "Bai Ding", "Sulai Liu", "Yinghui Song", "Yuhang Li", "Bo Sun", "Ranzhiqiang Yang"], "journal": "BMC bioinformatics", "year": 2023, "abstract": "BACKGROUND: Hepatocellular carcinoma (HCC) is the fifth most frequently diagnosed malignancy and the third leading cause of cancer death globally. T cells are significantly correlated with the progression, therapy and prognosis of cancer. Limited systematic studies regarding the role of T-cell-related markers in HCC have been performed.\nMETHODS: T-cell markers were identified with single-cell RNA sequencing (scRNA-seq) data from the GEO database. A prognostic signature was developed with the LASSO algorithm in the TCGA cohort and verified in the GSE14520 cohort. Another three eligible immunotherapy datasets, GSE91061, PRJEB25780 and IMigor210, were used to verify the role of the risk score in the immunotherapy response.\nRESULTS: With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively. TRPS had the highest C-index compared with the other 10 established prognostic signatures, suggesting a better performance of TRPS in predicting the prognosis of HCC. More importantly, the TRPS risk score was closely correlated with the TIDE score and immunophenoscore. The high-risk score patients had a higher percentage of SD/PD, and CR/PR occurred more frequently in patients with low TRPS-related risk scores in the IMigor210, PRJEB25780 and GSE91061 cohorts. We also constructed a nomogram based on the TRPS, which had high potential for clinical application.\nCONCLUSION: Our study proposed a novel TRPS for HCC patients, and the TRPS could effectively indicate the prognosis of HCC. It also served as a predictor for immunotherapy.", "claims": [{"id": "claim-method", "statement": "After performing LASSO regression analysis, a total of 13 T-cell-related genes were selected for the prognostic signature, and the coefficient of the candidate gene is shown in Additional file 6: Figure S3A-3B.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37231356", "locator": "sections[13] \"Construction and validation of the T-cell-related prognostic signature (TRPS) for HCC\" paragraph 2", "quote": "After performing LASSO regression analysis, a total of 13 T-cell-related genes were selected for the prognostic signature, and the coefficient of the candidate gene is shown in Additional file 6: Figure S3A-3B."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The analyzed datasets generated during the study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37231356", "locator": "sections[26] \"notes\" paragraph 1", "quote": "The analyzed datasets generated during the study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37231356", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "With 181 T-cell markers identified by scRNA-seq analysis, a 13 T-cell-related gene-based prognostic signature (TRPS) was developed for prognostic prediction, which divided HCC patients into high-risk and low-risk groups according to overall survival, with AUCs of 1 year, 3 years, and 5 years of 0.807, 0.752, and 0.708, respectively.", "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:37231356"], "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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