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pmid:36341390

Establishment and validation of a novel prognostic model for lower-grade glioma based on senescence-related genes.

Junsheng Li · Jia Wang · Dongjing Liu · Chuming Tao · Jizong Zhao · Wen Wang

Frontiers in immunology · 2022 doi:10.3389/fimmu.2022.1018942

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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title
Establishment and validation of a novel prognostic model for lower-grade glioma based on senescence-related genes.
doi
10.3389/fimmu.2022.1018942
pmid
36341390
authors array · 6 items
[0]
Junsheng Li
[1]
Jia Wang
[2]
Dongjing Liu
[3]
Chuming Tao
[4]
Jizong Zhao
[5]
Wen Wang
journal
Frontiers in immunology
year
2022
abstract
Objective: Increasing studies have indicated that senescence was associated with tumorigenesis and progression. Lower-grade glioma (LGG) presented a less invasive nature, however, its treatment efficacy and prognosis prediction remained challenging due to the intrinsic heterogeneity. Therefore, we established a senescence-related signature and investigated its prognostic role in LGGs. Methods: The gene expression data and clinicopathologic features were from The Cancer Genome Atlas (TCGA) database. The experimentally validated senescence genes (SnGs) from the CellAge database were obtained. Then LASSO regression has been performed to build a prognostic model. Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score. A nomogram model has been constructed for outcome prediction. Immunological analyses were further performed. Data from the Chinese Glioma Genome Atlas (CGGA), Repository of Molecular Brain Neoplasia Data (REMBRANDT), and GSE16011 were used for validation. Results: The 6-SnG signature has been established. The results showed SnG-risk score could be considered as an independent predictor for LGG patients (HR=2.763, 95%CI=1.660-4.599, P<0.001). The high SnG-risk score indicated a worse outcome in LGG (P<0.001). Immune analysis showed a positive correlation between the SnG-risk score and immune infiltration level, and the expression of immune checkpoints. The CGGA datasets confirmed the prognostic role of the SnG-risk score. And Kaplan-Meier analyses in the additional datasets (CGGA, REMBRANDT, and GSE16011) validated the prognostic role of the SnG-signature (P<0.001 for all). Conclusion: The SnG-related prognostic model could predict the survival of LGG accurately. This study proposed a novel indicator for predicting the prognosis of LGG and provided potential therapeutic targets.
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Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score.
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Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score.
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.
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The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).
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The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).
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sections[13] "Establishment of the SnG-related signature and evaluation of its prognostic role" paragraph 6
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The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).
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The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).
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title
Intrinsic Gene Expression Profiles of Gliomas are a Better Predictor of Survival than Histology
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agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
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 object · 4 fields
parent_id
pmid:36341390
parent_hash
sha256:6c2523523179c04b1f1596bbc21d7cc82c8503101298a155b75e3d6b00677aac
fork_of
null
gaps array · 6 items
[0]
asset:data:geo:GSE16011 licence not read
[1]
asset:data:geo:GSE16011 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]
Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score.
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:36341390", "kind": "science-record", "revision": 3, "content_hash": "sha256:68f4bc2260c65d02b5de86af3169e82bb928d1ca26dbeb0719842c045a3492e1", "created_at": "2026-11-01T18:15:47Z", "updated_at": "2026-11-01T21:29:24Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Establishment and validation of a novel prognostic model for lower-grade glioma based on senescence-related genes.", "doi": "10.3389/fimmu.2022.1018942", "pmid": "36341390", "authors": ["Junsheng Li", "Jia Wang", "Dongjing Liu", "Chuming Tao", "Jizong Zhao", "Wen Wang"], "journal": "Frontiers in immunology", "year": 2022, "abstract": "Objective: Increasing studies have indicated that senescence was associated with tumorigenesis and progression. Lower-grade glioma (LGG) presented a less invasive nature, however, its treatment efficacy and prognosis prediction remained challenging due to the intrinsic heterogeneity. Therefore, we established a senescence-related signature and investigated its prognostic role in LGGs.\nMethods: The gene expression data and clinicopathologic features were from The Cancer Genome Atlas (TCGA) database. The experimentally validated senescence genes (SnGs) from the CellAge database were obtained. Then LASSO regression has been performed to build a prognostic model. Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score. A nomogram model has been constructed for outcome prediction. Immunological analyses were further performed. Data from the Chinese Glioma Genome Atlas (CGGA), Repository of Molecular Brain Neoplasia Data (REMBRANDT), and GSE16011 were used for validation.\nResults: The 6-SnG signature has been established. The results showed SnG-risk score could be considered as an independent predictor for LGG patients (HR=2.763, 95%CI=1.660-4.599, P&lt;0.001). The high SnG-risk score indicated a worse outcome in LGG (P&lt;0.001). Immune analysis showed a positive correlation between the SnG-risk score and immune infiltration level, and the expression of immune checkpoints. The CGGA datasets confirmed the prognostic role of the SnG-risk score. And Kaplan-Meier analyses in the additional datasets (CGGA, REMBRANDT, and GSE16011) validated the prognostic role of the SnG-signature (P&lt;0.001 for all).\nConclusion: The SnG-related prognostic model could predict the survival of LGG accurately. This study proposed a novel indicator for predicting the prognosis of LGG and provided potential therapeutic targets.", "claims": [{"id": "claim-method", "statement": "Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36341390", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Cox regression and Kaplan-Meier survival curves were performed to investigate the prognostic value of the SnG-risk score."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36341390", "locator": "sections[21] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).", "kind": "quantitative", "target": {"value": 95.0, "unit": "per cent", "tolerance": null, "source": "The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 )."}, "evidence": [{"asset": "source:pmid:36341390", "locator": "sections[13] \"Establishment of the SnG-related signature and evaluation of its prognostic role\" paragraph 6", "quote": "The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 )."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The result of Cox regression showed that the SnG-risk score was an independent indicator for LGG survival (HR=2.763, 95%CI=1.660-4.599, P<0.001, Table 2 ).", "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:36341390"], "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:GSE16011"], "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:GSE16011"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36341390", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fimmu.2022.1018942", "sha256": "sha256:93c12a7270b238ecd43b77a7a0c357e3f69ff46feb048f553b58f3b3bd4b7757", "bytes": 41848, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fimmu.2022.1018942", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9633681", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE16011", "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=GSE16011", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE16011", "version": null, "note": "The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The original contributions presented in the study are included in the article/supplementary material. 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