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pmid:36046784

Exploration of the immune microenvironment of breast cancer in large population cohorts.

Youyuan Deng · Jianguo Wang · Zhiya Hu · Yurong Cai · Yiping Xu · Ke Xu

Frontiers in endocrinology · 2022 doi:10.3389/fendo.2022.955630

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title
Exploration of the immune microenvironment of breast cancer in large population cohorts.
doi
10.3389/fendo.2022.955630
pmid
36046784
authors array · 6 items
[0]
Youyuan Deng
[1]
Jianguo Wang
[2]
Zhiya Hu
[3]
Yurong Cai
[4]
Yiping Xu
[5]
Ke Xu
journal
Frontiers in endocrinology
year
2022
abstract
Tumor immune microenvironment is associated with tumor progression. However, previous studies have not fully explored the breast cancer (BC) immune microenvironment. All the data analyzed in this study were obtained from the open-access database, including The Cancer Genome Atlas, Gene Expression Omnibus (TCGA), and cBioPortal databases. R software v4.0 and SPSS 13.0 were used to perform all the statistical analysis. Firstly, the clinical and expression profile information of TCGA, GSE20685, GSE20711, GSE48390, GSE58812, and METABRIC cohorts was collected. Then, 53 immune terms were quantified using the single-sample Gene Set Enrichment Analysis (ssGSEA) algorithm. A prognosis model based on HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score was established, which showed great prognosis prediction efficiency in both training group and validation group. A nomogram was then established for a better clinical application. Clinical correlation showed that elderly BC patients might have a higher riskscore. Pathway enrichment analysis showed that the pathway of oxidative phosphorylation, E2F targets, hedgehog signaling, adipogenesis, DNA repair, glycolysis, heme metabolism, and mTORC1 signaling was activated in the high-risk group. Moreover, Tumor Immune Dysfunction and Exclusion and Genomics of Drug Sensitivity in Cancer analysis showed that low-risk patients might be more sensitive to PD-1 therapy, cisplatin, gemcitabine, paclitaxel, and sunitinib. Finally, four genes, XCL1, XCL2, TNFRSF17, and IRF4, were identified for risk group classification. In summary, our signature is a useful tool for the prognosis and prediction of the drug sensitivity of BC.
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Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B ).
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sections[13] "Prognosis model construction" paragraph 2
quote
Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B ).
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.
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sections[20] "Data availability statement" paragraph 2
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.
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In summary, our signature is a useful tool for the prognosis and prediction of the drug sensitivity of BC.
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In summary, our signature is a useful tool for the prognosis and prediction of the drug sensitivity of BC.
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In summary, our signature is a useful tool for the prognosis and prediction of the drug sensitivity of BC.
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access_statement_kind
data_availability_statement
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sample_count
81
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null
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null
platform
570
taxon
Homo sapiens
title
Concurrent Gene Signatures for Han Chinese Breast Cancers [Affymetrix]
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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false
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data:geo:GSE58812
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null
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.
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GEO
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GEO accession URL
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.
access_statement_kind
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sample_count
107
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null
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null
platform
570
taxon
Homo sapiens
title
Gene-expression molecular subtyping of triple-negative breast cancer tumours: importance of immune response
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
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false
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asset:data:geo:GSE58812 licence not read
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complete
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Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B ).
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evidence object · 3 fields
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Automated Assays Laravel application and simulated adapters
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.
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The paper names GSE20685, GSE20711, GSE48390, GSE58812 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B ).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36046784", "kind": "science-record", "revision": 3, "content_hash": "sha256:5b446d8b26c6d586343103687f67ce77dde471f333d95dd4c45cda77f55ed1d9", "created_at": "2026-11-01T18:15:13Z", "updated_at": "2026-11-01T21:28:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Exploration of the immune microenvironment of breast cancer in large population cohorts.", "doi": "10.3389/fendo.2022.955630", "pmid": "36046784", "authors": ["Youyuan Deng", "Jianguo Wang", "Zhiya Hu", "Yurong Cai", "Yiping Xu", "Ke Xu"], "journal": "Frontiers in endocrinology", "year": 2022, "abstract": "Tumor immune microenvironment is associated with tumor progression. However, previous studies have not fully explored the breast cancer (BC) immune microenvironment. All the data analyzed in this study were obtained from the open-access database, including The Cancer Genome Atlas, Gene Expression Omnibus (TCGA), and cBioPortal databases. R software v4.0 and SPSS 13.0 were used to perform all the statistical analysis. Firstly, the clinical and expression profile information of TCGA, GSE20685, GSE20711, GSE48390, GSE58812, and METABRIC cohorts was collected. Then, 53 immune terms were quantified using the single-sample Gene Set Enrichment Analysis (ssGSEA) algorithm. A prognosis model based on HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score was established, which showed great prognosis prediction efficiency in both training group and validation group. A nomogram was then established for a better clinical application. Clinical correlation showed that elderly BC patients might have a higher riskscore. Pathway enrichment analysis showed that the pathway of oxidative phosphorylation, E2F targets, hedgehog signaling, adipogenesis, DNA repair, glycolysis, heme metabolism, and mTORC1 signaling was activated in the high-risk group. Moreover, Tumor Immune Dysfunction and Exclusion and Genomics of Drug Sensitivity in Cancer analysis showed that low-risk patients might be more sensitive to PD-1 therapy, cisplatin, gemcitabine, paclitaxel, and sunitinib. Finally, four genes, XCL1, XCL2, TNFRSF17, and IRF4, were identified for risk group classification. In summary, our signature is a useful tool for the prognosis and prediction of the drug sensitivity of BC.", "claims": [{"id": "claim-method", "statement": "Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . 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This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36046784", "locator": "sections[20] \"Data availability statement\" paragraph 2", "quote": "Publicly available datasets were analyzed in this study. 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Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B )."}}, {"id": "method-2", "family": "correlation_analysis", "specific": "spearman", "label": "Correlation analysis", "dsl_operations": ["spearman_rho"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["paired_numeric_columns"], "evidence": {"score": 0.8, "band": "high", "quote": "Spearman correlation"}}, {"id": "method-3", "family": "network_analysis", "specific": "pathway_enrichment", "label": "Network / pathway analysis", "dsl_operations": ["pathway_enrich"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["edge_list"], "evidence": {"score": 0.7, "band": "medium", "quote": "Pathway enrichment"}}], "targets": [], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"tier": "R1", "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": {"tier": "R1", "reachable": true, "accessions": ["GSE20685", "GSE20711", "GSE48390", "GSE58812"], "resolved_accessions": ["GSE20685", "GSE20711", "GSE48390", "GSE58812"], "statements": ["Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov/; https://www.ncbi.nlm.nih.gov/gds/."], "basis": "The paper names GSE20685, GSE20711, GSE48390, GSE58812 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["cox_ph"], "assets": ["source:pmid:36046784", "data:geo:GSE20685"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE20685"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T18:02:43Z", "independence": "single_reader"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 11453, "completion_tokens": 2196, "cached_tokens": 264}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:36046784", "type": "paper", "label": "pmid:36046784"}, {"id": "source:pmid:36046784", "type": "manuscript", "label": "PMID 36046784 full text"}, {"id": "data:geo:GSE20685", "type": "dataset", "label": "GEO GSE20685"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:36046784", "type": "paper", "label": "pmid:36046784"}, {"id": "source:pmid:36046784", "type": "manuscript", "label": "PMID 36046784 full text"}, {"id": "data:geo:GSE20685", "type": "dataset", "label": "GEO GSE20685"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-36046784", "type": "extraction", "used": ["source:pmid:36046784"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE20685", "type": "accession_resolution", "used": ["data:geo:GSE20685"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:36046784", "parent_hash": "sha256:df166297c5a35909e0d647e279c1d9cd7482ef7a5fc6abf039bee97b3c21118c", "fork_of": null, "generation": 2}, "gaps": ["asset:data:geo:GSE20685 licence not read", "asset:data:geo:GSE20685 not downloaded", "asset:data:geo:GSE20711 licence not read", "asset:data:geo:GSE20711 not downloaded", "asset:data:geo:GSE48390 licence not read", "asset:data:geo:GSE48390 not downloaded", "asset:data:geo:GSE58812 licence not read", "asset:data:geo:GSE58812 not downloaded", "execution.not_run", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Firstly, univariate Cox regression and LASSO analysis were performed to screen the prognosis-related immune terms based on the TCGA database ( Figure 2A ). The terms meeting the criteria of univariate Cox regression are shown in Table S7 . Then, multivariate Cox regression analysis identified five immune terms used for model construction, namely, HER2_Immune_PCA, IL12_score, IL13_score, IL4_score, and IR7_score ( Figure 2B )."], "order_basis": "analysis_only", "id": "assay:1"}]}