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pmid:37509156

Molecular Evolutionary Landscape of the Immune Microenvironment of Head and Neck Cancer.

Baoyi Shao · Zheng Ye · Bo Sun · Zhongdang Xiao

Biomolecules · 2023 doi:10.3390/biom13071120

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

absent

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title
Molecular Evolutionary Landscape of the Immune Microenvironment of Head and Neck Cancer.
doi
10.3390/biom13071120
pmid
37509156
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[0]
Baoyi Shao
[1]
Zheng Ye
[2]
Bo Sun
[3]
Zhongdang Xiao
journal
Biomolecules
year
2023
abstract
Head and neck cancer is a highly heterogeneous malignant tumor. Numerous studies have shown that the immune microenvironment of head and neck cancer has a significant impact on its occurrence and development, as well as its prognosis. However, there have been fewer studies related to the accurate immunophenotyping of head and neck cancer. In this study, we used gene expression profile information and clinical information from the TCGA-HNSC cohort (502 samples) and the GSE655858 cohort (270 samples) to identify and independently validate three immune subtypes (Cluster1-Cluster3) with different immune-related molecular profiles and clinical outcomes. Cluster2, which is mainly dominated by B-lymphocyte infiltration, was found to have the best prognosis. In addition, a support vector machine (SVM)-based classifier was constructed, which could accurately classify HNSC based on 19 genes. Furthermore, the results of the prognostic analysis showed activation of antibody-secreting B-lymphocyte function, which showed a good prognostic effect in all three immune subtypes of HNSC. Finally, the immune evolutionary landscape of HNSC was constructed in an attempt to explain the evolutionary pattern of the immune subtypes of HNSC. In summary, we provide a conceptual framework for understanding the tumor immune microenvironment in HNSC and demonstrate the importance of immune infiltration of B lymphocytes in HNSC. Further research is needed to assess the importance of these immunophenotypes in combination drug therapy and to provide a basis for screening appropriate patients for immunotherapy.
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The prognosis of immune subtypes was evaluated using the log-rank test and univariate cox regression model, with age as a covariate, and OS and DFS as the focus.
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sections[10] "2.8. Prognostic Evaluation of Immune Subtypes" paragraph 2
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The prognosis of immune subtypes was evaluated using the log-rank test and univariate cox regression model, with age as a covariate, and OS and DFS as the focus.
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Proteome profiling and clinical and transcriptome data about Head and neck cancer were downloaded from TCGA Database (https://portal.gdc.cancer.gov/) and GEO Database (https://www.ncbi.nlm.nih.gov/geo/). Please contact the author if you want to access the codes.
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sections[29] "notes" paragraph 1
quote
Proteome profiling and clinical and transcriptome data about Head and neck cancer were downloaded from TCGA Database (https://portal.gdc.cancer.gov/) and GEO Database (https://www.ncbi.nlm.nih.gov/geo/). Please contact the author if you want to access the codes.
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The Kaplan–Meier survival analysis showed that Cluster2 had the best prognosis, Cluster1 the worst, and Cluster3 was in between (hazard ratio: Cluster 2 > Cluster 3 > Cluster 1).
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sections[13] "3.1. Identification of Potential HNSC Immune Subtypes" paragraph 2
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The Kaplan–Meier survival analysis showed that Cluster2 had the best prognosis, Cluster1 the worst, and Cluster3 was in between (hazard ratio: Cluster 2 > Cluster 3 > Cluster 1).
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sections[13] "3.1. Identification of Potential HNSC Immune Subtypes" paragraph 2
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There is a significant difference in survival between the three immune subtypes (p = 0.01)
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The Kaplan–Meier survival analysis showed that Cluster2 had the best prognosis, Cluster1 the worst, and Cluster3 was in between (hazard ratio: Cluster 2 > Cluster 3 > Cluster 1).
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Proteome profiling and clinical and transcriptome data about Head and neck cancer were downloaded from TCGA Database (https://portal.gdc.cancer.gov/) and GEO Database (https://www.ncbi.nlm.nih.gov/geo/). Please contact the author if you want to access the codes.
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Gene expression patterns and TP53 mutations are associated with HPV RNA status, lymph node metastasis, and survival in head and neck cancer
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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 object · 4 fields
parent_id
pmid:37509156
parent_hash
sha256:2da09e5f61dce7a892e2d0ccd6a6d7b1584e17d20c29fafa190bcd319fc8e912
fork_of
null
gaps array · 6 items
[0]
asset:data:geo:GSE65858 licence not read
[1]
asset:data:geo:GSE65858 not downloaded
[2]
execution.not_run
[3]
review.human_critique
[4]
review.independent_reader
[5]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
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cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
The prognosis of immune subtypes was evaluated using the log-rank test and univariate cox regression model, with age as a covariate, and OS and DFS as the focus.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37509156", "kind": "science-record", "revision": 4, "content_hash": "sha256:300725e56ca1c5c3d2dd4f2ba0ce79e84306ffa1702bf09005b91296b0260608", "created_at": "2026-11-01T19:02:16Z", "updated_at": "2026-11-01T22:52:24Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Molecular Evolutionary Landscape of the Immune Microenvironment of Head and Neck Cancer.", "doi": "10.3390/biom13071120", "pmid": "37509156", "authors": ["Baoyi Shao", "Zheng Ye", "Bo Sun", "Zhongdang Xiao"], "journal": "Biomolecules", "year": 2023, "abstract": "Head and neck cancer is a highly heterogeneous malignant tumor. Numerous studies have shown that the immune microenvironment of head and neck cancer has a significant impact on its occurrence and development, as well as its prognosis. However, there have been fewer studies related to the accurate immunophenotyping of head and neck cancer. In this study, we used gene expression profile information and clinical information from the TCGA-HNSC cohort (502 samples) and the GSE655858 cohort (270 samples) to identify and independently validate three immune subtypes (Cluster1-Cluster3) with different immune-related molecular profiles and clinical outcomes. Cluster2, which is mainly dominated by B-lymphocyte infiltration, was found to have the best prognosis. In addition, a support vector machine (SVM)-based classifier was constructed, which could accurately classify HNSC based on 19 genes. Furthermore, the results of the prognostic analysis showed activation of antibody-secreting B-lymphocyte function, which showed a good prognostic effect in all three immune subtypes of HNSC. Finally, the immune evolutionary landscape of HNSC was constructed in an attempt to explain the evolutionary pattern of the immune subtypes of HNSC. In summary, we provide a conceptual framework for understanding the tumor immune microenvironment in HNSC and demonstrate the importance of immune infiltration of B lymphocytes in HNSC. Further research is needed to assess the importance of these immunophenotypes in combination drug therapy and to provide a basis for screening appropriate patients for immunotherapy.", "claims": [{"id": "claim-method", "statement": "The prognosis of immune subtypes was evaluated using the log-rank test and univariate cox regression model, with age as a covariate, and OS and DFS as the focus.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37509156", "locator": "sections[10] \"2.8. 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Please contact the author if you want to access the codes."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The Kaplan–Meier survival analysis showed that Cluster2 had the best prognosis, Cluster1 the worst, and Cluster3 was in between (hazard ratio: Cluster 2 > Cluster 3 > Cluster 1).", "kind": "quantitative", "target": {"value": 0.01, "unit": "p-value", "tolerance": null, "source": "There is a significant difference in survival between the three immune subtypes (p = 0.01)"}, "evidence": [{"asset": "source:pmid:37509156", "locator": "sections[13] \"3.1. Identification of Potential HNSC Immune Subtypes\" paragraph 2", "quote": "The Kaplan–Meier survival analysis showed that Cluster2 had the best prognosis, Cluster1 the worst, and Cluster3 was in between (hazard ratio: Cluster 2 > Cluster 3 > Cluster 1)."}, {"asset": "source:pmid:37509156", "locator": "sections[13] \"3.1. 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