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pmid:36147506

A novel immune-related radioresistant lncRNAs signature based model for risk stratification and prognosis prediction in esophageal squamous cell carcinoma.

Jianqing Zheng · Xiaohui Chen · Bifen Huang · Jiancheng Li

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.921902

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Experiment

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Data

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Analysis

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title
A novel immune-related radioresistant lncRNAs signature based model for risk stratification and prognosis prediction in esophageal squamous cell carcinoma.
doi
10.3389/fgene.2022.921902
pmid
36147506
authors array · 4 items
[0]
Jianqing Zheng
[1]
Xiaohui Chen
[2]
Bifen Huang
[3]
Jiancheng Li
journal
Frontiers in genetics
year
2022
abstract
Background and purpose: Radioresistance remains a major reason of radiotherapeutic failure in esophageal squamous cell carcinoma (ESCC). Our study is to screen the immune-related long non-coding RNA (ir-lncRNAs) of radiation-resistant ESCC (rr-ESCC) via Gene Expression Omnibus (GEO) database and to construct a prognostic risk model. Methods: Microarray data (GSE45670) related to radioresistance of ESCC was downloaded from GEO. Based on pathologic responses after chemoradiotherapy, patients were divided into a non-responder (17 samples) and responder group (11 samples), and the difference in expression profiles of ir-lncRNAs were compared therein. Ir-lncRNA pairs were constructed for the differentially expressed lncRNAs as prognostic variables, and the microarray dataset (GSE53625) was downloaded from GEO to verify the effect of ir-lncRNA pairs on the long-term survival of ESCC. After modelling, patients are divided into high- and low-risk groups according to prognostic risk scores, and the outcomes were compared within groups based on the COX proportional hazards model. The different expression of ir-lncRNAs were validated using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened in the GSE45670 dataset with differential expression, and 180 ir-lncRNA pairs were constructed. After matching with ir-lncRNA pairs constructed by GSE53625, six ir-lncRNA pairs had a significant impact on the prognosis of ESCC from univariate analysis model, of which three ir-lncRNA pairs were significantly associated with prognosis in multivariate COX analysis. These three lncRNA pairs were used as prognostic indicators to construct a prognostic risk model, and the predicted risk scores were calculated. With a median value of 2.371, the patients were divided into two groups. The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001). The 1-, 2-, and 3-year prediction performance of this risk-model was 0.666, 0.702, and 0.686, respectively. In the validation setting, three ir-lncRNAs were significantly up-regulated, while two ir-lncRNAs were obviouly down-regulated in the responder group. Conclusion: Ir-lncRNAs may be involved in the biological regulation of radioresistance in patients with ESCC; and the prognostic risk-model, established by three ir-lncRNAs pairs has important clinical value in predicting the prognosis of patients with rr-ESCC.
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Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs.
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sections[5] "Construction of the predictive model" paragraph 3
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Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs.
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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 author.
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A prognostic risk model based on three immune-related lncRNA pairs separated ESCC patients into high- and low-risk groups with significantly different overall survival (p < 0.001).
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The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001).
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These three lncRNA pairs were used as prognostic indicators to construct a prognostic risk model, and the predicted risk scores were calculated.
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The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001).
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A prognostic risk model based on three immune-related lncRNA pairs separated ESCC patients into high- and low-risk groups with significantly different overall survival (p < 0.001).
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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[0]
cox_ph
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[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
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verbatim
quote
Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs.
[1] object · 10 fields
id
method-2
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group_comparison
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wilcoxon
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[0]
group_comparison_wilcoxon
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false
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two_or_more_groups_continuous
evidence object · 3 fields
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0.8
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high
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Wilcoxon
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method-3
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group_comparison
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anova
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Group comparison
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[0]
group_summary
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[2]
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[3]
group_comparison_anova
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two_or_more_groups_continuous
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0.8
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high
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id
method-4
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survival_analysis
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kaplan_meier
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Survival analysis
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[0]
survival_km
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[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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Kaplan-Meier
[4] object · 10 fields
id
method-5
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network_analysis
specific
pathway_enrichment
label
Network / pathway analysis
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[0]
pathway_enrich
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[0]
edge_list
evidence object · 3 fields
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0.8
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high
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pathway enrichment
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target-published-estimate
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claim-target-result
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p-value
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null
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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.
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[0]
method.reader_differs_from_extractor
capability object · 3 fields
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complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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meta_analysis
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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complete
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nothing:replicable_now
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true
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cox_ph
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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
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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.
data object · 6 fields
tier
R1
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true
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[0]
GSE45670
[1]
GSE53625
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[0]
GSE45670
[1]
GSE53625
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 author.
basis
The paper names GSE45670, GSE53625 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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cox_ph
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[0]
source:pmid:36147506
[1]
data:geo:GSE45670
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data:geo:GSE45670
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:06:39Z
independence
single_reader
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verbatim
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verbatim
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5
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13448
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256
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extraction
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pmid:36147506
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paper
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pmid:36147506
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source:pmid:36147506
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manuscript
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PMID 36147506 full text
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data:geo:GSE45670
type
dataset
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GEO GSE45670
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
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pmid:36147506
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paper
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pmid:36147506
[1] object · 3 fields
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source:pmid:36147506
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manuscript
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PMID 36147506 full text
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data:geo:GSE45670
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dataset
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GEO GSE45670
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agent:corpus-assay-engine
[1] object · 4 fields
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activity-read-36147506
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extraction
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agent:minimax-reader
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activity-resolve-GSE45670
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agent:corpus-assay-engine
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pmid:36147506
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sha256:4f33557b5cd9ca7ce90d766fff1ca6a2c4bddebb621eac1ef0c1c4794950e734
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asset:data:geo:GSE45670 licence not read
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asset:data:geo:GSE45670 not downloaded
[2]
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[3]
asset:data:geo:GSE53625 not downloaded
[4]
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[5]
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[6]
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[0] object · 11 fields
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data_generation
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99e1195c7d6f
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99e1195c7d6f
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[0]
construct a prognostic risk model. Methods: Microarray data (GSE45670) related to radioresistance o
[1]
sed lncRNAs as prognostic variables, and the microarray dataset (GSE53625) was downloaded from GEO t
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paper_text_order:456
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99e1195c7d6f
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[0]
ed using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened i
[1]
using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened i
[2]
expression levels of ir-lncRNAs detected by RT-qPCR, *p < 0.05, **p < 0.01, ***p < 0.001. Click
[3]
pression levels of ir-lncRNAs detected by RT-qPCR, *p < 0.05, **p < 0.01, ***p < 0.001. Click
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cox_ph
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f2132e96ae6c7a4e
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Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36147506", "kind": "science-record", "revision": 4, "content_hash": "sha256:56f660218f27ab06410f241efc0a1c8020420f9c04be876a7d7aa119bbe8cee1", "created_at": "2026-11-01T18:15:26Z", "updated_at": "2026-11-01T22:07:38Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A novel immune-related radioresistant lncRNAs signature based model for risk stratification and prognosis prediction in esophageal squamous cell carcinoma.", "doi": "10.3389/fgene.2022.921902", "pmid": "36147506", "authors": ["Jianqing Zheng", "Xiaohui Chen", "Bifen Huang", "Jiancheng Li"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "Background and purpose: Radioresistance remains a major reason of radiotherapeutic failure in esophageal squamous cell carcinoma (ESCC). Our study is to screen the immune-related long non-coding RNA (ir-lncRNAs) of radiation-resistant ESCC (rr-ESCC) via Gene Expression Omnibus (GEO) database and to construct a prognostic risk model. Methods: Microarray data (GSE45670) related to radioresistance of ESCC was downloaded from GEO. Based on pathologic responses after chemoradiotherapy, patients were divided into a non-responder (17 samples) and responder group (11 samples), and the difference in expression profiles of ir-lncRNAs were compared therein. Ir-lncRNA pairs were constructed for the differentially expressed lncRNAs as prognostic variables, and the microarray dataset (GSE53625) was downloaded from GEO to verify the effect of ir-lncRNA pairs on the long-term survival of ESCC. After modelling, patients are divided into high- and low-risk groups according to prognostic risk scores, and the outcomes were compared within groups based on the COX proportional hazards model. The different expression of ir-lncRNAs were validated using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened in the GSE45670 dataset with differential expression, and 180 ir-lncRNA pairs were constructed. After matching with ir-lncRNA pairs constructed by GSE53625, six ir-lncRNA pairs had a significant impact on the prognosis of ESCC from univariate analysis model, of which three ir-lncRNA pairs were significantly associated with prognosis in multivariate COX analysis. These three lncRNA pairs were used as prognostic indicators to construct a prognostic risk model, and the predicted risk scores were calculated. With a median value of 2.371, the patients were divided into two groups. The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001). The 1-, 2-, and 3-year prediction performance of this risk-model was 0.666, 0.702, and 0.686, respectively. In the validation setting, three ir-lncRNAs were significantly up-regulated, while two ir-lncRNAs were obviouly down-regulated in the responder group. Conclusion: Ir-lncRNAs may be involved in the biological regulation of radioresistance in patients with ESCC; and the prognostic risk-model, established by three ir-lncRNAs pairs has important clinical value in predicting the prognosis of patients with rr-ESCC.", "claims": [{"id": "claim-method", "statement": "Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36147506", "locator": "sections[5] \"Construction of the predictive model\" paragraph 3", "quote": "Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36147506", "locator": "sections[23] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A prognostic risk model based on three immune-related lncRNA pairs separated ESCC patients into high- and low-risk groups with significantly different overall survival (p < 0.001).", "kind": "quantitative", "target": {"value": 0.001, "unit": "p-value", "tolerance": null, "source": "The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001)."}, "evidence": [{"asset": "source:pmid:36147506", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "These three lncRNA pairs were used as prognostic indicators to construct a prognostic risk model, and the predicted risk scores were calculated."}, {"asset": "source:pmid:36147506", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The overall survival (OS) in the high-risk group was significantly worse than that in the low-risk group (p < 0.001)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A prognostic risk model based on three immune-related lncRNA pairs separated ESCC patients into high- and low-risk groups with significantly different overall survival (p < 0.001).", "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:36147506"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE45670"], "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:GSE45670"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36147506", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2022.921902", "sha256": 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null, "platform": "570", "taxon": "Homo sapiens", "title": "Expression data from esophageal squamous cell carcinomas and normal esophageal epithelia", "resolution_checked_at": "2026-11-01T15:39:54Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE53625", "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=GSE53625", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE53625", "version": null, "note": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The original contributions presented in 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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": ["GSE45670", "GSE53625"], "resolved_accessions": ["GSE45670", "GSE53625"], "statements": ["The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author."], "basis": "The paper names GSE45670, GSE53625 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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Methods: Microarray data (GSE45670) related to radioresistance o", "sed lncRNAs as prognostic variables, and the microarray dataset (GSE53625) was downloaded from GEO t"], "order_basis": "paper_text_order:456", "id": "assay:1"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["ed using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened i", "using ECA 109 and ECA 109R cell lines via RT-qPCR. Results: 26 ir-lncRNA genes were screened i", "expression levels of ir-lncRNAs detected by RT-qPCR, *p < 0.05, **p < 0.01, ***p < 0.001. Click", "pression levels of ir-lncRNAs detected by RT-qPCR, *p < 0.05, **p < 0.01, ***p < 0.001. Click"], "order_basis": "paper_text_order:1294", "id": "assay:2"}, {"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Univariate and multivariate Cox regression survival analyses were performed using the “survival” package in R 4.1.2 software to screen ir-lncRNAs with significant impact on prognosis. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to narrow down the prognostically significant ir-lncRNA pairs."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}