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pmid:36092924

Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature.

Xueliang Zhou · Batuer Aikemu · Shuchun Li · Yanfei Shao · Hongtao Jia · Ling Huang · Hiju Hong · Sen Zhang · Qiushi Tang · Ruijun Pan · Jing Sun · Minhua Zheng

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.962575

Paper

complete

Experiment

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Data

partial

Analysis

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Execution

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title
Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature.
doi
10.3389/fgene.2022.962575
pmid
36092924
authors array · 12 items
[0]
Xueliang Zhou
[1]
Batuer Aikemu
[2]
Shuchun Li
[3]
Yanfei Shao
[4]
Hongtao Jia
[5]
Ling Huang
[6]
Hiju Hong
[7]
Sen Zhang
[8]
Qiushi Tang
[9]
Ruijun Pan
[10]
Jing Sun
[11]
Minhua Zheng
journal
Frontiers in genetics
year
2022
abstract
Colorectal cancer (CRC) is one of the most common malignant tumors with a high incidence rate and mortality. LncRNA is an important regulator of the immune system. It is of great significance to study immune-related lncRNAs (IR-lncRNAs) for CRC. In this study, we screened IR-lncRNAs differentially expressed in normal and CRC tissues, and Univariate Cox regression and the Least Absolute Shrinkage and Selection Operator were applied to construct IR-lncRNA prognostic signature in TCGA training dataset, and its predictive capability for the prognosis of CRC patients was verified in GSE39582 validation dataset. The novel signature was identified as an independent predictor of prognosis in CRC patients. In addition, the signature could accurately predict the feature of the immune microenvironment and therapeutic response in CRC patients. The CMap database was adopted to screen for small molecule candidate drugs that can reverse and treat high-risk CRC patients. Finally, the expression of six IR-lncRNAs were verified by qRT-PCR in clinical specimens from our patient cohort. In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.
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The optimal lambda value was obtained by LASSO Cox regression and cross-validation.
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sections[17] "Construction of IR-lncRNA prognostic signature" paragraph 2
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The optimal lambda value was obtained by LASSO Cox regression and cross-validation.
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In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.
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In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.
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In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.
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GSM972522
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
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false
licence_read
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[0]
asset:data:geo:GSE39582 not downloaded
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asset:data:geo:GSE39582 licence not read
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partial
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method-1
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survival_analysis
specific
cox_proportional_hazards
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Survival analysis
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[0]
cox_ph
missing_operations array · 0 items
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data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
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1
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verbatim
quote
The optimal lambda value was obtained by LASSO Cox regression and cross-validation.
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id
method-2
family
group_comparison
specific
wilcoxon
label
Group comparison
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missing_operations array · 1 item
[0]
group_comparison_wilcoxon
expressible
false
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data_shapes array · 1 item
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two_or_more_groups_continuous
evidence object · 3 fields
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method-3
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survival_analysis
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Survival analysis
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[0]
survival_km
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data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
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0.8
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high
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[3] object · 10 fields
id
method-4
family
epidemiological_modelling
specific
incidence_rate
label
Epidemiological rate modelling
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[0]
incidence_rate_model
[1]
offset_regression
missing_operations array · 0 items
parameters object · 0 fields
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[0]
event_counts_with_exposure_time
evidence object · 3 fields
score
0.7
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medium
quote
incidence rate
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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]
machine_learning
[2]
survival_analysis
[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
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readiness object · 8 fields
state
complete
tier
R1
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nothing:replicable_now
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method object · 5 fields
tier
R1
expressible
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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 · 1 item
[0]
GSE39582
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[0]
GSE39582
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[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 GSE39582 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
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[0]
cox_ph
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[0]
source:pmid:36092924
[1]
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must_build object · 5 fields
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[0]
data:geo:GSE39582
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state
partial
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kind
extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:05:07Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
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14824
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2909
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256
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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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minimax
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[2]
review.human_critique
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absent
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not_run
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null
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gaps array · 1 item
[0]
execution.not_run
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entities array · 3 items
[0] object · 3 fields
id
pmid:36092924
type
paper
label
pmid:36092924
[1] object · 3 fields
id
source:pmid:36092924
type
manuscript
label
PMID 36092924 full text
[2] object · 3 fields
id
data:geo:GSE39582
type
dataset
label
GEO GSE39582
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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id
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type
paper
label
pmid:36092924
[1] object · 3 fields
id
source:pmid:36092924
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manuscript
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PMID 36092924 full text
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id
data:geo:GSE39582
type
dataset
label
GEO GSE39582
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-36092924
type
extraction
used array · 1 item
[0]
source:pmid:36092924
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE39582
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE39582
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
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agent:corpus-assay-engine
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software
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Corpus assay engine
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id
agent:minimax-reader
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MiniMax literature reader
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343fb30756ba6ec3
capability_table_fingerprint
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ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:36092924
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sha256:934c879c64153589f024f707e2ff8ea2e1860e7ed09c544ac5fbc36c3e7a0502
fork_of
null
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[4]
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supported
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f2132e96ae6c7a4e
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The optimal lambda value was obtained by LASSO Cox regression and cross-validation.
order_basis
analysis_only
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36092924", "kind": "science-record", "revision": 4, "content_hash": "sha256:fd3b5a25500db53cbf88e78a43a898fad695e052a4481846a482820e3ef2e739", "created_at": "2026-11-01T18:15:20Z", "updated_at": "2026-11-01T22:07:32Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature.", "doi": "10.3389/fgene.2022.962575", "pmid": "36092924", "authors": ["Xueliang Zhou", "Batuer Aikemu", "Shuchun Li", "Yanfei Shao", "Hongtao Jia", "Ling Huang", "Hiju Hong", "Sen Zhang", "Qiushi Tang", "Ruijun Pan", "Jing Sun", "Minhua Zheng"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "Colorectal cancer (CRC) is one of the most common malignant tumors with a high incidence rate and mortality. LncRNA is an important regulator of the immune system. It is of great significance to study immune-related lncRNAs (IR-lncRNAs) for CRC. In this study, we screened IR-lncRNAs differentially expressed in normal and CRC tissues, and Univariate Cox regression and the Least Absolute Shrinkage and Selection Operator were applied to construct IR-lncRNA prognostic signature in TCGA training dataset, and its predictive capability for the prognosis of CRC patients was verified in GSE39582 validation dataset. The novel signature was identified as an independent predictor of prognosis in CRC patients. In addition, the signature could accurately predict the feature of the immune microenvironment and therapeutic response in CRC patients. The CMap database was adopted to screen for small molecule candidate drugs that can reverse and treat high-risk CRC patients. Finally, the expression of six IR-lncRNAs were verified by qRT-PCR in clinical specimens from our patient cohort. In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.", "claims": [{"id": "claim-method", "statement": "The optimal lambda value was obtained by LASSO Cox regression and cross-validation.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36092924", "locator": "sections[17] \"Construction of IR-lncRNA prognostic signature\" paragraph 2", "quote": "The optimal lambda value was obtained by LASSO Cox regression and cross-validation."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE39582"], "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:GSE39582"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36092924", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2022.962575", "sha256": "sha256:6d3b74b1cb87398222f97f578f50ecbe54c4b9386446ae72b38f835c85d0679b", "bytes": 55774, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fgene.2022.962575", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9454821", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE39582", "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=GSE39582", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE39582", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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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": false}}], "gaps": ["asset:data:geo:GSE39582 not downloaded", "asset:data:geo:GSE39582 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "The optimal lambda value was obtained by LASSO Cox regression and cross-validation."}}, {"id": "method-2", "family": "group_comparison", "specific": "wilcoxon", "label": "Group comparison", "dsl_operations": [], "missing_operations": 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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": ["GSE39582"], "resolved_accessions": ["GSE39582"], "statements": ["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 GSE39582 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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