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pmid:40860945

Identification and Experimental Validation of Oxidative Stress-Related Biomarkers in Ulcerative Colitis Using Machine Learning.

Siwei Duan · Qincheng Yi · Min Qiu · Zeming Zhu · Ziyi Zhang · Yong Gao · Dong Zhang

Journal of inflammation research · 2025 doi:10.2147/JIR.S520874

Paper

complete

Experiment

partial

Data

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Analysis

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Execution

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title
Identification and Experimental Validation of Oxidative Stress-Related Biomarkers in Ulcerative Colitis Using Machine Learning.
doi
10.2147/JIR.S520874
pmid
40860945
authors array · 7 items
[0]
Siwei Duan
[1]
Qincheng Yi
[2]
Min Qiu
[3]
Zeming Zhu
[4]
Ziyi Zhang
[5]
Yong Gao
[6]
Dong Zhang
journal
Journal of inflammation research
year
2025
abstract
Purpose: Ulcerative colitis (UC) remains challenging to diagnose and treat due to a lack of reliable biomarkers. This study investigates oxidative stress-related targets in UC using bioinformatics and experimental validation. Methods: We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification). An artificial neural network (ANN) diagnostic model was constructed, followed by chromosomal distribution analysis, immune infiltration assessment, and drug screening. Hub gene expression was validated in a 3% DSS-induced colitis mouse model via qPCR and Western blot. Results: Ultimately there were 6 hub genes identified: DUOX2, ETFDH, GPX8, ITGA5, NPY, and PDK2, which were validated with 3 other datasets. In the DSS-colitis model, DUOX2 and ITGA5 were significantly upregulated (p < 0.05), whereas ETFDH, PDK2, and NPY were downregulated. GPX8 protein expression was elevated in colonic mucosa compared to controls. These findings were further validated in three independent datasets (GSE48958, GSE16879, GSE36807). Conclusion: Our study identifies six oxidative stress-related biomarkers in UC using machine learning and experimental validation. These findings provide potential diagnostic and therapeutic targets for UC management, paving the way for further clinical investigations.
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We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification).
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We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification).
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The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
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Ultimately there were 6 hub genes identified: DUOX2, ETFDH, GPX8, ITGA5, NPY, and PDK2, which were validated with 3 other datasets.
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Ultimately there were 6 hub genes identified: DUOX2, ETFDH, GPX8, ITGA5, NPY, and PDK2, which were validated with 3 other datasets.
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Ultimately there were 6 hub genes identified: DUOX2, ETFDH, GPX8, ITGA5, NPY, and PDK2, which were validated with 3 other datasets.
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[115]
GSM1426186
sample_count
116
group_sizes
null
group_sizes_basis
null
platform
6244
taxon
Homo sapiens
title
Mucosal gene expression profiling in patients with inflammatory bowel disease
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[6] object · 15 fields
id
data:geo:GSE87465
role
raw
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geo-series
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application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE87465
sha256
null
bytes
null
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null
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GSE87465
version
null
note
The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
access_statement_kind
data_availability_statement
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GSM2332079
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GSM2332081
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GSM2332082
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GSM2332083
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GSM2332084
[6]
GSM2332085
[7]
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[8]
GSM2332087
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GSM2332088
[10]
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[11]
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[13]
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[14]
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[15]
GSM2332094
[16]
GSM2332095
[17]
GSM2332096
[18]
GSM2332097
sample_count
19
group_sizes
null
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null
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13158
taxon
Homo sapiens
title
Gene expression profiling of mucosal biopsies from pediatric patients with moderately to severely active ulcerative colitis
resolution_checked_at
2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[7] object · 15 fields
id
data:geo:GSE87466
role
raw
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geo-series
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application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE87466
sha256
null
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null
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resolved
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null
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reader_required
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GSE87466
version
null
note
The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 108 items
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GSM2332098
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[6]
GSM2332104
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[8]
GSM2332106
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GSM2332107
[10]
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GSM2332109
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GSM2332111
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[44]
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[46]
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[50]
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[53]
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[54]
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GSM2332205
sample_count
108
group_sizes
null
group_sizes_basis
null
platform
13158
taxon
Homo sapiens
title
Gene expression profiling of mucosal biopsies from adult patients with moderately to severely active ulcerative colitis
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 14 items
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asset:data:geo:GSE16879 not downloaded
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asset:data:geo:GSE36807 licence not read
[4]
asset:data:geo:GSE38713 not downloaded
[5]
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[6]
asset:data:geo:GSE48958 not downloaded
[7]
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[8]
asset:data:geo:GSE59071 not downloaded
[9]
asset:data:geo:GSE59071 licence not read
[10]
asset:data:geo:GSE87465 not downloaded
[11]
asset:data:geo:GSE87465 licence not read
[12]
asset:data:geo:GSE87466 not downloaded
[13]
asset:data:geo:GSE87466 licence not read
analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
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machine_learning
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random_forest
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missing_operations array · 1 item
[0]
machine_learning_random_forest
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labelled_feature_matrix
evidence object · 3 fields
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1
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quote
We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification).
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two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
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analysis of variance
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network_analysis
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Network / pathway analysis
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[0]
pathway_enrich
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parameters object · 0 fields
data_shapes array · 1 item
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edge_list
evidence object · 3 fields
score
0.8
band
high
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pathway enrichment
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gaps array · 2 items
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method.reader_differs_from_extractor
[1]
method.machine_learning_random_forest
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
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survival_analysis
[3]
statistical_regression
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differential_expression
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
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expressible
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missing_operations array · 1 item
[0]
machine_learning_random_forest
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: random_forest.
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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accessions array · 7 items
[0]
GSE38713
[1]
GSE59071
[2]
GSE87465
[3]
GSE87466
[4]
GSE48958
[5]
GSE16879
[6]
GSE36807
resolved_accessions array · 7 items
[0]
GSE38713
[1]
GSE59071
[2]
GSE87465
[3]
GSE87466
[4]
GSE48958
[5]
GSE16879
[6]
GSE36807
statements array · 1 item
[0]
The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). All raw data and code are available from the corresponding author Dong Zhang,with a reasonable request.
basis
The paper names GSE38713, GSE59071, GSE87465, GSE87466, GSE48958, GSE16879, GSE36807 in GEO database 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:40860945
[1]
data:geo:GSE16879
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[0] object · 3 fields
operation
machine_learning_random_forest
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null
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data_gaps array · 1 item
[0]
data:geo:GSE16879
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T20:00:37Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
usage object · 3 fields
prompt_tokens
17464
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1647
cached_tokens
264
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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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[2]
review.human_critique
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absent
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not_run
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null
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execution.not_run
provenance object · 7 fields
entities array · 3 items
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id
pmid:40860945
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paper
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pmid:40860945
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id
source:pmid:40860945
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manuscript
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PMID 40860945 full text
[2] object · 3 fields
id
data:geo:GSE16879
type
dataset
label
GEO GSE16879
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:40860945
type
paper
label
pmid:40860945
[1] object · 3 fields
id
source:pmid:40860945
type
manuscript
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PMID 40860945 full text
[2] object · 3 fields
id
data:geo:GSE16879
type
dataset
label
GEO GSE16879
agent
agent:corpus-assay-engine
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id
activity-read-40860945
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extraction
used array · 1 item
[0]
source:pmid:40860945
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE16879
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accession_resolution
used array · 1 item
[0]
data:geo:GSE16879
agent
agent:corpus-assay-engine
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id
agent:corpus-assay-engine
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id
agent:minimax-reader
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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:40860945
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sha256:3566d34a2ebbe01e41db9b51799bf5c98ad4eb04185879746af4b8f986d11eef
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null
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[1]
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[2]
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[3]
asset:data:geo:GSE36807 not downloaded
[4]
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[5]
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[6]
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[7]
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[10]
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[11]
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[12]
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[13]
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[14]
execution.not_run
[15]
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[16]
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[17]
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[18]
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[20]
step:run_analysis blocked on method:machine_learning_random_forest
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[0] object · 11 fields
role
data_generation
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animal_model
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99e1195c7d6f
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partial
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99e1195c7d6f
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[0]
on was validated in a 3% DSS-induced colitis mouse model via qPCR and Western blot. Results: Ultimate
[1]
on was validated in a 3% DSS-induced colitis mouse model via qPCR and Western blot. Results: Ul
[2]
e: SCXK (Guangdong) 002020–0051; China). The mice were housed in six cages (3–4 mice per cage) sett
[3]
rimental Validation Three groups of C57BL/6J mice were randomly assigned to a control group, a 3% D
order_basis
paper_text_order:749
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[1] object · 11 fields
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99e1195c7d6f
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in a 3% DSS-induced colitis mouse model via qPCR and Western blot. Results: Ultimately there
[1]
length in each group of mice (Unit: cm). (g) qPCR validation of hub genes. (h) Western blot va
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paper_text_order:766
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assay:2
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data_generation
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99e1195c7d6f
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99e1195c7d6f
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[0]
DSS-induced colitis mouse model via qPCR and Western blot. Results: Ultimately there were 6 hub genes
[1]
: cm). (g) qPCR validation of hub genes. (h) Western blot validation of hub genes. (In Figures d,e and
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paper_text_order:774
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[3] object · 11 fields
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machine_learning
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f2132e96ae6c7a4e
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f2132e96ae6c7a4e
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[0]
We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification).
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:40860945", "kind": "science-record", "revision": 3, "content_hash": "sha256:8e5f539ed6f7fd2b0aa0e963288c69ace54e39557fe56e1000f8892f44a50324", "created_at": "2026-11-01T20:30:59Z", "updated_at": "2026-11-01T22:14:38Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and Experimental Validation of Oxidative Stress-Related Biomarkers in Ulcerative Colitis Using Machine Learning.", "doi": "10.2147/JIR.S520874", "pmid": "40860945", "authors": ["Siwei Duan", "Qincheng Yi", "Min Qiu", "Zeming Zhu", "Ziyi Zhang", "Yong Gao", "Dong Zhang"], "journal": "Journal of inflammation research", "year": 2025, "abstract": "Purpose: Ulcerative colitis (UC) remains challenging to diagnose and treat due to a lack of reliable biomarkers. This study investigates oxidative stress-related targets in UC using bioinformatics and experimental validation.\nMethods: We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification). An artificial neural network (ANN) diagnostic model was constructed, followed by chromosomal distribution analysis, immune infiltration assessment, and drug screening. Hub gene expression was validated in a 3% DSS-induced colitis mouse model via qPCR and Western blot.\nResults: Ultimately there were 6 hub genes identified: DUOX2, ETFDH, GPX8, ITGA5, NPY, and PDK2, which were validated with 3 other datasets. In the DSS-colitis model, DUOX2 and ITGA5 were significantly upregulated (p < 0.05), whereas ETFDH, PDK2, and NPY were downregulated. GPX8 protein expression was elevated in colonic mucosa compared to controls. These findings were further validated in three independent datasets (GSE48958, GSE16879, GSE36807).\nConclusion: Our study identifies six oxidative stress-related biomarkers in UC using machine learning and experimental validation. These findings provide potential diagnostic and therapeutic targets for UC management, paving the way for further clinical investigations.", "claims": [{"id": "claim-method", "statement": "We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40860945", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "We analyzed four GEO datasets and oxidative-stress genes from MSigDB, applying differential analysis, LASSO regression (for feature selection), and random forest (for robust biomarker identification)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used in this study can be accessed through the GEO database (https://www.ncbi.nlm.nih.gov/geo/). 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