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pmid:38665551

Identification of exosome-related gene signature as a promising diagnostic and therapeutic tool for breast cancer.

Qitong Chen · Qin Zhou

Heliyon · 2024 doi:10.1016/j.heliyon.2024.e29551

Paper

complete

Experiment

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Data

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Analysis

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Identification of exosome-related gene signature as a promising diagnostic and therapeutic tool for breast cancer.
doi
10.1016/j.heliyon.2024.e29551
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38665551
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Qitong Chen
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Qin Zhou
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Heliyon
year
2024
abstract
Background: Exosomes are promising tools for the development of new diagnostic and therapeutic approaches. Exosomes possess the ability to activate signaling pathways that contribute to the remodeling of the tumor microenvironment, angiogenesis, and the regulation of immune responses. We aimed to develop a prognostic score based on exosomes derived from breast cancer. Materials and methods: Training was conducted on the TCGA-BRCA dataset, while validation was conducted on GSE20685, GSE5764, GSE7904, and GSE29431. A total of 121 genes related to exosomes were retrieved from the ExoBCD database. The Cox proportional hazards model is used to develop risk score model. The GSVA package was utilized to analyze single-sample gene sets and identify exosome signatures, while the WGCNA package was utilized to identify gene modules associated with clinical outcomes. The clusterProfiler and GSVA R packages facilitated gene set enrichment and variation analyses. Furthermore, CIBERSORT quantified immune infiltration, and a correlation between gene expression and drug sensitivity was assessed using the TIDE algorithm. Results: An exosome-related prognostic score was established using the following selected genes: ABCC9, PIGR, CXCL13, DOK7, CD24, and IVL. Various immune cells that promote cancer immune evasion were associated with a high-risk prognostic score, which was an independent predictor of outcome. High-risk and low-risk groups exhibited significantly different infiltration abundances (p < 0.05). By conducting a sensitivity comparison, we found that patients with high-risk scores exhibited more favorable responses to immunotherapy than those with low-risk scores. Conclusion: The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.
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The Cox proportional hazards model is used to develop risk score model.
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The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.
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The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.
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The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.
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The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.
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The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.
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[3]
GSM134588
[4]
GSM134589
[5]
GSM134591
[6]
GSM134687
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GSM134688
[8]
GSM134689
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GSM134690
[10]
GSM134691
[11]
GSM134692
[12]
GSM134693
[13]
GSM134694
[14]
GSM134695
[15]
GSM134696
[16]
GSM134697
[17]
GSM134698
[18]
GSM134699
[19]
GSM134700
[20]
GSM134701
[21]
GSM134702
[22]
GSM134703
[23]
GSM134704
[24]
GSM134705
[25]
GSM134706
[26]
GSM134707
[27]
GSM134708
[28]
GSM134709
[29]
GSM134710
sample_count
30
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Analysis of microdissected invasive lobular and ductal breast carcinomas in relation to normal ductal and lobular cells
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[4] object · 15 fields
id
data:geo:GSE7904
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=GSE7904
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE7904
version
null
note
The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.
access_statement_kind
data_availability_statement
sample_accessions array · 62 items
[0]
GSM194397
[1]
GSM194398
[2]
GSM194399
[3]
GSM194400
[4]
GSM194401
[5]
GSM194402
[6]
GSM194403
[7]
GSM194404
[8]
GSM194405
[9]
GSM194406
[10]
GSM194407
[11]
GSM194408
[12]
GSM194409
[13]
GSM194410
[14]
GSM194411
[15]
GSM194412
[16]
GSM194413
[17]
GSM194414
[18]
GSM194415
[19]
GSM194416
[20]
GSM194417
[21]
GSM194418
[22]
GSM194419
[23]
GSM194420
[24]
GSM194421
[25]
GSM194422
[26]
GSM194423
[27]
GSM194424
[28]
GSM194425
[29]
GSM194426
[30]
GSM194427
[31]
GSM194428
[32]
GSM194429
[33]
GSM194430
[34]
GSM194431
[35]
GSM194432
[36]
GSM194433
[37]
GSM194434
[38]
GSM194435
[39]
GSM194436
[40]
GSM194437
[41]
GSM194438
[42]
GSM194439
[43]
GSM194440
[44]
GSM194441
[45]
GSM194442
[46]
GSM194443
[47]
GSM194444
[48]
GSM194445
[49]
GSM194446
[50]
GSM194447
[51]
GSM194448
[52]
GSM194449
[53]
GSM194450
[54]
GSM194451
[55]
GSM194452
[56]
GSM194453
[57]
GSM194454
[58]
GSM194455
[59]
GSM194456
[60]
GSM194457
[61]
GSM194458
sample_count
62
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Expression data from human breast tissue
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 8 items
[0]
asset:data:geo:GSE20685 not downloaded
[1]
asset:data:geo:GSE20685 licence not read
[2]
asset:data:geo:GSE29431 not downloaded
[3]
asset:data:geo:GSE29431 licence not read
[4]
asset:data:geo:GSE5764 not downloaded
[5]
asset:data:geo:GSE5764 licence not read
[6]
asset:data:geo:GSE7904 not downloaded
[7]
asset:data:geo:GSE7904 licence not read
analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
dsl_operations array · 1 item
[0]
cox_ph
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
band
verbatim
quote
The Cox proportional hazards model is used to develop risk score model.
[1] object · 10 fields
id
method-2
family
group_comparison
specific
student_t_test
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
student_t
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
Student's t-test
[2] object · 10 fields
id
method-3
family
group_comparison
specific
mann_whitney
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_mann_whitney
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
Mann-Whitney
[3] object · 10 fields
id
method-4
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
band
high
quote
Kaplan-Meier
[4] object · 10 fields
id
method-5
family
survival_analysis
specific
log_rank_test
label
Survival analysis
dsl_operations array · 1 item
[0]
logrank_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
band
high
quote
log-rank
[5] object · 10 fields
id
method-6
family
correlation_analysis
specific
pearson
label
Correlation analysis
dsl_operations array · 1 item
[0]
pearson_r
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
score
0.8
band
high
quote
Pearson correlation
[6] object · 10 fields
id
method-7
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
dsl_operations array · 1 item
[0]
chi_square_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
categorical_cross_tabulation
evidence object · 3 fields
score
0.8
band
high
quote
chi-square
[7] object · 10 fields
id
method-8
family
contingency_analysis
specific
fisher_exact
label
Categorical (contingency table) analysis
dsl_operations array · 2 items
[0]
contingency_table
[1]
chi_square_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
categorical_cross_tabulation
evidence object · 3 fields
score
0.8
band
high
quote
Fisher's exact
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gaps array · 1 item
[0]
method.reader_differs_from_extractor
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
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true
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cox_ph
missing_operations array · 0 items
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
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
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true
accessions array · 4 items
[0]
GSE20685
[1]
GSE5764
[2]
GSE7904
[3]
GSE29431
resolved_accessions array · 4 items
[0]
GSE20685
[1]
GSE5764
[2]
GSE7904
[3]
GSE29431
statements array · 1 item
[0]
The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.
basis
The paper names GSE20685, GSE5764, GSE7904, GSE29431 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 · 1 item
[0]
cox_ph
assets array · 2 items
[0]
source:pmid:38665551
[1]
data:geo:GSE20685
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE20685
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
2026-11-01T19:16:58Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
15244
completion_tokens
2094
cached_tokens
188
stages array · 1 item
[0] object · 4 fields
id
extraction
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complete
reader
MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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review.machine_critique
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review.human_critique
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absent
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not_run
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null
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gaps array · 1 item
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execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:38665551
type
paper
label
pmid:38665551
[1] object · 3 fields
id
source:pmid:38665551
type
manuscript
label
PMID 38665551 full text
[2] object · 3 fields
id
data:geo:GSE20685
type
dataset
label
GEO GSE20685
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:38665551
type
paper
label
pmid:38665551
[1] object · 3 fields
id
source:pmid:38665551
type
manuscript
label
PMID 38665551 full text
[2] object · 3 fields
id
data:geo:GSE20685
type
dataset
label
GEO GSE20685
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agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-38665551
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extraction
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[0]
source:pmid:38665551
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE20685
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accession_resolution
used array · 1 item
[0]
data:geo:GSE20685
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agent:corpus-assay-engine
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[0] object · 3 fields
id
agent:corpus-assay-engine
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software
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Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
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MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
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ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:38665551
parent_hash
sha256:e79263a93530cfa1405bb3aac15983c5dc3c1037de6c1ec6e6b3882f2a8e44b8
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null
gaps array · 13 items
[0]
asset:data:geo:GSE20685 licence not read
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[3]
asset:data:geo:GSE29431 not downloaded
[4]
asset:data:geo:GSE5764 licence not read
[5]
asset:data:geo:GSE5764 not downloaded
[6]
asset:data:geo:GSE7904 licence not read
[7]
asset:data:geo:GSE7904 not downloaded
[8]
execution.not_run
[9]
method.reader_differs_from_extractor
[10]
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[11]
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[12]
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[0] object · 11 fields
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analysis
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survival_analysis
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f2132e96ae6c7a4e
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cox_ph
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supported
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dsl_catalogue
f2132e96ae6c7a4e
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The Cox proportional hazards model is used to develop risk score model.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38665551", "kind": "science-record", "revision": 3, "content_hash": "sha256:80f13b4a2004f9d80cbdbbd72e9b9d8bcfe2ba81a6bfc4ebaa986d53986c9060", "created_at": "2026-11-01T19:20:38Z", "updated_at": "2026-11-01T22:11:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of exosome-related gene signature as a promising diagnostic and therapeutic tool for breast cancer.", "doi": "10.1016/j.heliyon.2024.e29551", "pmid": "38665551", "authors": ["Qitong Chen", "Qin Zhou"], "journal": "Heliyon", "year": 2024, "abstract": "Background: Exosomes are promising tools for the development of new diagnostic and therapeutic approaches. Exosomes possess the ability to activate signaling pathways that contribute to the remodeling of the tumor microenvironment, angiogenesis, and the regulation of immune responses. We aimed to develop a prognostic score based on exosomes derived from breast cancer.\nMaterials and methods: Training was conducted on the TCGA-BRCA dataset, while validation was conducted on GSE20685, GSE5764, GSE7904, and GSE29431. A total of 121 genes related to exosomes were retrieved from the ExoBCD database. The Cox proportional hazards model is used to develop risk score model. The GSVA package was utilized to analyze single-sample gene sets and identify exosome signatures, while the WGCNA package was utilized to identify gene modules associated with clinical outcomes. The clusterProfiler and GSVA R packages facilitated gene set enrichment and variation analyses. Furthermore, CIBERSORT quantified immune infiltration, and a correlation between gene expression and drug sensitivity was assessed using the TIDE algorithm.\nResults: An exosome-related prognostic score was established using the following selected genes: ABCC9, PIGR, CXCL13, DOK7, CD24, and IVL. Various immune cells that promote cancer immune evasion were associated with a high-risk prognostic score, which was an independent predictor of outcome. High-risk and low-risk groups exhibited significantly different infiltration abundances (p < 0.05). By conducting a sensitivity comparison, we found that patients with high-risk scores exhibited more favorable responses to immunotherapy than those with low-risk scores.\nConclusion: The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.", "claims": [{"id": "claim-method", "statement": "The Cox proportional hazards model is used to develop risk score model.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38665551", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "The Cox proportional hazards model is used to develop risk score model."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38665551", "locator": "sections[27] \"Data availability statement\" paragraph 2", "quote": "The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. Access to the TCGA-BRCA dataset can be obtained through the National Cancer Institute's Genomic Data Commons. GEO datasets are publicly available and can be accessed through the GEO repository by searching the respective accession numbers. These datasets were used under the terms of access provided by their respective repositories."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38665551", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The exosome-related gene signature exhibits outstanding performance in predicting the prognosis and cancer status of patients with breast cancer and guiding immunotherapy.", "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:38665551"], "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:GSE20685"], "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:GSE20685"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38665551", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.heliyon.2024.e29551", "sha256": "sha256:6e6313e8748f0a53378d59ac32514696bc1e03a49bc1a6dd3f94f0cf38bf4937", "bytes": 56748, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1016/j.heliyon.2024.e29551", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11043961", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE20685", "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=GSE20685", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE20685", "version": null, "note": "The Cancer Genome Atlas Breast Cancer (TCGA-BRCA) dataset, Gene Expression Omnibus (GEO) datasets GSE20685, GSE5764, GSE7904, and GSE29431. 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