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pmid:35692814

Development of a Novel Immune-Related Gene Signature to Predict Prognosis and Immunotherapeutic Efficiency in Gastric Cancer.

Dongliang Liu · Yuanmin Xu · Yu Fang · Kongwang Hu

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.885553

Paper

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Experiment

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Data

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pmid:35692814
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title
Development of a Novel Immune-Related Gene Signature to Predict Prognosis and Immunotherapeutic Efficiency in Gastric Cancer.
doi
10.3389/fgene.2022.885553
pmid
35692814
authors array · 4 items
[0]
Dongliang Liu
[1]
Yuanmin Xu
[2]
Yu Fang
[3]
Kongwang Hu
journal
Frontiers in genetics
year
2022
abstract
Background: Gastric cancer (GC) is the fifth most common malignancy and the third leading cause of tumor-related deaths globally. Herein, we attempted to build a novel immune-related gene (IRG) signature that could predict the prognosis and immunotherapeutic efficiency for GC patients. Methods: The mRNA transcription data and corresponding clinical data of GC were downloaded from The Cancer Genome Atlas (TCGA) database as the training group and the GSE84437 data set as the testing cohort, followed by acquisition of IRGs from the InnateDB resource and ImmPort database. Using the univariate Cox regression analysis, an IRG signature was developed. Several immunogenomic analyses were performed to illustrate the associations between the immune risk score and tumor mutational burden, immune cell infiltrations, function of immune infiltration, clinical characteristics, immune subtype, and immunotherapeutic response. Results: The analysis of 343 GC samples and 30 normal samples from the TCGA database gave rise to 8,713 differentially expressed genes (DEGs) and 513 differentially expressed immune-related genes (DEIRGs) were extracted. The novel IRG signature contained eight DEIRGs (FABP4, PI15, RNASE2, CGB5, INHBE, RLN2, DUSP1, and CD36) and was found to serve as an independent predictive and prognostic factor for GC. Then, the GC patients were separated into the high- and low-risk groups based on the median risk score, wherein the low-risk group presented a better prognosis and was more sensitive to immunotherapy than did the high-risk group. According to the time-dependent ROC curves and AUCs, the immunotherapeutic value of the signature was better than the Tumor Immune Dysfunction and Exclusion (TIDE) and T-cell inflammatory signature (TIS) scores. In addition, the AUCs of the risk score for predicting 1-, 2-, and 3-year OS were 0.675, 0.682, and 0.710, respectively, which indicated that the signature had great predictive power. Conclusion: This study presents a novel IRG signature based on the tumor immune microenvironment, which could improve the prediction of the prognosis and immunotherapeutic efficiency for GC patients. The powerful signature may serve as novel biomarkers and provide therapeutic targets for precision oncology in clinical practice.
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The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot.
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sections[6] "Establishment and Validation of the Immune-Related Risk Signature" paragraph 2
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The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot.
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The data sets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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sections[24] "Data Availability Statement" paragraph 2
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The data sets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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Using the univariate Cox regression analysis, an IRG signature was developed.
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Using the univariate Cox regression analysis, an IRG signature was developed.
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Using the univariate Cox regression analysis, an IRG signature was developed.
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GSM4419531
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[482]
GSM4419533
sample_count
483
group_sizes
null
group_sizes_basis
null
platform
6947
taxon
Homo sapiens
title
Molecular subtypes in gastric cancer.
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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state
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method-1
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survival_analysis
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cox_proportional_hazards
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cox_ph
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evidence object · 3 fields
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quote
The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot.
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gaps array · 0 items
capability object · 3 fields
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complete
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capability:computational_analysis
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statistical_regression
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differential_expression
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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complete
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cox_ph
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
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capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
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[0]
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[0]
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[0]
The data sets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
basis
The paper names GSE84437 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
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independence
single_reader
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id
pmid:35692814
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paper
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pmid:35692814
[1] object · 3 fields
id
source:pmid:35692814
type
manuscript
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PMID 35692814 full text
[2] object · 3 fields
id
data:geo:GSE84437
type
dataset
label
GEO GSE84437
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
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pmid:35692814
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paper
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pmid:35692814
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id
source:pmid:35692814
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PMID 35692814 full text
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id
data:geo:GSE84437
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dataset
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GEO GSE84437
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agent:corpus-assay-engine
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id
activity-read-35692814
type
extraction
used array · 1 item
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agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE84437
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accession_resolution
used array · 1 item
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agent:corpus-assay-engine
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agent:minimax-reader
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gaps array · 6 items
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The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot.
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analysis_only
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35692814", "kind": "science-record", "revision": 3, "content_hash": "sha256:287ea005c53302d11ec851ac2ad5f8e5d933a7daabe0fb678d6a6c3f5eb4fd1c", "created_at": "2026-11-01T18:14:39Z", "updated_at": "2026-11-01T21:28:05Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development of a Novel Immune-Related Gene Signature to Predict Prognosis and Immunotherapeutic Efficiency in Gastric Cancer.", "doi": "10.3389/fgene.2022.885553", "pmid": "35692814", "authors": ["Dongliang Liu", "Yuanmin Xu", "Yu Fang", "Kongwang Hu"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "Background: Gastric cancer (GC) is the fifth most common malignancy and the third leading cause of tumor-related deaths globally. Herein, we attempted to build a novel immune-related gene (IRG) signature that could predict the prognosis and immunotherapeutic efficiency for GC patients. Methods: The mRNA transcription data and corresponding clinical data of GC were downloaded from The Cancer Genome Atlas (TCGA) database as the training group and the GSE84437 data set as the testing cohort, followed by acquisition of IRGs from the InnateDB resource and ImmPort database. Using the univariate Cox regression analysis, an IRG signature was developed. Several immunogenomic analyses were performed to illustrate the associations between the immune risk score and tumor mutational burden, immune cell infiltrations, function of immune infiltration, clinical characteristics, immune subtype, and immunotherapeutic response. Results: The analysis of 343 GC samples and 30 normal samples from the TCGA database gave rise to 8,713 differentially expressed genes (DEGs) and 513 differentially expressed immune-related genes (DEIRGs) were extracted. The novel IRG signature contained eight DEIRGs (FABP4, PI15, RNASE2, CGB5, INHBE, RLN2, DUSP1, and CD36) and was found to serve as an independent predictive and prognostic factor for GC. Then, the GC patients were separated into the high- and low-risk groups based on the median risk score, wherein the low-risk group presented a better prognosis and was more sensitive to immunotherapy than did the high-risk group. According to the time-dependent ROC curves and AUCs, the immunotherapeutic value of the signature was better than the Tumor Immune Dysfunction and Exclusion (TIDE) and T-cell inflammatory signature (TIS) scores. In addition, the AUCs of the risk score for predicting 1-, 2-, and 3-year OS were 0.675, 0.682, and 0.710, respectively, which indicated that the signature had great predictive power. Conclusion: This study presents a novel IRG signature based on the tumor immune microenvironment, which could improve the prediction of the prognosis and immunotherapeutic efficiency for GC patients. The powerful signature may serve as novel biomarkers and provide therapeutic targets for precision oncology in clinical practice.", "claims": [{"id": "claim-method", "statement": "The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35692814", "locator": "sections[6] \"Establishment and Validation of the Immune-Related Risk Signature\" paragraph 2", "quote": "The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data sets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35692814", "locator": "sections[24] \"Data Availability Statement\" paragraph 2", "quote": "The data sets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Using the univariate Cox regression analysis, an IRG signature was developed.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35692814", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Using the univariate Cox regression analysis, an IRG signature was developed."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Using the univariate Cox regression analysis, an IRG signature was developed.", "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:35692814"], "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:GSE84437"], "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:GSE84437"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35692814", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2022.885553", "sha256": "sha256:1c52c70d9e5ec7bc621c9d175aefd926cef19a27e0bcf9e2fdc53388313ef868", "bytes": 40751, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fgene.2022.885553", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9186121", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE84437", "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=GSE84437", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE84437", "version": null, "note": "The data sets presented in this study can be found in online repositories. 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"sample_count": 483, "group_sizes": null, "group_sizes_basis": null, "platform": "6947", "taxon": "Homo sapiens", "title": "Molecular subtypes in gastric cancer.", "resolution_checked_at": "2026-11-01T15:39:55Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}], "gaps": ["asset:data:geo:GSE84437 not downloaded", "asset:data:geo:GSE84437 licence not read"]}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "The univariate Cox regression analysis was carried out to identify the survival-related DEIRGs (p < 0.05), and the result was visualized as a forest plot."}}], "targets": [], "gaps": []}, 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