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pmid:36531020

Pyroptosis-related lncRNAs: A novel prognosis signature of colorectal cancer.

Xing Cai · Xiaoqing Liang · Kun Wang · Yin Liu · Mengdi Hao · Huimin Li · Xiaofang Dai · Lei Ding

Frontiers in oncology · 2022 doi:10.3389/fonc.2022.983895

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Experiment

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Data

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title
Pyroptosis-related lncRNAs: A novel prognosis signature of colorectal cancer.
doi
10.3389/fonc.2022.983895
pmid
36531020
authors array · 8 items
[0]
Xing Cai
[1]
Xiaoqing Liang
[2]
Kun Wang
[3]
Yin Liu
[4]
Mengdi Hao
[5]
Huimin Li
[6]
Xiaofang Dai
[7]
Lei Ding
journal
Frontiers in oncology
year
2022
abstract
Pyroptosis is a newly discovered programmed cell death mechanism involved in tumorigenesis. Long non-coding RNAs (lncRNAs) have been implicated in colorectal cancer (CRC). However, the potential role of pyroptosis-related lncRNAs (PRLs) in CRC remains unelucidated. Therefore, we retrieved transcriptomic data of CRC patients from The Cancer Genome Atlas (TCGA). With the use of univariate and multivariate Cox proportional hazards regression models and the random forest algorithm, a new risk model was constructed based on eight PRLs: Z99289.2, FENDRR, CCDC144NL-ASL, TEX41, MNX1-AS1, NKILA, LINC02798, and LINC02381. Then, according to the Kaplan-Meier plots, the relationship of PRLs with the survival of CRC patients was explored and validated with our risk model in external datasets (Gene Expression Omnibus (GEO) databases; GEO17536, n = 177, and GSE161158, n = 250). To improve its clinical utility, a nomogram combining PRLs that could predict the clinical outcome of CRC patients was established. A full-spectrum immune landscape of CRC patients mediated by PRLs could be described. The PRLs were stratified into two molecular subtypes involved in immune modulators, immune infiltration of tumor immune microenvironment, and inflammatory pathways. Afterward, Tumor Immune Dysfunction and Exclusion (TIDE) and microsatellite instability (MSI) scores were analyzed. Three independent methods were applied to predict PRL-related sensitivity to chemotherapeutic drugs. Our comprehensive analysis of PRLs in CRC patients demonstrates a potential role of PRLs in predicting response to treatment and prognosis of CRC patients, which may provide a better understanding of molecular mechanisms underlying CRC pathogenesis and facilitate the development of effective immunotherapy.
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Then, a univariate Cox proportional risk regression model was used to select candidate survival-related PRLs, and p< 0.01 was set as the threshold ( Supplementary Table S4 ). Then, the random survival forests-variable hunting (RSFVH) algorithm was used to further filter the genes.
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sections[4] "The construction and validation of pyroptosis-related lncRNA prognostic model" paragraph 2
quote
Then, a univariate Cox proportional risk regression model was used to select candidate survival-related PRLs, and p< 0.01 was set as the threshold ( Supplementary Table S4 ). Then, the random survival forests-variable hunting (RSFVH) algorithm was used to further filter the genes.
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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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sections[18] "Data availability statement" paragraph 2
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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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The eight-PRL model predicted overall survival in the TCGA cohort with AUCs of 0.660, 0.768, and 0.734 at 1, 2, and 5 years, respectively, and its prognostic performance was supported in two external GEO cohorts.
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sections[11] "Survival prediction performance of the model" paragraph 2
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According to the ROC curves, PRLs might predict OS in TCGA cohort, with an AUC at 1, 2, and 5 years of 0.660, 0.768, and 0.734, respectively ( Figure 5C ).
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sections[11] "Survival prediction performance of the model" paragraph 2
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Patients in the validation cohorts with a higher risk score had a lower survival rate compared to those with a low-risk score ( Figures 5D–I ).
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The eight-PRL model predicted overall survival in the TCGA cohort with AUCs of 0.660, 0.768, and 0.734 at 1, 2, and 5 years, respectively, and its prognostic performance was supported in two external GEO cohorts.
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false
licence_read
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gaps array · 4 items
[0]
asset:data:geo:GSE161158 not downloaded
[1]
asset:data:geo:GSE161158 licence not read
[2]
asset:data:geo:GSE17536 not downloaded
[3]
asset:data:geo:GSE17536 licence not read
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state
complete
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[0] object · 10 fields
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method-1
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survival_analysis
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cox_proportional_hazards
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cox_ph
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time_to_event_with_censoring
evidence object · 3 fields
score
1
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verbatim
quote
Then, a univariate Cox proportional risk regression model was used to select candidate survival-related PRLs, and p< 0.01 was set as the threshold ( Supplementary Table S4 ). Then, the random survival forests-variable hunting (RSFVH) algorithm was used to further filter the genes.
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survival_analysis
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kaplan_meier
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Survival analysis
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time_to_event_with_censoring
evidence object · 3 fields
score
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Kaplan-Meier
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id
method-3
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machine_learning
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random_forest
label
Machine learning
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missing_operations array · 1 item
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evidence object · 3 fields
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0.7
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random forest
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state
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capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
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[5]
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
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required_operations array · 1 item
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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
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reachable
true
accessions array · 2 items
[0]
GSE17536
[1]
GSE161158
resolved_accessions array · 2 items
[0]
GSE17536
[1]
GSE161158
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 GSE17536, GSE161158 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 · 1 item
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cox_ph
assets array · 2 items
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source:pmid:36531020
[1]
data:geo:GSE161158
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run_analysis
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data:geo:GSE161158
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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
2026-11-01T18:19:59Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
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usage object · 3 fields
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15539
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[0] object · 4 fields
id
extraction
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MiniMax-M3.1-Flash
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minimax
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null
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gaps array · 1 item
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provenance object · 7 fields
entities array · 3 items
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id
pmid:36531020
type
paper
label
pmid:36531020
[1] object · 3 fields
id
source:pmid:36531020
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manuscript
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PMID 36531020 full text
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id
data:geo:GSE161158
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GEO GSE161158
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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paper
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pmid:36531020
[1] object · 3 fields
id
source:pmid:36531020
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manuscript
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PMID 36531020 full text
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id
data:geo:GSE161158
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dataset
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GEO GSE161158
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agent:corpus-assay-engine
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extraction
used array · 1 item
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agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE161158
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used array · 1 item
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agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
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dsl_catalogue_fingerprint
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capability_table_fingerprint
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f2132e96ae6c7a4e
evidence array · 1 item
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Then, a univariate Cox proportional risk regression model was used to select candidate survival-related PRLs, and p< 0.01 was set as the threshold ( Supplementary Table S4 ). Then, the random survival forests-variable hunting (RSFVH) algorithm was used to further filter the genes.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36531020", "kind": "science-record", "revision": 3, "content_hash": "sha256:d81d5ed04f454d22c1bc0488cbf12f4c74e2106b0cde9053e7d6461dc4ce17e4", "created_at": "2026-11-01T19:01:03Z", "updated_at": "2026-11-01T22:08:21Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Pyroptosis-related lncRNAs: A novel prognosis signature of colorectal cancer.", "doi": "10.3389/fonc.2022.983895", "pmid": "36531020", "authors": ["Xing Cai", "Xiaoqing Liang", "Kun Wang", "Yin Liu", "Mengdi Hao", "Huimin Li", "Xiaofang Dai", "Lei Ding"], "journal": "Frontiers in oncology", "year": 2022, "abstract": "Pyroptosis is a newly discovered programmed cell death mechanism involved in tumorigenesis. Long non-coding RNAs (lncRNAs) have been implicated in colorectal cancer (CRC). However, the potential role of pyroptosis-related lncRNAs (PRLs) in CRC remains unelucidated. Therefore, we retrieved transcriptomic data of CRC patients from The Cancer Genome Atlas (TCGA). With the use of univariate and multivariate Cox proportional hazards regression models and the random forest algorithm, a new risk model was constructed based on eight PRLs: Z99289.2, FENDRR, CCDC144NL-ASL, TEX41, MNX1-AS1, NKILA, LINC02798, and LINC02381. Then, according to the Kaplan-Meier plots, the relationship of PRLs with the survival of CRC patients was explored and validated with our risk model in external datasets (Gene Expression Omnibus (GEO) databases; GEO17536, n = 177, and GSE161158, n = 250). To improve its clinical utility, a nomogram combining PRLs that could predict the clinical outcome of CRC patients was established. A full-spectrum immune landscape of CRC patients mediated by PRLs could be described. The PRLs were stratified into two molecular subtypes involved in immune modulators, immune infiltration of tumor immune microenvironment, and inflammatory pathways. Afterward, Tumor Immune Dysfunction and Exclusion (TIDE) and microsatellite instability (MSI) scores were analyzed. Three independent methods were applied to predict PRL-related sensitivity to chemotherapeutic drugs. Our comprehensive analysis of PRLs in CRC patients demonstrates a potential role of PRLs in predicting response to treatment and prognosis of CRC patients, which may provide a better understanding of molecular mechanisms underlying CRC pathogenesis and facilitate the development of effective immunotherapy.", "claims": [{"id": "claim-method", "statement": "Then, a univariate Cox proportional risk regression model was used to select candidate survival-related PRLs, and p< 0.01 was set as the threshold ( Supplementary Table S4 ). 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Further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The eight-PRL model predicted overall survival in the TCGA cohort with AUCs of 0.660, 0.768, and 0.734 at 1, 2, and 5 years, respectively, and its prognostic performance was supported in two external GEO cohorts.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36531020", "locator": "sections[11] \"Survival prediction performance of the model\" paragraph 2", "quote": "According to the ROC curves, PRLs might predict OS in TCGA cohort, with an AUC at 1, 2, and 5 years of 0.660, 0.768, and 0.734, respectively ( Figure 5C )."}, {"asset": "source:pmid:36531020", "locator": "sections[11] \"Survival prediction performance of the model\" paragraph 2", "quote": "Patients in the validation cohorts with a higher risk score had a lower survival rate compared to those with a low-risk score ( Figures 5D–I )."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The eight-PRL model predicted overall survival in the TCGA cohort with AUCs of 0.660, 0.768, and 0.734 at 1, 2, and 5 years, respectively, and its prognostic performance was supported in two external GEO cohorts.", "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:36531020"], "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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