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pmid:34382341

Identification of a novel 10 immune-related genes signature as a prognostic biomarker panel for gastric cancer.

Tingna Chen · Chaogang Yang · Rongzhang Dou · Bin Xiong

Cancer medicine · 2021 doi:10.1002/cam4.4180

Paper

complete

Experiment

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Data

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Analysis

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Execution

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title
Identification of a novel 10 immune-related genes signature as a prognostic biomarker panel for gastric cancer.
doi
10.1002/cam4.4180
pmid
34382341
authors array · 4 items
[0]
Tingna Chen
[1]
Chaogang Yang
[2]
Rongzhang Dou
[3]
Bin Xiong
journal
Cancer medicine
year
2021
abstract
BACKGROUND: Emerging evidence indicates that immune infiltrating cells in tumor microenvironment (TME) correlates with the development and progression of gastric cancer (GC). This study aimed to systematically investigate the immune-related genes (IRGs) to develop a prognostic signature to predict the overall survival (OS) in GC. METHOD: The gene expression profiles of training dataset (GSE62254), validation dataset I (GSE15459), and validation dataset II (GSE84437) were retrieved from GEO and TCGA databases. In the present study, we developed a 10 IRGs prognostic signature with the combination of weighted gene co-expression network analysis (WGCNA) and least absolute shrinkage and selection operator method (LASSO) COX model. RESULTS: In the training dataset, the accuracy of the signature was 0.681, 0.741, and 0.72 in predicting 1, 3, and 5-year OS separately. The signature also had good performance in validation dataset Ⅰ with the accuracy of 0.57, 0.619, and 0.694, and in validation dataset Ⅱ with the accuracy of 0.559, 0.624, and 0.585. Then, we constructed a nomogram using the signature and clinical information which had strong discrimination ability with the c-index of 0.756. In the immune infiltration analysis, the signature was correlated with multiple immune infiltrating cells such as CD8 T cells, CD4 memory T cells, NK cells, and macrophages. Furthermore, several significant pathways were enriched in gene set enrichment analysis (GSEA) analysis, including TGF-beta signaling pathway and Wnt signaling pathway. CONCLUSION: The signature of 10 IRGs we identified can effectively predict the prognosis of GC and provides new insight into discovering candidate prognostic biomarkers of GC.
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The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/).
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sample_count
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group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Molecular analysis of gastric cancer identifies discrete subtypes associated with distinct clinical characteristics and survival outcomes: the ACRG (Asian Cancer Research Group) study [gastric tumors]
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[3] object · 15 fields
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data:geo:GSE84437
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note
The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/).
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/).
access_statement_kind
data_availability_statement
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[482]
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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
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[4] object · 16 fields
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asset:table:pmid:34382341:1
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jats-table
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null
note
Information for 10 IRGs signature screened by LASSO Cox regression
structure object · 5 fields
pmcid
PMC8446556
section_index
12
section_title
Construction of the prognostic classifier
row_count
11
column_count
6
table object · 8 fields
label
TABLE 1
caption
Information for 10 IRGs signature screened by LASSO Cox regression
rows array · 11 items
[0] array · 6 items
[0]
Symbol
[1]
Coefficient
[2]
p value
[3]
HR
[4]
Low 95% CI
[5]
High 95% CI
[1] array · 6 items
[0]
BMPR1B
[1]
0.12784
[2]
0.3497
[3]
1.1364
[4]
0.8693
[5]
1.486
[2] array · 6 items
[0]
GHR
[1]
0.02741
[2]
0.8168
[3]
1.0278
[4]
0.8151
[5]
1.296
[3] array · 6 items
[0]
IL11RA
[1]
0.3035
[2]
0.382
[3]
1.3546
[4]
0.6859
[5]
2.675
[4] array · 6 items
[0]
INHBB
[1]
0.34105
[2]
9.75E−05
[3]
1.4064
[4]
1.1847
[5]
1.67
[5] array · 6 items
[0]
NPR3
[1]
0.15621
[2]
0.5495
[3]
1.1691
[4]
0.701
[5]
1.95
[6] array · 6 items
[0]
OBP2A
[1]
−0.84737
[2]
0.1554
[3]
0.4285
[4]
0.1331
[5]
1.38
[7] array · 6 items
[0]
PTN
[1]
0.0486
[2]
0.7633
[3]
1.0498
[4]
0.7651
[5]
1.44
[8] array · 6 items
[0]
R3HDML
[1]
−0.78119
[2]
0.0834
[3]
0.4579
[4]
0.1891
[5]
1.109
[9] array · 6 items
[0]
TAC1
[1]
0.03729
[2]
0.5914
[3]
1.038
[4]
0.9058
[5]
1.189
[10] array · 6 items
[0]
TPM2
[1]
0.17652
[2]
0.5758
[3]
1.1931
[4]
0.6428
[5]
2.214
locator
section[12]/table-wrap[1]#cam44180-tbl-0001
[5] object · 16 fields
id
asset:table:pmid:34382341:2
role
table
format
jats-table
media_type
application/vnd.jats.table+json
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null
sha256
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Univariate and multivariate Cox regression analysis of clinical information and RS
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PMC8446556
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13
section_title
Verification in two external datasets
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18
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TABLE 2
caption
Univariate and multivariate Cox regression analysis of clinical information and RS
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Univariate Cox regression analysis
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Multivariate Cox regression analysis
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HR (95%CI)
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p value
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Risk factors
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HR (95%CI)
[5]
p value
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[0]
Gender (male vs. female)
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0.90(0.65–1.27)
[2]
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Gender (male vs. female)
[4]
1.07(0.75–1.52)
[5]
0.716
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0.217
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Age (≥60 vs. <60)
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2.10(1.46–3.00)
[5]
<0.001
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Stage
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3.41(2.34–4.96)
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<0.001
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Stage
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1.32(0.89–1.96)
[5]
0.175
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RS
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2.72(2.15–3.44)
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RS
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2.76(2.13–3.58)
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<0.001
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Risk factors
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HR (95%CI)
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p value
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Risk factors
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HR (95%CI)
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p value
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Gender (male vs. female)
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0.127
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Gender (male vs. female)
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Age (≥60 vs. <60)
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1.02(1.00–1.03)
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RS
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RS
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<0.001
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Validation dataset II
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Risk factors
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HR (95%CI)
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p value
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Risk factors
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HR (95%CI)
[5]
p value
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[0]
Gender (male vs. female)
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1.26(0.93–1.70)
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0.141
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Gender (male vs. female)
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1.24(0.91–1.67)
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Age (≥60 vs. <60)
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1.94(1.45–2.61)
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<0.001
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RS
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1.54(1.14–2.07)
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0.005
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RS
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1.72 (1.27–2.33)
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section[13]/table-wrap[1]#cam44180-tbl-0002
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The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/).
basis
The paper names GSE62254, GSE15459, 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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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34382341", "kind": "science-record", "revision": 4, "content_hash": "sha256:577355727bf230c66a6396e4594ee3c724cfa2bb116d16fe1f5d12371c136c90", "created_at": "2026-11-01T15:41:47Z", "updated_at": "2026-11-01T21:26:00Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of a novel 10 immune-related genes signature as a prognostic biomarker panel for gastric cancer.", "doi": "10.1002/cam4.4180", "pmid": "34382341", "authors": ["Tingna Chen", "Chaogang Yang", "Rongzhang Dou", "Bin Xiong"], "journal": "Cancer medicine", "year": 2021, "abstract": "BACKGROUND: Emerging evidence indicates that immune infiltrating cells in tumor microenvironment (TME) correlates with the development and progression of gastric cancer (GC). This study aimed to systematically investigate the immune-related genes (IRGs) to develop a prognostic signature to predict the overall survival (OS) in GC.\nMETHOD: The gene expression profiles of training dataset (GSE62254), validation dataset I (GSE15459), and validation dataset II (GSE84437) were retrieved from GEO and TCGA databases. In the present study, we developed a 10 IRGs prognostic signature with the combination of weighted gene co-expression network analysis (WGCNA) and least absolute shrinkage and selection operator method (LASSO) COX model.\nRESULTS: In the training dataset, the accuracy of the signature was 0.681, 0.741, and 0.72 in predicting 1, 3, and 5-year OS separately. The signature also had good performance in validation dataset Ⅰ with the accuracy of 0.57, 0.619, and 0.694, and in validation dataset Ⅱ with the accuracy of 0.559, 0.624, and 0.585. Then, we constructed a nomogram using the signature and clinical information which had strong discrimination ability with the c-index of 0.756. In the immune infiltration analysis, the signature was correlated with multiple immune infiltrating cells such as CD8 T cells, CD4 memory T cells, NK cells, and macrophages. Furthermore, several significant pathways were enriched in gene set enrichment analysis (GSEA) analysis, including TGF-beta signaling pathway and Wnt signaling pathway.\nCONCLUSION: The signature of 10 IRGs we identified can effectively predict the prognosis of GC and provides new insight into discovering candidate prognostic biomarkers of GC.", "claims": [{"id": "claim-data-access", "statement": "The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34382341", "locator": "sections[22] \"DATA AVAILABILITY STATEMENT\" paragraph 2", "quote": "The data that support the findings of this study are openly available in ImmPort database (https://immport.niaid.nih.gov/ ), Gene Expression Omnibus (GEO) database (GSE62254, GSE15459, GSE84437), and The Cancer Genome Atlas (TCGA) database (https://genomecancer.ucsc.edu/)."}], "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:34382341"], "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:GSE15459"], "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:GSE15459"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34382341", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1002/cam4.4180", "sha256": 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