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pmid:39739658

Identification of O-glycosylation related genes and subtypes in ulcerative colitis based on machine learning.

Yue Lu · Yi Su · Nan Wang · Dongyue Li · Huichao Zhang · Hongyu Xu

PloS one · 2024 doi:10.1371/journal.pone.0311495

Paper

complete

Experiment

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Data

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Analysis

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Execution

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title
Identification of O-glycosylation related genes and subtypes in ulcerative colitis based on machine learning.
doi
10.1371/journal.pone.0311495
pmid
39739658
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Yue Lu
[1]
Yi Su
[2]
Nan Wang
[3]
Dongyue Li
[4]
Huichao Zhang
[5]
Hongyu Xu
journal
PloS one
year
2024
abstract
Ulcerative colitis (UC) is an immune-related inflammatory bowel disease, with its underlying mechanisms being a central area of clinical research. O-GlcNAcylation plays a critical role in regulating immunity progression and the occurrence of inflammatory diseases and tumors. Yet, the mechanism of O-GlcNAc-associated colitis remains to be elucidated. To this end, the transcriptional and clinical data of GSE75214 and GSE92415 from the GEO database was hereby examined, and genes MUC1, ADAMTS1, GXYLT2, and SEMA5A were found to be significantly related to O-GlcNAcylation using machine learning methods. Based on the four hub genes, two UC subtypes were built. Notably, subtype B might be prone to developing colitis-associated colorectal cancer (CAC). This study delved into the role of intestinal glycosylation changes, especially the O-GlcNAcylation, and forged a foundation for further research on the occurrence and development of UC. Overall, understanding the role of O-GlcNAcylation in UC could have significant implications for diagnosis and treatment, offering valuable insights into the disease's progression.
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The genes that met the criteria of the adjusted P-value < 0.05 and |log fold change (FC)| > 1.0 or 0.5 were considered DEGs using the "limma" package.
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The genes that met the criteria of the adjusted P-value < 0.05 and |log fold change (FC)| > 1.0 or 0.5 were considered DEGs using the "limma" package.
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The study analyzed the transcriptional and clinical data of GSE75214 and GSE92415 from GEO and identified MUC1, ADAMTS1, GXYLT2, and SEMA5A as significantly related to O-GlcNAcylation using machine-learning methods.
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To this end, the transcriptional and clinical data of GSE75214 and GSE92415 from the GEO database was hereby examined, and genes MUC1, ADAMTS1, GXYLT2, and SEMA5A were found to be significantly related to O-GlcNAcylation using machine learning methods.
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The study analyzed the transcriptional and clinical data of GSE75214 and GSE92415 from GEO and identified MUC1, ADAMTS1, GXYLT2, and SEMA5A as significantly related to O-GlcNAcylation using machine-learning methods.
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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
true
required_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
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: limma_voom.
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 · 2 items
[0]
GSE75214
[1]
GSE92415
resolved_accessions array · 2 items
[0]
GSE75214
[1]
GSE92415
statements array · 1 item
[0]
The GSE75214 database contains intestinal mucosal biopsies obtained endoscopically from UC patients (n = 97) and healthy controls (n = 11), followed by microarray analysis to assess gene expression.
basis
The paper names GSE75214, GSE92415 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 · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
assets array · 2 items
[0]
source:pmid:39739658
[1]
data:geo:GSE75214
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:GSE75214
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
2026-11-01T19:43:38Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
null
calls
5
usage object · 3 fields
prompt_tokens
10980
completion_tokens
1176
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
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
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:39739658
type
paper
label
pmid:39739658
[1] object · 3 fields
id
source:pmid:39739658
type
manuscript
label
PMID 39739658 full text
[2] object · 3 fields
id
data:geo:GSE75214
type
dataset
label
GEO GSE75214
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:39739658
type
paper
label
pmid:39739658
[1] object · 3 fields
id
source:pmid:39739658
type
manuscript
label
PMID 39739658 full text
[2] object · 3 fields
id
data:geo:GSE75214
type
dataset
label
GEO GSE75214
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-39739658
type
extraction
used array · 1 item
[0]
source:pmid:39739658
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE75214
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE75214
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:39739658
parent_hash
sha256:9aeb2615638d6b028bee27e64dad95f6748f61ebe324bcc1b38b1f25a613412d
fork_of
null
gaps array · 9 items
[0]
asset:data:geo:GSE75214 licence not read
[1]
asset:data:geo:GSE75214 not downloaded
[2]
asset:data:geo:GSE92415 licence not read
[3]
asset:data:geo:GSE92415 not downloaded
[4]
execution.not_run
[5]
method.reader_differs_from_extractor
[6]
review.human_critique
[7]
review.independent_reader
[8]
review.machine_critique
assays array · 2 items
[0] object · 11 fields
role
data_generation
definition_id
microarray
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 2 items
[0]
(www.ncbi.nlm.nih.gov/geo/) retrieval of UC microarray datawere included: a) data from the same seq
[1]
) and healthy controls (n = 11), followed by microarray analysis to assess gene expression. GSE92415
order_basis
paper_text_order:1355
id
assay:1
[1] object · 11 fields
role
analysis
definition_id
differential_expression
definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
The genes that met the criteria of the adjusted P-value < 0.05 and |log fold change (FC)| > 1.0 or 0.5 were considered DEGs using the "limma" package.
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39739658", "kind": "science-record", "revision": 4, "content_hash": "sha256:5c3e10a722a88394cb25bb1c8ec12d688239ac5945f5c19588a03d3f5cc9d02c", "created_at": "2026-11-01T20:30:03Z", "updated_at": "2026-11-01T22:55:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of O-glycosylation related genes and subtypes in ulcerative colitis based on machine learning.", "doi": "10.1371/journal.pone.0311495", "pmid": "39739658", "authors": ["Yue Lu", "Yi Su", "Nan Wang", "Dongyue Li", "Huichao Zhang", "Hongyu Xu"], "journal": "PloS one", "year": 2024, "abstract": "Ulcerative colitis (UC) is an immune-related inflammatory bowel disease, with its underlying mechanisms being a central area of clinical research. O-GlcNAcylation plays a critical role in regulating immunity progression and the occurrence of inflammatory diseases and tumors. Yet, the mechanism of O-GlcNAc-associated colitis remains to be elucidated. To this end, the transcriptional and clinical data of GSE75214 and GSE92415 from the GEO database was hereby examined, and genes MUC1, ADAMTS1, GXYLT2, and SEMA5A were found to be significantly related to O-GlcNAcylation using machine learning methods. Based on the four hub genes, two UC subtypes were built. Notably, subtype B might be prone to developing colitis-associated colorectal cancer (CAC). This study delved into the role of intestinal glycosylation changes, especially the O-GlcNAcylation, and forged a foundation for further research on the occurrence and development of UC. Overall, understanding the role of O-GlcNAcylation in UC could have significant implications for diagnosis and treatment, offering valuable insights into the disease's progression.", "claims": [{"id": "claim-method", "statement": "The genes that met the criteria of the adjusted P-value < 0.05 and |log fold change (FC)| > 1.0 or 0.5 were considered DEGs using the \"limma\" package.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39739658", "locator": "sections[5] \"Identification of differential expressed genes\" paragraph 2", "quote": "The genes that met the criteria of the adjusted P-value < 0.05 and |log fold change (FC)| > 1.0 or 0.5 were considered DEGs using the \"limma\" package."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The GSE75214 database contains intestinal mucosal biopsies obtained endoscopically from UC patients (n = 97) and healthy controls (n = 11), followed by microarray analysis to assess gene expression.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39739658", "locator": "sections[3] \"Datasets and sample selection\" paragraph 2", "quote": "The GSE75214 database contains intestinal mucosal biopsies obtained endoscopically from UC patients (n = 97) and healthy controls (n = 11), followed by microarray analysis to assess gene expression."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study analyzed the transcriptional and clinical data of GSE75214 and GSE92415 from GEO and identified MUC1, ADAMTS1, GXYLT2, and SEMA5A as significantly related to O-GlcNAcylation using machine-learning methods.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39739658", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "To this end, the transcriptional and clinical data of GSE75214 and GSE92415 from the GEO database was hereby examined, and genes MUC1, ADAMTS1, GXYLT2, and SEMA5A were found to be significantly related to O-GlcNAcylation using machine learning methods."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study analyzed the transcriptional and clinical data of GSE75214 and GSE92415 from GEO and identified MUC1, ADAMTS1, GXYLT2, and SEMA5A as significantly related to O-GlcNAcylation using machine-learning methods.", "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:39739658"], "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:GSE75214"], "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:GSE75214"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39739658", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1371/journal.pone.0311495", "sha256": 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