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pmid:35000592

Comprehensive analysis of a TNF family based-signature in diffuse gliomas with regard to prognosis and immune significance.

Qiang-Wei Wang · Wei-Wei Lin · Yong-Jian Zhu

Cell communication and signaling : CCS · 2022 doi:10.1186/s12964-021-00814-y

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Comprehensive analysis of a TNF family based-signature in diffuse gliomas with regard to prognosis and immune significance.
doi
10.1186/s12964-021-00814-y
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35000592
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[0]
Qiang-Wei Wang
[1]
Wei-Wei Lin
[2]
Yong-Jian Zhu
journal
Cell communication and signaling : CCS
year
2022
abstract
BACKGROUND: Several studies have shown that members of the tumor necrosis factor (TNF) family play an important role in cancer immunoregulation, and trials targeting these molecules are already underway. Our study aimed to integrate and analyze the expression patterns and clinical significance of TNF family-related genes in gliomas. METHODS: A total of 1749 gliomas from 4 datasets were enrolled in our study, including the Cancer Genome Atlas (TCGA) dataset as the training cohort and the other three datasets (CGGA, GSE16011, and Rembrandt) as validation cohorts. Clinical information, RNA expression data, and genomic profile were collected for analysis. We screened the signature gene set by Cox proportional hazards modelling. We evaluated the prognostic value of the signature by Kaplan-Meier analysis and timeROC curve. Gene Ontology (GO) and Gene set enrichment analysis (GSEA) analysis were performed for functional annotation. CIBERSORT algorithm and inflammatory metagenes were used to reveal immune characteristics. RESULTS: In gliomas, the expression of most TNF family members was positively correlated. Univariate analysis showed that most TNF family members were related to the overall survival of patients. Then through the LASSO regression model, we developed a TNF family-based signature, which was related to clinical, molecular, and genetic characteristics of patients with glioma. Moreover, the signature was found to be an independent prognostic marker through survival curve analysis and Cox regression analysis. Furthermore, a nomogram prognostic model was constructed to predict individual survival rates at 1, 3 and 5 years. Functional annotation analysis revealed that the immune and inflammatory response pathways were enriched in the high-risk group. Immunological analysis showed the immunosuppressive status in the high-risk group. CONCLUSIONS: We developed a TNF family-based signature to predict the prognosis of patients with glioma. Video abstract.
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By LASSO regression algorithm, we screened eight genes as covariates to evaluate prognostic value (Fig. 1a).
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sections[10] "Identification of a TNF family based-signature in gliomas" paragraph 2
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By LASSO regression algorithm, we screened eight genes as covariates to evaluate prognostic value (Fig. 1a).
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The authors confirm the data that has been used in this work is available on reasonable request.
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We developed a TNF family-based signature to predict the prognosis of patients with glioma.
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We developed a TNF family-based signature to predict the prognosis of patients with glioma.
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We developed a TNF family-based signature to predict the prognosis of patients with glioma.
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null
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570
taxon
Homo sapiens
title
The REMBRANDT study – a large collection of genomic data from brain cancer patients [gene expression]
resolution_checked_at
2026-11-01T17:30:42Z
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identifier_resolution_only_no_download_no_licence_read
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false
licence_read
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[2] object · 15 fields
id
data:geo:GSE16011
role
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geo-series
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE16011
sha256
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resolved
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identifier
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null
note
The authors confirm the data that has been used in this work is available on reasonable request.
structure object · 15 fields
repository
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GEO accession URL
access_statement_verbatim
The authors confirm the data that has been used in this work is available on reasonable request.
access_statement_kind
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sample_count
284
group_sizes
null
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null
platform
8542
taxon
Homo sapiens
title
Intrinsic Gene Expression Profiles of Gliomas are a Better Predictor of Survival than Histology
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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[0]
asset:data:geo:GSE108474 not downloaded
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[2]
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state
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[0] object · 10 fields
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By LASSO regression algorithm, we screened eight genes as covariates to evaluate prognostic value (Fig. 1a).
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time_to_event_with_censoring
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candidate
Automated Assays Laravel application and simulated adapters
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cox_ph
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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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owned
basis
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data object · 6 fields
tier
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reachable
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[0]
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[0]
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[0]
The authors confirm the data that has been used in this work is available on reasonable request.
basis
The paper names GSE16011, GSE108474 in GSE16011 and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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source:pmid:35000592
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minimax
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minimax
read_at
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[6]
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supported
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f2132e96ae6c7a4e
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[0]
By LASSO regression algorithm, we screened eight genes as covariates to evaluate prognostic value (Fig. 1a).
order_basis
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35000592", "kind": "science-record", "revision": 4, "content_hash": "sha256:3e0daef507432c5c21090a745fba2d8bc98c494ee52e95e45f6d0c88f2752b43", "created_at": "2026-11-01T17:36:43Z", "updated_at": "2026-11-01T22:05:32Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive analysis of a TNF family based-signature in diffuse gliomas with regard to prognosis and immune significance.", "doi": "10.1186/s12964-021-00814-y", "pmid": "35000592", "authors": ["Qiang-Wei Wang", "Wei-Wei Lin", "Yong-Jian Zhu"], "journal": "Cell communication and signaling : CCS", "year": 2022, "abstract": "BACKGROUND: Several studies have shown that members of the tumor necrosis factor (TNF) family play an important role in cancer immunoregulation, and trials targeting these molecules are already underway. Our study aimed to integrate and analyze the expression patterns and clinical significance of TNF family-related genes in gliomas.\nMETHODS: A total of 1749 gliomas from 4 datasets were enrolled in our study, including the Cancer Genome Atlas (TCGA) dataset as the training cohort and the other three datasets (CGGA, GSE16011, and Rembrandt) as validation cohorts. Clinical information, RNA expression data, and genomic profile were collected for analysis. We screened the signature gene set by Cox proportional hazards modelling. We evaluated the prognostic value of the signature by Kaplan-Meier analysis and timeROC curve. Gene Ontology (GO) and Gene set enrichment analysis (GSEA) analysis were performed for functional annotation. CIBERSORT algorithm and inflammatory metagenes were used to reveal immune characteristics.\nRESULTS: In gliomas, the expression of most TNF family members was positively correlated. Univariate analysis showed that most TNF family members were related to the overall survival of patients. Then through the LASSO regression model, we developed a TNF family-based signature, which was related to clinical, molecular, and genetic characteristics of patients with glioma. Moreover, the signature was found to be an independent prognostic marker through survival curve analysis and Cox regression analysis. Furthermore, a nomogram prognostic model was constructed to predict individual survival rates at 1, 3 and 5 years. Functional annotation analysis revealed that the immune and inflammatory response pathways were enriched in the high-risk group. Immunological analysis showed the immunosuppressive status in the high-risk group.\nCONCLUSIONS: We developed a TNF family-based signature to predict the prognosis of patients with glioma. 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