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pmid:39103477

Comprehensive analysis of sialylation-related genes and construct the prognostic model in sepsis.

Linfeng Tao · Yanyou Zhou · Lifang Wu · Jun Liu

Scientific reports · 2024 doi:10.1038/s41598-024-69185-x

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complete

Experiment

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Data

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title
Comprehensive analysis of sialylation-related genes and construct the prognostic model in sepsis.
doi
10.1038/s41598-024-69185-x
pmid
39103477
authors array · 4 items
[0]
Linfeng Tao
[1]
Yanyou Zhou
[2]
Lifang Wu
[3]
Jun Liu
journal
Scientific reports
year
2024
abstract
Sepsis, a life-threatening syndrome, continues to be a significant public health issue worldwide. Sialylation is a hot potential marker that affects the surface of a variety of cells. However, the role of genes related to sialylation and sepsis has not been fully explored. Bulk RNA-seq data sets (GSE66099 and GSE65682) were obtained from the open-access databases GEO. The classification of sepsis samples into subtypes was achieved by employing the R package "ConsensusClusterPlus" on the bulk RNA-seq data. Hub genes were discerned through the application of the R package "limma" and univariate regression analysis, with the calculation of risk scores carried out using the R package "survminer". To identify the best learning method and construct a prognostic model, we used 21 different combinations of machine learning, and C-index ranking results of these combinations have been showed. ROC curves, time-dependent ROC curves, and Kaplan-Meier curves were utilized to evaluate the diagnostic accuracy of the model. The R packages "ESTIMATE" and "GSVA" were employed to quantify the fractions of immune cell infiltration in each sample. The bulk RNA-seq samples were categorized into two distinct sepsis subtypes utilizing 14 prognosis-related sialylation genes. A total of 20 differentially expressed genes (DEGs) were identified as being associated with the relationship between sepsis and sialylation. The RSF was used to identify key genes with importance scores higher than 0.01. The nine hub genes (SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA) with the importance values greater than 0.01 was selected for constructing the prognostic model. This research offers some understanding of the relationship between sepsis and sialylation. Besides, it contains one predictive model that might develop into diagnostic biomarkers for sepsis.
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Finally, the RSF, which showed the highest C-index, was used to identify key genes with importance scores higher than 0.01 to develop a prognostic model.
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sections[6] "Establishment and validation of a prognostic model based on the prognostic genes in sepsis" paragraph 2
quote
Finally, the RSF, which showed the highest C-index, was used to identify key genes with importance scores higher than 0.01 to develop a prognostic model.
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The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
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sections[23] "notes" paragraph 1
quote
The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
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The RSF-based model identified nine hub genes with an importance value greater than 0.01: SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA.
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sections[13] "Construction of a prognostic model for sepsis" paragraph 2
quote
We ranked genes based on their importance (Fig. 9B) and identified nine hub genes (SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA) with an importance value greater than 0.01.
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The RSF-based model identified nine hub genes with an importance value greater than 0.01: SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA.
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The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
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[678]
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[692]
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[713]
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[714]
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[715]
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[718]
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[721]
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[786]
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[801]
GSM1692504
sample_count
802
group_sizes
null
group_sizes_basis
null
platform
13667
taxon
Homo sapiens
title
Genome-wide blood transcriptional profiling in critically ill patients - MARS consortium
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[2] object · 15 fields
id
data:geo:GSE66099
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=GSE66099
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE66099
version
null
note
The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
access_statement_kind
data_availability_statement
sample_accessions array · 276 items
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[1]
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[2]
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[8]
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[10]
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[11]
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[46]
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[47]
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[70]
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[268]
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[271]
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[274]
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[275]
GSM1617767
sample_count
276
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Unique Patients from the Genomics of Pediatric SIRS and Septic Shock Investigators (GPSSSI)
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 · 4 items
[0]
asset:data:geo:GSE65682 not downloaded
[1]
asset:data:geo:GSE65682 licence not read
[2]
asset:data:geo:GSE66099 not downloaded
[3]
asset:data:geo:GSE66099 licence not read
analysis object · 4 fields
state
partial
methods array · 4 items
[0] object · 10 fields
id
method-1
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
0.7
band
medium
quote
Kaplan-Meier
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method-2
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differential_expression
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limma_voom
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Differential expression analysis
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normalise_counts
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count_matrix_with_condition
evidence object · 3 fields
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0.7
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quote
limma
[2] object · 10 fields
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method-3
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network_analysis
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pathway_enrichment
label
Network / pathway analysis
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pathway_enrich
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edge_list
evidence object · 3 fields
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0.8
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high
quote
pathway enrichment
[3] object · 10 fields
id
method-4
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null
specific
null
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Random survival forest (RSF)
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missing_operations array · 0 items
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evidence object · 3 fields
score
1
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verbatim
quote
Finally, the RSF, which showed the highest C-index, was used to identify key genes with importance scores higher than 0.01 to develop a prognostic model.
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gaps array · 1 item
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method.reader_named_unmapped
capability object · 3 fields
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complete
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capability:computational_analysis
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Computational analysis platform
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[4]
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[5]
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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complete
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R1
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survival_km
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
capability object · 4 fields
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R1
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capability:computational_analysis
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owned
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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R1
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GSE66099
[1]
GSE65682
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[0]
GSE66099
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GSE65682
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[0]
The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.
basis
The paper names GSE66099, GSE65682 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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survival_km
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source:pmid:39103477
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data:geo:GSE65682
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review object · 5 fields
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partial
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extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
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2026-11-01T19:26:21Z
independence
single_reader
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verbatim
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verbatim
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5
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pmid:39103477
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paper
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pmid:39103477
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source:pmid:39103477
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manuscript
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PMID 39103477 full text
[2] object · 3 fields
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data:geo:GSE65682
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dataset
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GEO GSE65682
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activity-reading-sci-2026-11-01
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classification
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paper
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pmid:39103477
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source:pmid:39103477
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manuscript
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PMID 39103477 full text
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data:geo:GSE65682
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dataset
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GEO GSE65682
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agent:corpus-assay-engine
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activity-read-39103477
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extraction
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agent:minimax-reader
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used array · 1 item
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data:geo:GSE65682
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agent:corpus-assay-engine
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agent:minimax-reader
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MiniMax literature reader
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343fb30756ba6ec3
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lineage object · 4 fields
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99e1195c7d6f
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99e1195c7d6f
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[0]
and sepsis has not been fully explored. Bulk RNA-seq data sets (GSE66099 and GSE65682) were obtai
[1]
R package "ConsensusClusterPlus" on the bulk RNA-seq data. Hub genes were discerned through the a
[2]
e cell infiltration in each sample. The bulk RNA-seq samples were categorized into two distinct s
order_basis
paper_text_order:332
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assay:1
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39103477", "kind": "science-record", "revision": 3, "content_hash": "sha256:8e9142d1279b4ccedb7cf92a35b1dc1af3731916ab5c775f34a3585b26c43dfd", "created_at": "2026-11-01T20:29:10Z", "updated_at": "2026-11-01T22:12:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive analysis of sialylation-related genes and construct the prognostic model in sepsis.", "doi": "10.1038/s41598-024-69185-x", "pmid": "39103477", "authors": ["Linfeng Tao", "Yanyou Zhou", "Lifang Wu", "Jun Liu"], "journal": "Scientific reports", "year": 2024, "abstract": "Sepsis, a life-threatening syndrome, continues to be a significant public health issue worldwide. Sialylation is a hot potential marker that affects the surface of a variety of cells. However, the role of genes related to sialylation and sepsis has not been fully explored. Bulk RNA-seq data sets (GSE66099 and GSE65682) were obtained from the open-access databases GEO. The classification of sepsis samples into subtypes was achieved by employing the R package \"ConsensusClusterPlus\" on the bulk RNA-seq data. Hub genes were discerned through the application of the R package \"limma\" and univariate regression analysis, with the calculation of risk scores carried out using the R package \"survminer\". To identify the best learning method and construct a prognostic model, we used 21 different combinations of machine learning, and C-index ranking results of these combinations have been showed. ROC curves, time-dependent ROC curves, and Kaplan-Meier curves were utilized to evaluate the diagnostic accuracy of the model. The R packages \"ESTIMATE\" and \"GSVA\" were employed to quantify the fractions of immune cell infiltration in each sample. The bulk RNA-seq samples were categorized into two distinct sepsis subtypes utilizing 14 prognosis-related sialylation genes. A total of 20 differentially expressed genes (DEGs) were identified as being associated with the relationship between sepsis and sialylation. The RSF was used to identify key genes with importance scores higher than 0.01. The nine hub genes (SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA) with the importance values greater than 0.01 was selected for constructing the prognostic model. This research offers some understanding of the relationship between sepsis and sialylation. Besides, it contains one predictive model that might develop into diagnostic biomarkers for sepsis.", "claims": [{"id": "claim-method", "statement": "Finally, the RSF, which showed the highest C-index, was used to identify key genes with importance scores higher than 0.01 to develop a prognostic model.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39103477", "locator": "sections[6] \"Establishment and validation of a prognostic model based on the prognostic genes in sepsis\" paragraph 2", "quote": "Finally, the RSF, which showed the highest C-index, was used to identify key genes with importance scores higher than 0.01 to develop a prognostic model."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39103477", "locator": "sections[23] \"notes\" paragraph 1", "quote": "The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The RSF-based model identified nine hub genes with an importance value greater than 0.01: SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39103477", "locator": "sections[13] \"Construction of a prognostic model for sepsis\" paragraph 2", "quote": "We ranked genes based on their importance (Fig. 9B) and identified nine hub genes (SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA) with an importance value greater than 0.01."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The RSF-based model identified nine hub genes with an importance value greater than 0.01: SLA2A1, TMCC2, TFRC, RHAG, FKBP1B, KLF1, PILRA, ARL4A, and GYPA.", "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:39103477"], "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. 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"group_sizes_basis": null, "platform": "570", "taxon": "Homo sapiens", "title": "Unique Patients from the Genomics of Pediatric SIRS and Septic Shock Investigators (GPSSSI)", "resolution_checked_at": "2026-11-01T15:39:55Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}], "gaps": ["asset:data:geo:GSE65682 not downloaded", "asset:data:geo:GSE65682 licence not read", "asset:data:geo:GSE66099 not downloaded", "asset:data:geo:GSE66099 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "kaplan_meier", "label": "Survival analysis", "dsl_operations": ["survival_km"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 0.7, "band": "medium", "quote": "Kaplan-Meier"}}, {"id": "method-2", "family": "differential_expression", "specific": "limma_voom", "label": 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE66099", "GSE65682"], "resolved_accessions": ["GSE66099", "GSE65682"], "statements": ["The datasets (GSE66099 and GSE65682) for healthy and sepsis samples were acquired from the Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/) in this study."], "basis": "The paper names GSE66099, GSE65682 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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Bulk RNA-seq data sets (GSE66099 and GSE65682) were obtai", "R package \"ConsensusClusterPlus\" on the bulk RNA-seq data. Hub genes were discerned through the a", "e cell infiltration in each sample. The bulk RNA-seq samples were categorized into two distinct s"], "order_basis": "paper_text_order:332", "id": "assay:1"}, {"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["survival_km"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 0.7, "evidence": ["Kaplan-Meier"], "order_basis": "consumes_earlier_output", "id": "assay:2"}]}