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pmid:39386801

CD8+ T cell associated scoring model helps prognostic diagnosis and immunotherapy selection in patients with colon adenocarcinoma.

Zheng Zhao · Mingkai Chen · Kuanxue Sun · Xinqi Gu

Heliyon · 2024 doi:10.1016/j.heliyon.2024.e37998

Paper

complete

Experiment

complete

Data

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Analysis

partial

Execution

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title
CD8+ T cell associated scoring model helps prognostic diagnosis and immunotherapy selection in patients with colon adenocarcinoma.
doi
10.1016/j.heliyon.2024.e37998
pmid
39386801
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[0]
Zheng Zhao
[1]
Mingkai Chen
[2]
Kuanxue Sun
[3]
Xinqi Gu
journal
Heliyon
year
2024
abstract
Objective: T cell-mediated immunity plays a crucial role in the immune response against tumors, with CD 8+ T cells playing a leading role in the eradication of cancer cells. Material and methods: A total of 5 datasets were included in this study. Single cell transcriptome data were used to discover CD8+ T cell marker genes, and Bulk transcriptome data from TCGA and GEO were jointly analyzed to screen candidate prognostic genes. lasso regression was performed to construct prognostic models. Immunotherapy cohort (IMvigor 210 and GSE78220) was applied to validate the diagnostic power of markers. Result: Single-cell transcriptome data identified 65 CD8+ T cell marker genes, highlighting their importance in T cell-mediated immune responses. Among these, 11 genes were identified as CD8+ T-associated differential genes through analysis of bulk data from TCGA and GEO. A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups. This model exhibited higher prognostic accuracy compared to traditional clinicopathological characteristics (age, pathological stage, histological grading). Moreover, the risk score derived from this model successfully differentiated patient responses to immunotherapy, as validated in the IMvigor 210 and GSE78220 cohorts. Conclusion: Our research introduces a novel prognostic signature based on CD8+ T cell marker genes, demonstrating significant predictive power for prognosis and immunotherapy response in COAD patients. This model offers a potential tool for improving patient stratification and personalizing treatment strategies.
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Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model.
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sections[11] "Establishment and validation of a 5-gene prognostic signature based on CD8+ T cell marker genes" paragraph 2
quote
Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model.
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All data sets used in this study are public data sets. The datasets generated analyzed during the current study are available in the GEO and TCGA repository, including GSE146771, GSE39582, GSE78220, TCGA-COAD and IMvigor210. The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request.
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sections[20] "Data availability statement" paragraph 2
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All data sets used in this study are public data sets. The datasets generated analyzed during the current study are available in the GEO and TCGA repository, including GSE146771, GSE39582, GSE78220, TCGA-COAD and IMvigor210. The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request.
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A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups.
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A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups.
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A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups.
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sample_count
585
group_sizes
null
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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
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licence_read
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[3] object · 15 fields
id
data:geo:GSE78220
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geo-series
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE78220
sha256
null
bytes
null
access
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resolved
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null
reader_status
reader_required
identifier
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version
null
note
All data sets used in this study are public data sets. The datasets generated analyzed during the current study are available in the GEO and TCGA repository, including GSE146771, GSE39582, GSE78220, TCGA-COAD and IMvigor210. The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
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All data sets used in this study are public data sets. The datasets generated analyzed during the current study are available in the GEO and TCGA repository, including GSE146771, GSE39582, GSE78220, TCGA-COAD and IMvigor210. The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 28 items
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[27]
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sample_count
28
group_sizes
null
group_sizes_basis
null
platform
11154
taxon
Homo sapiens
title
mRNA expressions in pre-treatment melanomas undergoing anti-PD-1 checkpoint inhibition therapy
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
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[3]
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[4]
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[5]
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analysis object · 4 fields
state
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[0] object · 10 fields
id
method-1
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survival_analysis
specific
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label
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[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
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quote
Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model.
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id
method-2
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wilcoxon
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Group comparison
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missing_operations array · 1 item
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group_comparison_wilcoxon
expressible
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parameters object · 0 fields
data_shapes array · 1 item
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two_or_more_groups_continuous
evidence object · 3 fields
score
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band
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quote
Wilcoxon
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id
method-3
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survival_analysis
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kaplan_meier
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Survival analysis
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survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
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time_to_event_with_censoring
evidence object · 3 fields
score
0.8
band
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Kaplan-Meier
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method-4
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differential_expression
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limma_voom
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Differential expression analysis
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parameters object · 0 fields
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count_matrix_with_condition
evidence object · 3 fields
score
0.8
band
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quote
limma
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id
method-5
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diagnostic_evaluation
specific
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Diagnostic test evaluation
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parameters object · 0 fields
data_shapes array · 1 item
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reference_standard_and_test
evidence object · 3 fields
score
0.8
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high
quote
ROC curve
[5] object · 10 fields
id
method-6
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
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[0]
chi_square_test
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parameters object · 0 fields
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evidence object · 3 fields
score
0.8
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chi-square
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gaps array · 1 item
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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
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meta_analysis
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
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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]
GSE146771
[1]
GSE39582
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GSE78220
resolved_accessions array · 3 items
[0]
GSE146771
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GSE39582
[2]
GSE78220
statements array · 1 item
[0]
All data sets used in this study are public data sets. The datasets generated analyzed during the current study are available in the GEO and TCGA repository, including GSE146771, GSE39582, GSE78220, TCGA-COAD and IMvigor210. The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request.
basis
The paper names GSE146771, GSE39582, GSE78220 in TISCH2 and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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cox_ph
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[0]
source:pmid:39386801
[1]
data:geo:GSE146771
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run_analysis
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE146771
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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
2026-11-01T19:34:33Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
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5
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11944
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128
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
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entities array · 3 items
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type
paper
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source:pmid:39386801
type
manuscript
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PMID 39386801 full text
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data:geo:GSE146771
type
dataset
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GEO GSE146771
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id
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type
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paper
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pmid:39386801
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id
source:pmid:39386801
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type
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agent:corpus-assay-engine
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extraction
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agent:minimax-reader
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activity-resolve-GSE146771
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agent:corpus-assay-engine
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f2132e96ae6c7a4e
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Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39386801", "kind": "science-record", "revision": 3, "content_hash": "sha256:1673069fef94d0a0e1cdc848be5da884b1cc9bd1e623f5648e21ac8b0d446b5b", "created_at": "2026-11-01T20:29:36Z", "updated_at": "2026-11-01T22:12:53Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "CD8+ T cell associated scoring model helps prognostic diagnosis and immunotherapy selection in patients with colon adenocarcinoma.", "doi": "10.1016/j.heliyon.2024.e37998", "pmid": "39386801", "authors": ["Zheng Zhao", "Mingkai Chen", "Kuanxue Sun", "Xinqi Gu"], "journal": "Heliyon", "year": 2024, "abstract": "Objective: T cell-mediated immunity plays a crucial role in the immune response against tumors, with CD 8+ T cells playing a leading role in the eradication of cancer cells.\nMaterial and methods: A total of 5 datasets were included in this study. Single cell transcriptome data were used to discover CD8+ T cell marker genes, and Bulk transcriptome data from TCGA and GEO were jointly analyzed to screen candidate prognostic genes. lasso regression was performed to construct prognostic models. Immunotherapy cohort (IMvigor 210 and GSE78220) was applied to validate the diagnostic power of markers.\nResult: Single-cell transcriptome data identified 65 CD8+ T cell marker genes, highlighting their importance in T cell-mediated immune responses. Among these, 11 genes were identified as CD8+ T-associated differential genes through analysis of bulk data from TCGA and GEO. A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups. This model exhibited higher prognostic accuracy compared to traditional clinicopathological characteristics (age, pathological stage, histological grading). Moreover, the risk score derived from this model successfully differentiated patient responses to immunotherapy, as validated in the IMvigor 210 and GSE78220 cohorts.\nConclusion: Our research introduces a novel prognostic signature based on CD8+ T cell marker genes, demonstrating significant predictive power for prognosis and immunotherapy response in COAD patients. This model offers a potential tool for improving patient stratification and personalizing treatment strategies.", "claims": [{"id": "claim-method", "statement": "Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39386801", "locator": "sections[11] \"Establishment and validation of a 5-gene prognostic signature based on CD8+ T cell marker genes\" paragraph 2", "quote": "Next, 10-fold cross-validated LASSO Cox regression analysis (Fig. 2B–C) was performed on the 11 candidate genes, and 5 genes (CXCL8, TIMP1, CPA3, SPP1, GLA) were screened for inclusion in the model."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data sets used in this study are public data sets. 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The raw data and code supporting this article can be obtained by contacting the corresponding author with a reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39386801", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A prognostic model for 5 genes was identified based on Lasso regression, dividing colon adenocarcinoma (COAD) patients into high- and low-risk groups.", "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:39386801"], "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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