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pmid:37292257

Focusing on scRNA-seq-Derived T Cell-Associated Genes to Identify Prognostic Signature and Immune Microenvironment Status in Low-Grade Glioma.

Jiayu Wen · Qiaoyi Huang · Jiuxiu Yao · Wei Wei · Zehui Li · Huiqin Zhang · Surui Chang · Hui Pei · Yu Cao · Hao Li

Mediators of inflammation · 2023 doi:10.1155/2023/3648946

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title
Focusing on scRNA-seq-Derived T Cell-Associated Genes to Identify Prognostic Signature and Immune Microenvironment Status in Low-Grade Glioma.
doi
10.1155/2023/3648946
pmid
37292257
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Jiayu Wen
[1]
Qiaoyi Huang
[2]
Jiuxiu Yao
[3]
Wei Wei
[4]
Zehui Li
[5]
Huiqin Zhang
[6]
Surui Chang
[7]
Hui Pei
[8]
Yu Cao
[9]
Hao Li
journal
Mediators of inflammation
year
2023
abstract
Background: The clinical outcomes of low-grade glioma (LGG) are associated with T cell infiltration, but the specific contribution of heterogeneous T cell types remains unclear. Method: To study the different functions of T cells in LGG, we mapped the single-cell RNA sequencing results of 10 LGG samples to obtain T cell marker genes. In addition, bulk RNA data of 975 LGG samples were collected for model construction. Algorithms such as TIMER, CIBERSORT, QUANTISEQ, MCPCOUTER, XCELL, and EPIC were used to depict the tumor microenvironment landscape. Subsequently, three immunotherapy cohorts, PRJEB23709, GSE78820, and IMvigor210, were used to explore the efficacy of immunotherapy. Results: The Human Primary Cell Atlas was used as a reference dataset to identify each cell cluster; a total of 15 cell clusters were defined and cells in cluster 12 were defined as T cells. According to the distribution of T cell subsets (CD4+ T cell, CD8+ T cell, Naïve T cell, and Treg cell), we selected the differentially expressed genes. Among the CD4+ T cell subsets, we screened 3 T cell-related genes, and the rest were 28, 4, and 13, respectively. Subsequently, according to the T cell marker genes, we screened six genes for constructing the model, namely, RTN1, HERPUD1, MX1, SEC61G, HOPX, and CHI3L1. The ROC curve showed that the predictive ability of the prognostic model for 1, 3, and 5 years was 0.881, 0.817, and 0.749 in the TCGA cohort, respectively. In addition, we found that risk scores were positively correlated with immune infiltration and immune checkpoints. To this end, we obtained three immunotherapy cohorts to verify their predictive ability of immunotherapy effects and found that high-risk patients had better clinical effects of immunotherapy. Conclusion: This single-cell RNA sequencing combined with bulk RNA sequencing may elucidate the composition of the tumor microenvironment and pave the way for the treatment of low-grade gliomas.
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LASSO algorithm was used to reduce the correlation between T cell marker genes and play a role in defitting. Subsequently, the multivariate Cox regression analysis algorithm was used to assign the coefficient of each gene to construct the prognosis model of T cell marker genes, in which the TCGA cohort was used as the training group and the CGGA cohort was used as the validation group.
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sections[5] "2.3. Construction of the Prognostic Model of T Cell Marker Genes" paragraph 2
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LASSO algorithm was used to reduce the correlation between T cell marker genes and play a role in defitting. Subsequently, the multivariate Cox regression analysis algorithm was used to assign the coefficient of each gene to construct the prognosis model of T cell marker genes, in which the TCGA cohort was used as the training group and the CGGA cohort was used as the validation group.
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The ROC curve shows that the prediction ability of the prognostic model at 1, 3, and 5 years in the TCGA cohort is 0.881, 0.817, and 0.749, respectively, and the prediction ability at 1, 3, and 5 years in the CGGA cohort is 0.749, 0.751, and 0.734, respectively (Figures 3(g) and 3(h)).
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sections[11] "3.2. Prognostic Model" paragraph 4
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The ROC curve shows that the prediction ability of the prognostic model at 1, 3, and 5 years in the TCGA cohort is 0.881, 0.817, and 0.749, respectively, and the prediction ability at 1, 3, and 5 years in the CGGA cohort is 0.749, 0.751, and 0.734, respectively (Figures 3(g) and 3(h)).
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The ROC curve shows that the prediction ability of the prognostic model at 1, 3, and 5 years in the TCGA cohort is 0.881, 0.817, and 0.749, respectively, and the prediction ability at 1, 3, and 5 years in the CGGA cohort is 0.749, 0.751, and 0.734, respectively (Figures 3(g) and 3(h)).
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reference_standard_and_test
evidence object · 3 fields
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medium
quote
ROC curve
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capability object · 3 fields
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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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
R1
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capability:computational_analysis
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basis
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data object · 6 fields
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[0]
GSE138794
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GSE16011
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PRJEB23709
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GSE78820
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GSE138794
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GSE16011
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GSE78820
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Data were obtained from CGGA, TCGA, and GEO, as detailed in the methodology section.
basis
The paper names GSE138794, GSE16011, GSE78820 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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dsl_operations array · 1 item
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cox_ph
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source:pmid:37292257
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data_gaps array · 1 item
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data:geo:GSE138794
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
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reader object · 5 fields
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MiniMax-M3.1-Flash
provider
minimax
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minimax
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independence
single_reader
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verbatim
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paper
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pmid:37292257
[1] object · 3 fields
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source:pmid:37292257
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manuscript
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PMID 37292257 full text
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data:geo:GSE138794
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GEO GSE138794
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pmid:37292257
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GEO GSE138794
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agent:corpus-assay-engine
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agent:minimax-reader
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Focusing on scRNA-seq-Derived T Cell-Associated Genes to Identify
[1]
t functions of T cells in LGG, we mapped the single-cell RNA sequencing results of 10 LGG samples to obtain T cell m
[2]
l effects of immunotherapy. Conclusion: This single-cell RNA sequencing combined with bulk RNA sequencing may elucid
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paper_text_order:0
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of T cells in LGG, we mapped the single-cell RNA sequencing results of 10 LGG samples to obtain T cell m
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immunotherapy. Conclusion: This single-cell RNA sequencing combined with bulk RNA sequencing may elucid
[2]
ingle-cell RNA sequencing combined with bulk RNA sequencing may elucidate the composition of the tumor m
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paper_text_order:362
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CIBERSORT, QUANTISEQ, MCPCOUTER, XCELL, and EPIC were used to depict the tumor microenvironme
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f2132e96ae6c7a4e
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LASSO algorithm was used to reduce the correlation between T cell marker genes and play a role in defitting. Subsequently, the multivariate Cox regression analysis algorithm was used to assign the coefficient of each gene to construct the prognosis model of T cell marker genes, in which the TCGA cohort was used as the training group and the CGGA cohort was used as the validation group.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37292257", "kind": "science-record", "revision": 3, "content_hash": "sha256:618504c0ada35ffe544e1eca18baf55a9d38b4ac8f9f20b56e74ad72d6062d5d", "created_at": "2026-11-01T19:02:01Z", "updated_at": "2026-11-01T22:09:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Focusing on scRNA-seq-Derived T Cell-Associated Genes to Identify Prognostic Signature and Immune Microenvironment Status in Low-Grade Glioma.", "doi": "10.1155/2023/3648946", "pmid": "37292257", "authors": ["Jiayu Wen", "Qiaoyi Huang", "Jiuxiu Yao", "Wei Wei", "Zehui Li", "Huiqin Zhang", "Surui Chang", "Hui Pei", "Yu Cao", "Hao Li"], "journal": "Mediators of inflammation", "year": 2023, "abstract": "Background: The clinical outcomes of low-grade glioma (LGG) are associated with T cell infiltration, but the specific contribution of heterogeneous T cell types remains unclear.\nMethod: To study the different functions of T cells in LGG, we mapped the single-cell RNA sequencing results of 10 LGG samples to obtain T cell marker genes. In addition, bulk RNA data of 975 LGG samples were collected for model construction. Algorithms such as TIMER, CIBERSORT, QUANTISEQ, MCPCOUTER, XCELL, and EPIC were used to depict the tumor microenvironment landscape. Subsequently, three immunotherapy cohorts, PRJEB23709, GSE78820, and IMvigor210, were used to explore the efficacy of immunotherapy.\nResults: The Human Primary Cell Atlas was used as a reference dataset to identify each cell cluster; a total of 15 cell clusters were defined and cells in cluster 12 were defined as T cells. According to the distribution of T cell subsets (CD4+ T cell, CD8+ T cell, Naïve T cell, and Treg cell), we selected the differentially expressed genes. Among the CD4+ T cell subsets, we screened 3 T cell-related genes, and the rest were 28, 4, and 13, respectively. Subsequently, according to the T cell marker genes, we screened six genes for constructing the model, namely, RTN1, HERPUD1, MX1, SEC61G, HOPX, and CHI3L1. The ROC curve showed that the predictive ability of the prognostic model for 1, 3, and 5 years was 0.881, 0.817, and 0.749 in the TCGA cohort, respectively. In addition, we found that risk scores were positively correlated with immune infiltration and immune checkpoints. To this end, we obtained three immunotherapy cohorts to verify their predictive ability of immunotherapy effects and found that high-risk patients had better clinical effects of immunotherapy.\nConclusion: This single-cell RNA sequencing combined with bulk RNA sequencing may elucidate the composition of the tumor microenvironment and pave the way for the treatment of low-grade gliomas.", "claims": [{"id": "claim-method", "statement": "LASSO algorithm was used to reduce the correlation between T cell marker genes and play a role in defitting. Subsequently, the multivariate Cox regression analysis algorithm was used to assign the coefficient of each gene to construct the prognosis model of T cell marker genes, in which the TCGA cohort was used as the training group and the CGGA cohort was used as the validation group.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37292257", "locator": "sections[5] \"2.3. Construction of the Prognostic Model of T Cell Marker Genes\" paragraph 2", "quote": "LASSO algorithm was used to reduce the correlation between T cell marker genes and play a role in defitting. Subsequently, the multivariate Cox regression analysis algorithm was used to assign the coefficient of each gene to construct the prognosis model of T cell marker genes, in which the TCGA cohort was used as the training group and the CGGA cohort was used as the validation group."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data were obtained from CGGA, TCGA, and GEO, as detailed in the methodology section.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37292257", "locator": "sections[16] \"Data Availability\" paragraph 2", "quote": "Data were obtained from CGGA, TCGA, and GEO, as detailed in the methodology section."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The ROC curve shows that the prediction ability of the prognostic model at 1, 3, and 5 years in the TCGA cohort is 0.881, 0.817, and 0.749, respectively, and the prediction ability at 1, 3, and 5 years in the CGGA cohort is 0.749, 0.751, and 0.734, respectively (Figures 3(g) and 3(h)).", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37292257", "locator": "sections[11] \"3.2. 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