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pmid:35621244

Construction of ovarian metastasis-related immune signature predicting prognosis of gastric cancer patients.

Jianpeng Gao · Shiying Huo · Yu Zhang · Zhenxiong Zhao · Hongda Pan · Xiaowen Liu

Cancer medicine · 2023 doi:10.1002/cam4.4857

Paper

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Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35621244
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science-record
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2026-11-01T18:14:32Z
updated_at
2026-11-01T22:06:37Z
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paper object · 10 fields
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title
Construction of ovarian metastasis-related immune signature predicting prognosis of gastric cancer patients.
doi
10.1002/cam4.4857
pmid
35621244
authors array · 6 items
[0]
Jianpeng Gao
[1]
Shiying Huo
[2]
Yu Zhang
[3]
Zhenxiong Zhao
[4]
Hongda Pan
[5]
Xiaowen Liu
journal
Cancer medicine
year
2023
abstract
BACKGROUND: Ovarian metastasis (OM) results in poor survival of gastric cancer (GC) patients. While immunotherapy has emerged as a promising approach for late-stage GC, validated immune-related prognostic signatures still remain in need. In this study, we constructed an ovarian metastasis- and immune-related prognostic signature (OMIRPS), characterized the molecular and immune features of OMIRPS-categorized subgroups and predicted their potential response to immunotherapy. METHODS: Three individual cohorts were used to construct and evaluate OMIRPS: RNA-seq of matched primary GC and OM from Fudan University Shanghai Cancer Center (FUSCC) (discovery cohort, n = 4), The Cancer Genome Atlas (TCGA) (training cohort, n = 544) and GSE84437 (validation cohort, n = 433). Differentially expressed genes (DEGs) identified between primary GC and OM and immune-related genes (IRGs) from the ImmPort and InnateDB databases were used to identify immune-related prognostic hub genes, which were further used to construct OMIRPS by using LASSO regression analysis. Prognosis, molecular characteristics, immune features, and differential immunotherapy efficacy between different OMIRPS subgroups were analyzed. RESULTS: Functional analyses of DEGs revealed the significance of immune-related signatures and pathways in the OM. Immune-related prognostic hub genes including TNFRSF18, CARD11, BCL11B, NRP1, BNIP3L, and ATF3 were utilized to construct OMIRPS, which was identified as an independent prognostic factor. Comprehensive analyses unveiled the distinctive molecular and immune characteristics of OMIRPS-high and -low subgroup in regard to enriched pathways, mutation rate, tumor mutation burden, microsatellite instability status, infiltrated immune cell, immune exclusion score, and the prediction of immunotherapy efficacy. Additionally, OMIRPS was associated with Immune Subtypes with borderline significance. CONCLUSIONS: RNA-seq of paired primary and ovarian metastatic tumors unveiled the significance of immune-related pathways and tumor immune microenvironment in OM. OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.
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A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages.
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sections[8] "Construction and validation of ovarian metastasis‐ and immune‐related and prognostic signature (OMIRPS)" paragraph 2
quote
A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages.
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The datasets used for the current study are available from the corresponding authors upon reasonable request.
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sections[30] "DATA AVAILABILITY STATEMENT" paragraph 2
quote
The datasets used for the current study are available from the corresponding authors upon reasonable request.
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[2] object · 6 fields
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OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.
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qualitative
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null
evidence array · 1 item
[0] object · 3 fields
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sections[0] "Abstract" paragraph 4
quote
OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.
state
complete
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OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.
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Apply the paper's statistical method to the resolved series and compare the result with the published target.
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[478]
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[479]
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[481]
GSM4419532
[482]
GSM4419533
sample_count
483
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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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gaps array · 2 items
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method-1
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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cox_ph
missing_operations array · 0 items
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data_shapes array · 1 item
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time_to_event_with_censoring
evidence object · 3 fields
score
1
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verbatim
quote
A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages.
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group_comparison
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wilcoxon
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Group comparison
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missing_operations array · 1 item
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false
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evidence object · 3 fields
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Wilcoxon
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differential_expression
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eshold was set as |log2[fold change (FC)]| > 1, and False D
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False Discovery Rates (FDR) <0
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[0]
count_matrix_with_condition
evidence object · 3 fields
score
0.8
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quote
limma
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correlation_analysis
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Correlation analysis
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[0]
pearson_r
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evidence object · 3 fields
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0.8
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Pearson correlation
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method-5
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sequence_alignment
specific
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label
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[0]
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[1]
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capability object · 3 fields
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complete
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capability:computational_analysis
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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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nothing:replicable_now
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method object · 5 fields
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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.
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tier
R1
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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
R1
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true
accessions array · 1 item
[0]
GSE84437
resolved_accessions array · 1 item
[0]
GSE84437
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[0]
The datasets used for the current study are available from the corresponding authors upon reasonable request.
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.
can_run object · 3 fields
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[0]
cox_ph
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source:pmid:35621244
[1]
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data:geo:GSE84437
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T17:47:40Z
independence
single_reader
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verbatim
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verbatim
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5
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extraction
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complete
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review.human_critique
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pmid:35621244
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paper
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pmid:35621244
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source:pmid:35621244
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manuscript
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PMID 35621244 full text
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data:geo:GSE84437
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dataset
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GEO GSE84437
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paper
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pmid:35621244
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source:pmid:35621244
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PMID 35621244 full text
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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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extraction
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agent:minimax-reader
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accession_resolution
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agent:corpus-assay-engine
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[0]
were used to construct and evaluate OMIRPS: RNA-seq of matched primary GC and OM from Fudan Univ
[1]
s with borderline significance. CONCLUSIONS: RNA-seq of paired primary and ovarian metastatic tum
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paper_text_order:621
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assay:1
[1] object · 11 fields
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f2132e96ae6c7a4e
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A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35621244", "kind": "science-record", "revision": 4, "content_hash": "sha256:4a50e20b7d7b09b107ad4ea4a97c89288777403ec2b3fbca01ee1cd98fb91942", "created_at": "2026-11-01T18:14:32Z", "updated_at": "2026-11-01T22:06:37Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction of ovarian metastasis-related immune signature predicting prognosis of gastric cancer patients.", "doi": "10.1002/cam4.4857", "pmid": "35621244", "authors": ["Jianpeng Gao", "Shiying Huo", "Yu Zhang", "Zhenxiong Zhao", "Hongda Pan", "Xiaowen Liu"], "journal": "Cancer medicine", "year": 2023, "abstract": "BACKGROUND: Ovarian metastasis (OM) results in poor survival of gastric cancer (GC) patients. While immunotherapy has emerged as a promising approach for late-stage GC, validated immune-related prognostic signatures still remain in need. In this study, we constructed an ovarian metastasis- and immune-related prognostic signature (OMIRPS), characterized the molecular and immune features of OMIRPS-categorized subgroups and predicted their potential response to immunotherapy.\nMETHODS: Three individual cohorts were used to construct and evaluate OMIRPS: RNA-seq of matched primary GC and OM from Fudan University Shanghai Cancer Center (FUSCC) (discovery cohort, n = 4), The Cancer Genome Atlas (TCGA) (training cohort, n = 544) and GSE84437 (validation cohort, n = 433). Differentially expressed genes (DEGs) identified between primary GC and OM and immune-related genes (IRGs) from the ImmPort and InnateDB databases were used to identify immune-related prognostic hub genes, which were further used to construct OMIRPS by using LASSO regression analysis. Prognosis, molecular characteristics, immune features, and differential immunotherapy efficacy between different OMIRPS subgroups were analyzed.\nRESULTS: Functional analyses of DEGs revealed the significance of immune-related signatures and pathways in the OM. Immune-related prognostic hub genes including TNFRSF18, CARD11, BCL11B, NRP1, BNIP3L, and ATF3 were utilized to construct OMIRPS, which was identified as an independent prognostic factor. Comprehensive analyses unveiled the distinctive molecular and immune characteristics of OMIRPS-high and -low subgroup in regard to enriched pathways, mutation rate, tumor mutation burden, microsatellite instability status, infiltrated immune cell, immune exclusion score, and the prediction of immunotherapy efficacy. Additionally, OMIRPS was associated with Immune Subtypes with borderline significance.\nCONCLUSIONS: RNA-seq of paired primary and ovarian metastatic tumors unveiled the significance of immune-related pathways and tumor immune microenvironment in OM. OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.", "claims": [{"id": "claim-method", "statement": "A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35621244", "locator": "sections[8] \"Construction and validation of ovarian metastasis‐ and immune‐related and prognostic signature (OMIRPS)\" paragraph 2", "quote": "A least absolute shrinkage and selection operator (LASSO) Cox regression model were performed on prognostic hub genes with “glmnet” and “survival” packages."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used for the current study are available from the corresponding authors upon reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35621244", "locator": "sections[30] \"DATA AVAILABILITY STATEMENT\" paragraph 2", "quote": "The datasets used for the current study are available from the corresponding authors upon reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35621244", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "OMIRPS served as a promising biomarker to predict the prognosis of GC patients and distinguish the molecular features, immune characteristics, and efficacy of immunotherapy between different subgroups.", "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:35621244"], "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:35621244", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1002/cam4.4857", "sha256": "sha256:6ff1ffe7054e0f477991677908cc56802d8e507fad06d39fa04f8121406a5445", "bytes": 60393, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1002/cam4.4857", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9844635", "source": "europe_pmc_fulltext", "coverage": "whole_body", "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 datasets used for the current study are available from the corresponding authors upon reasonable request.", "structure": {"repository": 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