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pmid:36341357

A CD8+ T cell-associated immune gene panel for prediction of the prognosis and immunotherapeutic effect of melanoma.

Shanwen Sun · Zhengke Zhi · Yang Su · Jingxian Sun · Qianjun Li

Frontiers in immunology · 2022 doi:10.3389/fimmu.2022.1039565

Paper

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Experiment

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Data

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title
A CD8+ T cell-associated immune gene panel for prediction of the prognosis and immunotherapeutic effect of melanoma.
doi
10.3389/fimmu.2022.1039565
pmid
36341357
authors array · 5 items
[0]
Shanwen Sun
[1]
Zhengke Zhi
[2]
Yang Su
[3]
Jingxian Sun
[4]
Qianjun Li
journal
Frontiers in immunology
year
2022
abstract
Background: Skin cutaneous melanoma (SKCM) is the most frequently encountered tumor of the skin. Immunotherapy has opened a new horizon in melanoma treatment. We aimed to construct a CD8+ T cell-associated immune gene prognostic model (CDIGPM) for SKCM and unravel the immunologic features and the benefits of immunotherapy in CDIGPM-defined SKCM groups. Method: Single-cell SKCM transcriptomes were utilized in conjunction with immune genes for the screening of CD8+ T cell-associated immune genes (CDIGs) for succeeding assessment. Thereafter, through protein-protein interaction (PPI) networks analysis, univariate COX analysis, and multivariate Cox analysis, six genes (MX1, RSAD2, IRF2, GBP2, IFITM1, and OAS2) were identified to construct a CDIGPM. We detected cell proliferation of SKCM cells transfected with IRF2 siRNA. Then, we analyzed the immunologic features and the benefits of immunotherapy in CDIGPM-defined groups. Results: The overall survival (OS) was much better in low-CDIGPM group versus high CDIGPM group in TCGA dataset and GSE65904 dataset. On the whole, the results unfolded that a low CDIGPM showed relevance to immune response-correlated pathways, high expressions of CTLA4 and PD-L1, a high infiltration rate of CD8+ T cells, and more benefits from immunotherapy. Conclusion: CDIGPM is an good model to predict the prognosis, the potential immune escape from immunotherapy for SKCM, and define immunologic and molecular features.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575.
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The low-CDIGPM group showed better overall survival, enrichment of immune-response-related pathways, higher CTLA4 and PD-L1 expression, greater CD8+ T-cell infiltration, and greater benefit from immunotherapy.
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The overall survival (OS) was much better in low-CDIGPM group versus high CDIGPM group in TCGA dataset and GSE65904 dataset.
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On the whole, the results unfolded that a low CDIGPM showed relevance to immune response-correlated pathways, high expressions of CTLA4 and PD-L1, a high infiltration rate of CD8+ T cells, and more benefits from immunotherapy.
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The low-CDIGPM group showed better overall survival, enrichment of immune-response-related pathways, higher CTLA4 and PD-L1 expression, greater CD8+ T-cell infiltration, and greater benefit from immunotherapy.
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data_shapes array · 1 item
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evidence object · 3 fields
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0.8
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χ2
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complete
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Automated Assays Laravel application and simulated adapters
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survival_km
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
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GSE35640
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GSE35640
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575.
basis
The paper names GSE120575, GSE65904, GSE35640 in Tumor Immune Single-Cell Hub (TISCH) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
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2026-11-01T18:14:53Z
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null
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paper
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PMID 36341357 full text
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data:geo:GSE120575
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dataset
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GEO GSE120575
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PMID 36341357 full text
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data:geo:GSE120575
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GEO GSE120575
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agent:corpus-assay-engine
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[0]
We detected cell proliferation of SKCM cells transfected with IRF2 siRNA. Then, we analyzed the immun
[1]
feration of SKCM cells transfected with IRF2 siRNA. Then, we analyzed the immunologic features
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paper_text_order:872
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36341357", "kind": "science-record", "revision": 4, "content_hash": "sha256:c4baf5dbf785135ec958fb3616ed1c113632764181785a70322b06241ebfc69f", "created_at": "2026-11-01T18:15:46Z", "updated_at": "2026-11-01T22:08:02Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A CD8+ T cell-associated immune gene panel for prediction of the prognosis and immunotherapeutic effect of melanoma.", "doi": "10.3389/fimmu.2022.1039565", "pmid": "36341357", "authors": ["Shanwen Sun", "Zhengke Zhi", "Yang Su", "Jingxian Sun", "Qianjun Li"], "journal": "Frontiers in immunology", "year": 2022, "abstract": "Background: Skin cutaneous melanoma (SKCM) is the most frequently encountered tumor of the skin. Immunotherapy has opened a new horizon in melanoma treatment. We aimed to construct a CD8+ T cell-associated immune gene prognostic model (CDIGPM) for SKCM and unravel the immunologic features and the benefits of immunotherapy in CDIGPM-defined SKCM groups.\nMethod: Single-cell SKCM transcriptomes were utilized in conjunction with immune genes for the screening of CD8+ T cell-associated immune genes (CDIGs) for succeeding assessment. Thereafter, through protein-protein interaction (PPI) networks analysis, univariate COX analysis, and multivariate Cox analysis, six genes (MX1, RSAD2, IRF2, GBP2, IFITM1, and OAS2) were identified to construct a CDIGPM. We detected cell proliferation of SKCM cells transfected with IRF2 siRNA. Then, we analyzed the immunologic features and the benefits of immunotherapy in CDIGPM-defined groups.\nResults: The overall survival (OS) was much better in low-CDIGPM group versus high CDIGPM group in TCGA dataset and GSE65904 dataset. On the whole, the results unfolded that a low CDIGPM showed relevance to immune response-correlated pathways, high expressions of CTLA4 and PD-L1, a high infiltration rate of CD8+ T cells, and more benefits from immunotherapy.\nConclusion: CDIGPM is an good model to predict the prognosis, the potential immune escape from immunotherapy for SKCM, and define immunologic and molecular features.", "claims": [{"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36341357", "locator": "sections[17] \"Data availability statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The low-CDIGPM group showed better overall survival, enrichment of immune-response-related pathways, higher CTLA4 and PD-L1 expression, greater CD8+ T-cell infiltration, and greater benefit from immunotherapy.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36341357", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The overall survival (OS) was much better in low-CDIGPM group versus high CDIGPM group in TCGA dataset and GSE65904 dataset."}, {"asset": "source:pmid:36341357", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "On the whole, the results unfolded that a low CDIGPM showed relevance to immune response-correlated pathways, high expressions of CTLA4 and PD-L1, a high infiltration rate of CD8+ T cells, and more benefits from immunotherapy."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The low-CDIGPM group showed better overall survival, enrichment of immune-response-related pathways, higher CTLA4 and PD-L1 expression, greater CD8+ T-cell infiltration, and greater benefit from immunotherapy.", "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:36341357"], "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:GSE120575"], "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:GSE120575"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36341357", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fimmu.2022.1039565", "sha256": "sha256:b741c39003110a6129a430a2508ff7cc487bc88eddcdcc5b7b4c63b4089d55ba", "bytes": 24506, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fimmu.2022.1039565", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9633226", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE120575", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE120575", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE120575", "version": null, "note": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/geo/, GSE120575.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM3403554", "GSM3403555", "GSM3403556", "GSM3403557", "GSM3403558", "GSM3403559", "GSM3403560", "GSM3403561", "GSM3403562", "GSM3403563", "GSM3403564", "GSM3403565", "GSM3403566", "GSM3403567", "GSM3403568", "GSM3403569", "GSM3403570", "GSM3403571", "GSM3403572", "GSM3403573", "GSM3403574", "GSM3403575", "GSM3403576", "GSM3403577", "GSM3403578", "GSM3403579", "GSM3403580", "GSM3403581", "GSM3403582", "GSM3403583", "GSM3403584", "GSM3403585", "GSM3403586", "GSM3403587", "GSM3403588", "GSM3403589", "GSM3403590", "GSM3403591", "GSM3403592", "GSM3403593", "GSM3403594", "GSM3403595", "GSM3403596", "GSM3403597", "GSM3403598", "GSM3403599", "GSM3403600", "GSM3403601"], "sample_count": 48, "group_sizes": null, "group_sizes_basis": null, "platform": "18573", "taxon": "Homo sapiens", "title": "Defining T cell states associated with response to checkpoint immunotherapy in melanoma", "resolution_checked_at": "2026-11-01T18:46:34Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE35640", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE35640", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE35640", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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