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pmid:36865549

Novel exosome-related risk signature as prognostic biomarkers in glioblastoma.

Mingyan Ding · Qiang Xu · Xiuying Jin · Zhezhu Han · Hao Jiang · Honghua Sun · Yongmin Jin · Zhengri Piao · Songnan Zhang

Frontiers in immunology · 2023 doi:10.3389/fimmu.2023.1071023

Paper

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Experiment

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title
Novel exosome-related risk signature as prognostic biomarkers in glioblastoma.
doi
10.3389/fimmu.2023.1071023
pmid
36865549
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[0]
Mingyan Ding
[1]
Qiang Xu
[2]
Xiuying Jin
[3]
Zhezhu Han
[4]
Hao Jiang
[5]
Honghua Sun
[6]
Yongmin Jin
[7]
Zhengri Piao
[8]
Songnan Zhang
journal
Frontiers in immunology
year
2023
abstract
Exosomes are progressively being detected as an indicator for the diagnosis and prognosis of cancer in clinical settings. Many clinical trials have confirmed the impact of exosomes on tumor growth, particularly in anti-tumor immunity and immunosuppression of exosomes. Therefore, we developed a risk score based on genes found in glioblastoma-derived exosomes. In this study, we used the TCGA dataset as the training queue and GSE13041, GSE43378, GSE4412, and CGGA datasets as the external validation queue. Based on machine algorithms and bioinformatics methods, an exosome-generalized risk score was established. We found that the risk score could independently predict the prognosis of patients with glioma, and there were significant differences in the outcomes of patients in the high- and low-risk groups. Univariate and multivariate analyses showed that risk score is a valid predictive biomarker for gliomas. Two immunotherapy datasets, IMvigor210 and GSE78220, were obtained from previous studies. A high-risk score showed a significant association with multiple immunomodulators that could act on cancer immune evasion. The exosome-related risk score could predict the effectiveness of anti-PD-1 immunotherapy. Moreover, we compared the sensitivity of patients with high- and low-risk scores to various anti-cancer drugs and found that patients with high-risk scores had better responses to a variety of anti-cancer drugs. The risk-scoring model established in this study provides a useful tool to predict the total survival time of patients with glioma and guide immunotherapy.
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Lasso regression analysis was used to further reduce and validation the number of genes, and finally, three prognostic genes were screened, and a risk-scoring model was constructed ( Figures 2A, B ).
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Lasso regression analysis was used to further reduce and validation the number of genes, and finally, three prognostic genes were screened, and a risk-scoring model was constructed ( Figures 2A, B ).
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The exosome-related risk score independently predicted glioma prognosis and distinguished patients with significantly different outcomes in high- and low-risk groups.
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We found that the risk score could independently predict the prognosis of patients with glioma, and there were significant differences in the outcomes of patients in the high- and low-risk groups.
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The exosome-related risk score independently predicted glioma prognosis and distinguished patients with significantly different outcomes in high- and low-risk groups.
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licence_read
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[5] object · 15 fields
id
data:geo:SRP155030
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raw
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geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=SRP155030
sha256
null
bytes
null
access
open
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resolved
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null
reader_status
reader_required
identifier
SRP155030
version
null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
access_statement_kind
data_availability_statement
sample_accessions array · 0 items
sample_count
null
group_sizes
null
group_sizes_basis
null
platform
null
taxon
null
title
null
resolution_checked_at
2026-11-01T18:46:35Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 10 items
[0]
asset:data:geo:GSE106804 not downloaded
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asset:data:geo:GSE106804 licence not read
[2]
asset:data:geo:GSE13041 not downloaded
[3]
asset:data:geo:GSE13041 licence not read
[4]
asset:data:geo:GSE43378 not downloaded
[5]
asset:data:geo:GSE43378 licence not read
[6]
asset:data:geo:GSE78220 not downloaded
[7]
asset:data:geo:GSE78220 licence not read
[8]
asset:data:geo:SRP155030 not downloaded
[9]
asset:data:geo:SRP155030 licence not read
analysis object · 4 fields
state
partial
methods array · 2 items
[0] object · 10 fields
id
method-1
family
group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
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group_comparison_wilcoxon
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[1] object · 10 fields
id
method-2
family
null
specific
null
label
LASSO regression
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Lasso regression analysis was used to further reduce and validation the number of genes, and finally, three prognostic genes were screened, and a risk-scoring model was constructed ( Figures 2A, B ).
targets array · 0 items
gaps array · 2 items
[0]
method.reader_named_unmapped
[1]
method.group_comparison_wilcoxon
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
false
required_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: wilcoxon.
capability object · 4 fields
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 object · 6 fields
tier
R1
reachable
true
accessions array · 5 items
[0]
GSE106804
[1]
GSE13041
[2]
GSE43378
[3]
GSE78220
[4]
SRP155030
resolved_accessions array · 4 items
[0]
GSE106804
[1]
GSE13041
[2]
GSE43378
[3]
GSE78220
statements array · 1 item
[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
basis
The paper names GSE106804, GSE13041, GSE43378, GSE78220 in Gene-Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 0 items
assets array · 2 items
[0]
source:pmid:36865549
[1]
data:geo:GSE106804
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dsl_operations array · 1 item
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operation
group_comparison_wilcoxon
priority
null
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE106804
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:32:33Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
11995
completion_tokens
2752
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
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minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
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null
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gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
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id
pmid:36865549
type
paper
label
pmid:36865549
[1] object · 3 fields
id
source:pmid:36865549
type
manuscript
label
PMID 36865549 full text
[2] object · 3 fields
id
data:geo:GSE106804
type
dataset
label
GEO GSE106804
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:36865549
type
paper
label
pmid:36865549
[1] object · 3 fields
id
source:pmid:36865549
type
manuscript
label
PMID 36865549 full text
[2] object · 3 fields
id
data:geo:GSE106804
type
dataset
label
GEO GSE106804
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-36865549
type
extraction
used array · 1 item
[0]
source:pmid:36865549
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE106804
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE106804
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
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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
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snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:36865549
parent_hash
sha256:94159c0e12d6b29a6c74e2d210b95a7a22ec60f3d4fd3060902e0f613669f3a6
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null
gaps array · 17 items
[0]
asset:data:geo:GSE106804 licence not read
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[2]
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[3]
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[4]
asset:data:geo:GSE43378 licence not read
[5]
asset:data:geo:GSE43378 not downloaded
[6]
asset:data:geo:GSE78220 licence not read
[7]
asset:data:geo:GSE78220 not downloaded
[8]
asset:data:geo:SRP155030 licence not read
[9]
asset:data:geo:SRP155030 not downloaded
[10]
execution.not_run
[11]
method.group_comparison_wilcoxon
[12]
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[13]
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[14]
review.independent_reader
[15]
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[16]
step:run_analysis blocked on method:group_comparison_wilcoxon
assays array · 1 item
[0] object · 11 fields
role
analysis
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group_comparison
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dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36865549", "kind": "science-record", "revision": 3, "content_hash": "sha256:b6c64a60eb8f66292413d9d3a8c6a58ebc344333534a11be26636a3c1424ebdf", "created_at": "2026-11-01T19:01:30Z", "updated_at": "2026-11-01T22:08:58Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Novel exosome-related risk signature as prognostic biomarkers in glioblastoma.", "doi": "10.3389/fimmu.2023.1071023", "pmid": "36865549", "authors": ["Mingyan Ding", "Qiang Xu", "Xiuying Jin", "Zhezhu Han", "Hao Jiang", "Honghua Sun", "Yongmin Jin", "Zhengri Piao", "Songnan Zhang"], "journal": "Frontiers in immunology", "year": 2023, "abstract": "Exosomes are progressively being detected as an indicator for the diagnosis and prognosis of cancer in clinical settings. Many clinical trials have confirmed the impact of exosomes on tumor growth, particularly in anti-tumor immunity and immunosuppression of exosomes. Therefore, we developed a risk score based on genes found in glioblastoma-derived exosomes. In this study, we used the TCGA dataset as the training queue and GSE13041, GSE43378, GSE4412, and CGGA datasets as the external validation queue. Based on machine algorithms and bioinformatics methods, an exosome-generalized risk score was established. We found that the risk score could independently predict the prognosis of patients with glioma, and there were significant differences in the outcomes of patients in the high- and low-risk groups. Univariate and multivariate analyses showed that risk score is a valid predictive biomarker for gliomas. Two immunotherapy datasets, IMvigor210 and GSE78220, were obtained from previous studies. A high-risk score showed a significant association with multiple immunomodulators that could act on cancer immune evasion. The exosome-related risk score could predict the effectiveness of anti-PD-1 immunotherapy. Moreover, we compared the sensitivity of patients with high- and low-risk scores to various anti-cancer drugs and found that patients with high-risk scores had better responses to a variety of anti-cancer drugs. The risk-scoring model established in this study provides a useful tool to predict the total survival time of patients with glioma and guide immunotherapy.", "claims": [{"id": "claim-method", "statement": "Lasso regression analysis was used to further reduce and validation the number of genes, and finally, three prognostic genes were screened, and a risk-scoring model was constructed ( Figures 2A, B ).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36865549", "locator": "sections[12] \"Generation of prognostic gene signature and its functional annotation\" paragraph 2", "quote": "Lasso regression analysis was used to further reduce and validation the number of genes, and finally, three prognostic genes were screened, and a risk-scoring model was constructed ( Figures 2A, B )."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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