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pmid:41607549

Unveiling the prognostic role of FABP4 in early-onset colorectal cancer through big data analysis and preliminary clinical validation.

Yu Wu · Weiwei Zou · Shengjun Zhang · Lipeng Zhao · Shaohua He · Fan Yao · Peilin Qing · Yixin Li · Jie Li · Xiao-Liang Xing

Frontiers in oncology · 2025 doi:10.3389/fonc.2025.1689952

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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pmid:41607549
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title
Unveiling the prognostic role of FABP4 in early-onset colorectal cancer through big data analysis and preliminary clinical validation.
doi
10.3389/fonc.2025.1689952
pmid
41607549
authors array · 10 items
[0]
Yu Wu
[1]
Weiwei Zou
[2]
Shengjun Zhang
[3]
Lipeng Zhao
[4]
Shaohua He
[5]
Fan Yao
[6]
Peilin Qing
[7]
Yixin Li
[8]
Jie Li
[9]
Xiao-Liang Xing
journal
Frontiers in oncology
year
2025
abstract
Background: Early-onset colorectal cancer (EOCRC), characterized by greater aggressiveness and advanced stage at diagnosis, is increasing globally. This study aimed to identify suitable prognostic biomarkers for EOCRC. Methods: Gene expression and clinical data from TCGA and GEO (GSE39582, GSE17536, and GSE17537) datasets were analyzed. Differential expression, univariate and multivariate Cox regression, and correlation analyses were performed. Immune status was evaluated using ESTIMATE and CONSENSUS TME algorithm. Immunotherapy and chemotherapy response was predicted via the TIDE and oncoPredict algorithm, respectively. Candidate signatures were validated in clinical samples from three EOCRC patients using qRT-PCR. Results: Fatty Acid Binding Protein 4 (FABP4) was identified as an independent prognostic factor for poor overall survival in EOCRC patients. A prognostic model based on FABP4 demonstrated good predictive accuracy for 1-, 3-, and 5-year survival in both training and validation sets. The high-FABP4 expression was negative correlated TIDE scores, suggesting EOCRC patients with high expression of FABP4 maybe benefit from immunotherapy. Furthermore, 66 chemotherapeutic agents showed significant negative correlations with FABP4 expression. Validation in patient samples confirmed the coordinated upregulation of FABP4 and its associated genes ADIPOQ and IGF1. Conclusion: FABP4 is a promising independent prognostic biomarker for EOCRC, associated with an immunosuppressive microenvironment and maybe a potential guidance for immunotherapy and chemotherapy selection. Further multi-center prospective studies are warranted to validate its clinical utility.
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Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS).
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Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS).
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The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.
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FABP4 was identified as an independent prognostic factor for poor overall survival in EOCRC patients.
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Fatty Acid Binding Protein 4 (FABP4) was identified as an independent prognostic factor for poor overall survival in EOCRC patients.
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FABP4 was identified as an independent prognostic factor for poor overall survival in EOCRC patients.
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Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients (Moffitt Samples)
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[228]
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[229]
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[413]
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[414]
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[417]
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[418]
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[420]
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[421]
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[422]
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[423]
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[424]
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[426]
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[474]
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[484]
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sample_count
585
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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gaps array · 6 items
[0]
asset:data:geo:GSE17536 not downloaded
[1]
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[2]
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[3]
asset:data:geo:GSE17537 licence not read
[4]
asset:data:geo:GSE39582 not downloaded
[5]
asset:data:geo:GSE39582 licence not read
analysis object · 4 fields
state
partial
methods array · 2 items
[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
Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS).
[1] object · 10 fields
id
method-2
family
group_comparison
specific
anova
label
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dsl_operations array · 4 items
[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
missing_operations array · 0 items
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
analysis of variance
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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]
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[3]
statistical_regression
[4]
pca
[5]
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[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 · 1 item
[0]
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
reachable
true
accessions array · 3 items
[0]
GSE39582
[1]
GSE17536
[2]
GSE17537
resolved_accessions array · 3 items
[0]
GSE39582
[1]
GSE17536
[2]
GSE17537
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.
basis
The paper names GSE39582, GSE17536, GSE17537 in 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:41607549
[1]
data:geo:GSE17536
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:GSE17536
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
2026-11-01T20:11:24Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
13502
completion_tokens
1224
cached_tokens
264
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
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[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:41607549
type
paper
label
pmid:41607549
[1] object · 3 fields
id
source:pmid:41607549
type
manuscript
label
PMID 41607549 full text
[2] object · 3 fields
id
data:geo:GSE17536
type
dataset
label
GEO GSE17536
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:41607549
type
paper
label
pmid:41607549
[1] object · 3 fields
id
source:pmid:41607549
type
manuscript
label
PMID 41607549 full text
[2] object · 3 fields
id
data:geo:GSE17536
type
dataset
label
GEO GSE17536
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-41607549
type
extraction
used array · 1 item
[0]
source:pmid:41607549
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE17536
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE17536
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
type
software
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MiniMax literature reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
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lineage object · 4 fields
parent_id
pmid:41607549
parent_hash
sha256:94c2bbd232de24bbde203a2574495198c4ada20ebdd4fe1c90c5a968a156b6a7
fork_of
null
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[0]
asset:data:geo:GSE17536 licence not read
[1]
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[2]
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[3]
asset:data:geo:GSE17537 not downloaded
[4]
asset:data:geo:GSE39582 licence not read
[5]
asset:data:geo:GSE39582 not downloaded
[6]
execution.not_run
[7]
method.reader_differs_from_extractor
[8]
review.human_critique
[9]
review.independent_reader
[10]
review.machine_critique
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[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS).
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41607549", "kind": "science-record", "revision": 3, "content_hash": "sha256:dc4f7292f7d1cdc81b23815fdba997f552590e7476bb9bdb1c40c2d468214eea", "created_at": "2026-11-01T20:31:34Z", "updated_at": "2026-11-01T22:15:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Unveiling the prognostic role of FABP4 in early-onset colorectal cancer through big data analysis and preliminary clinical validation.", "doi": "10.3389/fonc.2025.1689952", "pmid": "41607549", "authors": ["Yu Wu", "Weiwei Zou", "Shengjun Zhang", "Lipeng Zhao", "Shaohua He", "Fan Yao", "Peilin Qing", "Yixin Li", "Jie Li", "Xiao-Liang Xing"], "journal": "Frontiers in oncology", "year": 2025, "abstract": "Background: Early-onset colorectal cancer (EOCRC), characterized by greater aggressiveness and advanced stage at diagnosis, is increasing globally. This study aimed to identify suitable prognostic biomarkers for EOCRC.\nMethods: Gene expression and clinical data from TCGA and GEO (GSE39582, GSE17536, and GSE17537) datasets were analyzed. Differential expression, univariate and multivariate Cox regression, and correlation analyses were performed. Immune status was evaluated using ESTIMATE and CONSENSUS TME algorithm. Immunotherapy and chemotherapy response was predicted via the TIDE and oncoPredict algorithm, respectively. Candidate signatures were validated in clinical samples from three EOCRC patients using qRT-PCR.\nResults: Fatty Acid Binding Protein 4 (FABP4) was identified as an independent prognostic factor for poor overall survival in EOCRC patients. A prognostic model based on FABP4 demonstrated good predictive accuracy for 1-, 3-, and 5-year survival in both training and validation sets. The high-FABP4 expression was negative correlated TIDE scores, suggesting EOCRC patients with high expression of FABP4 maybe benefit from immunotherapy. Furthermore, 66 chemotherapeutic agents showed significant negative correlations with FABP4 expression. Validation in patient samples confirmed the coordinated upregulation of FABP4 and its associated genes ADIPOQ and IGF1.\nConclusion: FABP4 is a promising independent prognostic biomarker for EOCRC, associated with an immunosuppressive microenvironment and maybe a potential guidance for immunotherapy and chemotherapy selection. Further multi-center prospective studies are warranted to validate its clinical utility.", "claims": [{"id": "claim-method", "statement": "Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41607549", "locator": "sections[4] \"Cox regression analysis\" paragraph 2", "quote": "Univariate and multivariate Cox regression analyses were conducted to identify signatures independently associated with overall survival (OS)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material. 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