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pmid:37920710

Immune-related gene-based model predicts the survival of colorectal carcinoma and reflected various biological statuses.

Zhengchun Kang · Bingchen Chen · Xiuzhu Ma · Feihu Yan · Zhen Wang

Frontiers in molecular biosciences · 2023 doi:10.3389/fmolb.2023.1277933

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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pmid:37920710
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title
Immune-related gene-based model predicts the survival of colorectal carcinoma and reflected various biological statuses.
doi
10.3389/fmolb.2023.1277933
pmid
37920710
authors array · 5 items
[0]
Zhengchun Kang
[1]
Bingchen Chen
[2]
Xiuzhu Ma
[3]
Feihu Yan
[4]
Zhen Wang
journal
Frontiers in molecular biosciences
year
2023
abstract
Bakcground: Prognosis of colorectal cancer (CRC) varies due to complex genetic-microenviromental interactions, and multiple gene-based prognostic models have been highlighted. Material and Method: In this work, the immune-related genes' expression-based model was developed and the scores of each sample were calculated. The correlation between the model and clinical information, immune infiltration, drug response and biological pathways were analyzed. Results: The high-score samples have a significantly longer survival (overall survival and progression-free survival) period than those with a low score, which was validated across seven datasets containing 1,325 samples (GSE17536 (N = 115), GSE17537 (N = 55), GSE33113 (N = 90), GSE37892 (N = 130), GSE38832 (N = 74), GSE39582 (N = 481), and TCGA (N = 380)). The score is significantly associated with clinical indicators, including age and stage, and further associated with PD-1/PD-L1 gene expression. Furthermore, high-score samples have significantly higher APC and a lower MUC5B mutation rate. The high-score samples show more immune infiltration (including CD4+ and CD8+ T cells, M1/M2 macrophages, and NK cells). Enriched pathway analyses showed that cancer-related pathways, including immune-related pathways, were significantly activated in high-score samples and that some drugs have significantly lower IC50 values than those with low score. Conclusion: The model developed based on immune-related genes is robust and reflected various statuses of CRC and may be a potential clinical indicator.
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Differentially mutated genes between groups were evaluated using Fisher’s exact test (only non-synonymous mutation used), and significantly different (p <0.05) mutations were identified.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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High-score samples have a significantly higher APC mutation rate and a lower MUC5B mutation rate than low-score samples (p <0.05).
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By comparing high-/low-score samples, it is found that the APC gene mutation rate of high-score samples is significantly higher than that of low-score samples, while MUC5B values are lower in high-score samples (p <0.05; Figure 4A).
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sections[6] "Genetic signature of high-score samples" paragraph 2
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By comparing high-/low-score samples, it is found that the APC gene mutation rate of high-score samples is significantly higher than that of low-score samples, while MUC5B values are lower in high-score samples (p <0.05; Figure 4A).
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Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients (Moffitt Samples)
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Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients (VMC Samples)
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[56]
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[57]
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[58]
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[59]
GSM929553
[60]
GSM929554
[61]
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[62]
GSM929556
[63]
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[64]
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[65]
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[66]
GSM929560
[67]
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[68]
GSM929562
[69]
GSM929563
[70]
GSM929564
[71]
GSM929565
[72]
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[73]
GSM929567
[74]
GSM929568
[75]
GSM929569
[76]
GSM929570
[77]
GSM929571
[78]
GSM929572
[79]
GSM929573
[80]
GSM929574
[81]
GSM929575
[82]
GSM929576
[83]
GSM929577
[84]
GSM929578
[85]
GSM929579
[86]
GSM929580
[87]
GSM929581
[88]
GSM929582
[89]
GSM929583
[90]
GSM929584
[91]
GSM929585
[92]
GSM929586
[93]
GSM929587
[94]
GSM929588
[95]
GSM929589
[96]
GSM929590
[97]
GSM929591
[98]
GSM929592
[99]
GSM929593
[100]
GSM929594
[101]
GSM929595
[102]
GSM929596
[103]
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[104]
GSM929598
[105]
GSM929599
[106]
GSM929600
[107]
GSM929601
[108]
GSM929602
[109]
GSM929603
[110]
GSM929604
[111]
GSM929605
[112]
GSM929606
[113]
GSM929607
[114]
GSM929608
[115]
GSM929609
[116]
GSM929610
[117]
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[118]
GSM929612
[119]
GSM929613
[120]
GSM929614
[121]
GSM929615
[122]
GSM929616
[123]
GSM929617
[124]
GSM929618
[125]
GSM929619
[126]
GSM929620
[127]
GSM929621
[128]
GSM929622
[129]
GSM929623
sample_count
130
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
A seven-gene signature aggregates a subgroup of stage II colon cancers with stage III.
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[5] object · 15 fields
id
data:geo:GSE38832
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=GSE38832
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE38832
version
null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
access_statement_kind
data_availability_statement
sample_accessions array · 122 items
[0]
GSM950411
[1]
GSM950412
[2]
GSM950413
[3]
GSM950414
[4]
GSM950415
[5]
GSM950416
[6]
GSM950417
[7]
GSM950418
[8]
GSM950419
[9]
GSM950420
[10]
GSM950421
[11]
GSM950422
[12]
GSM950423
[13]
GSM950424
[14]
GSM950425
[15]
GSM950426
[16]
GSM950427
[17]
GSM950428
[18]
GSM950429
[19]
GSM950430
[20]
GSM950431
[21]
GSM950432
[22]
GSM950433
[23]
GSM950434
[24]
GSM950435
[25]
GSM950436
[26]
GSM950437
[27]
GSM950438
[28]
GSM950439
[29]
GSM950440
[30]
GSM950441
[31]
GSM950442
[32]
GSM950443
[33]
GSM950444
[34]
GSM950445
[35]
GSM950446
[36]
GSM950447
[37]
GSM950448
[38]
GSM950449
[39]
GSM950450
[40]
GSM950451
[41]
GSM950452
[42]
GSM950453
[43]
GSM950454
[44]
GSM950455
[45]
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[46]
GSM950457
[47]
GSM950458
[48]
GSM950459
[49]
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[50]
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[51]
GSM950462
[52]
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[53]
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[54]
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[55]
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[56]
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[57]
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[58]
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[59]
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[60]
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[61]
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[62]
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[63]
GSM950474
[64]
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[65]
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[66]
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[67]
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[68]
GSM950479
[69]
GSM950480
[70]
GSM950481
[71]
GSM950482
[72]
GSM950483
[73]
GSM950484
[74]
GSM950485
[75]
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[76]
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[77]
GSM950488
[78]
GSM950489
[79]
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[80]
GSM950491
[81]
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[82]
GSM950493
[83]
GSM950494
[84]
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[85]
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[86]
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[87]
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[88]
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[89]
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[90]
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[91]
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[92]
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[93]
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[94]
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[95]
GSM950506
[96]
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[97]
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[98]
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[99]
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[100]
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[101]
GSM950512
[102]
GSM950513
[103]
GSM950514
[104]
GSM950515
[105]
GSM950516
[106]
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[107]
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[108]
GSM950519
[109]
GSM950520
[110]
GSM950521
[111]
GSM950522
[112]
GSM950523
[113]
GSM950524
[114]
GSM950525
[115]
GSM950526
[116]
GSM950527
[117]
GSM950528
[118]
GSM950529
[119]
GSM950530
[120]
GSM950531
[121]
GSM950532
sample_count
122
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
NFAT transcriptional activity is associated with metastatic capacity in colon cancer
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 10 items
[0]
asset:data:geo:GSE17536 not downloaded
[1]
asset:data:geo:GSE17536 licence not read
[2]
asset:data:geo:GSE17537 not downloaded
[3]
asset:data:geo:GSE17537 licence not read
[4]
asset:data:geo:GSE33113 not downloaded
[5]
asset:data:geo:GSE33113 licence not read
[6]
asset:data:geo:GSE37892 not downloaded
[7]
asset:data:geo:GSE37892 licence not read
[8]
asset:data:geo:GSE38832 not downloaded
[9]
asset:data:geo:GSE38832 licence not read
analysis object · 4 fields
state
partial
methods array · 1 item
[0] object · 10 fields
id
method-1
family
null
specific
null
label
Fisher’s exact test
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Differentially mutated genes between groups were evaluated using Fisher’s exact test (only non-synonymous mutation used), and significantly different (p <0.05) mutations were identified.
targets array · 1 item
[0] object · 8 fields
id
target-published-estimate
claim_id
claim-target-result
operation
null
unit
p-value
tolerance
null
state
complete
note
The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold.
gaps array · 1 item
[0]
method.reader_named_unmapped
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
blocked
tier
R4
blocking_axis
method
blocked_on
method:not_determinable
axes object · 3 fields
method object · 5 fields
tier
R4
expressible
false
required_operations array · 0 items
missing_operations array · 0 items
basis
The reader quoted the method the paper names (Fisher’s exact test), but the corpus's method extractor could not map it onto a DSL operation, so the method is published but not expressible.
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 · 5 items
[0]
GSE17536
[1]
GSE17537
[2]
GSE33113
[3]
GSE38832
[4]
GSE37892
resolved_accessions array · 5 items
[0]
GSE17536
[1]
GSE17537
[2]
GSE33113
[3]
GSE38832
[4]
GSE37892
statements array · 1 item
[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
basis
The paper names GSE17536, GSE17537, GSE33113, GSE38832, GSE37892 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 · 0 items
assets array · 2 items
[0]
source:pmid:37920710
[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 · 1 item
[0]
method:not_determinable
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
2026-11-01T18:58:06Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
13079
completion_tokens
1976
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:37920710
type
paper
label
pmid:37920710
[1] object · 3 fields
id
source:pmid:37920710
type
manuscript
label
PMID 37920710 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:37920710
type
paper
label
pmid:37920710
[1] object · 3 fields
id
source:pmid:37920710
type
manuscript
label
PMID 37920710 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-37920710
type
extraction
used array · 1 item
[0]
source:pmid:37920710
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
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:37920710
parent_hash
sha256:fea9d0029fc074de41b8fadf1805ecbbeca652e79c1e766d10b222d357409e5e
fork_of
null
gaps array · 15 items
[0]
asset:data:geo:GSE17536 licence not read
[1]
asset:data:geo:GSE17536 not downloaded
[2]
asset:data:geo:GSE17537 licence not read
[3]
asset:data:geo:GSE17537 not downloaded
[4]
asset:data:geo:GSE33113 licence not read
[5]
asset:data:geo:GSE33113 not downloaded
[6]
asset:data:geo:GSE37892 licence not read
[7]
asset:data:geo:GSE37892 not downloaded
[8]
asset:data:geo:GSE38832 licence not read
[9]
asset:data:geo:GSE38832 not downloaded
[10]
execution.not_run
[11]
method.reader_named_unmapped
[12]
review.human_critique
[13]
review.independent_reader
[14]
review.machine_critique
Complete file
{"sci_version": "1.0", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37920710", "kind": "science-record", "revision": 2, "content_hash": "sha256:baa825447a670b873fe1b00e55ad3458d1ae6a0debda5dcb87da51c84a2a9dff", "created_at": "2026-11-01T19:02:48Z", "updated_at": "2026-11-01T21:31:51Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Immune-related gene-based model predicts the survival of colorectal carcinoma and reflected various biological statuses.", "doi": "10.3389/fmolb.2023.1277933", "pmid": "37920710", "authors": ["Zhengchun Kang", "Bingchen Chen", "Xiuzhu Ma", "Feihu Yan", "Zhen Wang"], "journal": "Frontiers in molecular biosciences", "year": 2023, "abstract": "Bakcground: Prognosis of colorectal cancer (CRC) varies due to complex genetic-microenviromental interactions, and multiple gene-based prognostic models have been highlighted. Material and Method: In this work, the immune-related genes' expression-based model was developed and the scores of each sample were calculated. The correlation between the model and clinical information, immune infiltration, drug response and biological pathways were analyzed. Results: The high-score samples have a significantly longer survival (overall survival and progression-free survival) period than those with a low score, which was validated across seven datasets containing 1,325 samples (GSE17536 (N = 115), GSE17537 (N = 55), GSE33113 (N = 90), GSE37892 (N = 130), GSE38832 (N = 74), GSE39582 (N = 481), and TCGA (N = 380)). The score is significantly associated with clinical indicators, including age and stage, and further associated with PD-1/PD-L1 gene expression. Furthermore, high-score samples have significantly higher APC and a lower MUC5B mutation rate. The high-score samples show more immune infiltration (including CD4+ and CD8+ T cells, M1/M2 macrophages, and NK cells). Enriched pathway analyses showed that cancer-related pathways, including immune-related pathways, were significantly activated in high-score samples and that some drugs have significantly lower IC50 values than those with low score. Conclusion: The model developed based on immune-related genes is robust and reflected various statuses of CRC and may be a potential clinical indicator.", "claims": [{"id": "claim-method", "statement": "Differentially mutated genes between groups were evaluated using Fisher’s exact test (only non-synonymous mutation used), and significantly different (p <0.05) mutations were identified.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37920710", "locator": "sections[16] \"Genetic association\" paragraph 2", "quote": "Differentially mutated genes between groups were evaluated using Fisher’s exact test (only non-synonymous mutation used), and significantly different (p <0.05) mutations were identified."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37920710", "locator": "sections[23] \"Data availability statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "High-score samples have a significantly higher APC mutation rate and a lower MUC5B mutation rate than low-score samples (p <0.05).", "kind": "quantitative", "target": {"value": 0.05, "unit": "p-value", "tolerance": null, "source": "By comparing high-/low-score samples, it is found that the APC gene mutation rate of high-score samples is significantly higher than that of low-score samples, while MUC5B values are lower in high-score samples (p <0.05; Figure 4A)."}, "evidence": [{"asset": "source:pmid:37920710", "locator": "sections[6] \"Genetic signature of high-score samples\" paragraph 2", "quote": "By comparing high-/low-score samples, it is found that the APC gene mutation rate of high-score samples is significantly higher than that of low-score samples, while MUC5B values are lower in high-score samples (p <0.05; Figure 4A)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "High-score samples have a significantly higher APC mutation rate and a lower MUC5B mutation rate than low-score samples (p <0.05).", "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:37920710"], "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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