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pmid:35785179

Construction of a Novel Prognostic Model in Lung Adenocarcinoma Based on 7-Methylguanosine-Related Gene Signatures.

Fei Lu · Jingyan Gao · Yu Hou · Ke Cao · Yaoxiong Xia · Zhengting Chen · Hui Yu · Li Chang · Wenhui Li

Frontiers in oncology · 2022 doi:10.3389/fonc.2022.876360

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Experiment

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Data

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pmid:35785179
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2026-11-01T18:14:49Z
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title
Construction of a Novel Prognostic Model in Lung Adenocarcinoma Based on 7-Methylguanosine-Related Gene Signatures.
doi
10.3389/fonc.2022.876360
pmid
35785179
authors array · 9 items
[0]
Fei Lu
[1]
Jingyan Gao
[2]
Yu Hou
[3]
Ke Cao
[4]
Yaoxiong Xia
[5]
Zhengting Chen
[6]
Hui Yu
[7]
Li Chang
[8]
Wenhui Li
journal
Frontiers in oncology
year
2022
abstract
Increasing evidence has implicated the modification of 7-methylguanosine (m7G), a type of RNA modification, in tumor progression. However, no comprehensive analysis to date has summarized the predicted role of m7G-related gene signatures in lung adenocarcinoma (LUAD). Herein, we aimed to develop a novel prognostic model in LUAD based on m7G-related gene signatures. The LUAD transcriptome profiling data and corresponding clinical data were acquired from the Cancer Genome Atlas (TCGA) and two Gene Expression Omnibus datasets. After screening, we first obtained 29 m7G-related genes, most of which were upregulated in tumor tissues and negatively associated with overall survival (OS). According to the expression similarity of m7G-related genes, the combined samples from the TCGA-LUAD and GSE68465 datasets were further classified as two clusters that exhibit distinct OS rates and genetic heterogeneity. Then, we constructed a novel prognostic model involving four genes by using 130 differentially expressed genes among the two clusters. The combined samples were randomly divided into a training cohort and an internal validation cohort in a 1:1 ratio, and the GSE72094 dataset was used as an external validation cohort. The samples were divided into high- and low-risk groups. We demonstrated that a higher risk score was an independent negative prognostic factor and predicted poor OS. A nomogram was further constructed to better predict the survival of LUAD patients. Functional enrichment analyses indicated that cell cycle and DNA replication-related biological processes and pathways were enriched in the high-risk group. More importantly, the low-risk group had greater infiltration and enrichment of most immune cells, as well as higher ESTIMATE, immune, and stromal scores. In addition, the high-risk group had a lower TIDE score and higher expressions of most immune checkpoint-related genes. We finally noticed that patients in the high-risk group were more sensitive to chemotherapeutic agents commonly used in LUAD. In conclusion, we herein summarized for the first time the alterations and prognostic role of m7G-related genes in LUAD and then constructed a prognostic model based on m7G-related gene signatures that could accurately and stably predict survival and guide individualized treatment decision-making in LUAD patients.
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Subsequently, univariate Cox analysis was applied to explore the prognosis-related DEGs. Then, we used the LASSO regression with 10-fold cross-validation to narrow down the prognosis-related DEGs applying the R package “glmnet,” and further performed the multivariate Cox regression analysis to establish a signature for evaluating the relationships between the DEGs and the survival of LUAD patients.
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sections[9] "Construction and Validation of a Prognostic Model" paragraph 2
quote
Subsequently, univariate Cox analysis was applied to explore the prognosis-related DEGs. Then, we used the LASSO regression with 10-fold cross-validation to narrow down the prognosis-related DEGs applying the R package “glmnet,” and further performed the multivariate Cox regression analysis to establish a signature for evaluating the relationships between the DEGs and the survival of LUAD patients.
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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[25] "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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A four-gene prognostic model comprising KIF20B, HMMR, ARNTL2, and DKK1 was constructed and validated for predicting survival in LUAD; in the training cohort, its 1-, 2-, and 3-year AUC values were 0.734, 0.691, and 0.676, respectively.
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sections[19] "Construction and Validation of a Novel Prognostic Model Based on DEGs Between Clusters" paragraph 2
quote
In the training cohort, the AUC values of the present risk model were 0.734, 0.691, and 0.676 for the 1-, 2-, and 3-year prognoses, respectively ( Figure 5G ), with similar results observed in the internal and external validation groups ( Figures 5H, I ).
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A four-gene prognostic model comprising KIF20B, HMMR, ARNTL2, and DKK1 was constructed and validated for predicting survival in LUAD; in the training cohort, its 1-, 2-, and 3-year AUC values were 0.734, 0.691, and 0.676, respectively.
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96
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Homo sapiens
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caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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[2] object · 15 fields
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data:geo:GSE72094
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note
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
structure object · 15 fields
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GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
access_statement_kind
data_availability_statement
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null
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15048
taxon
Homo sapiens
title
KRAS mutation-associated gene expression, p53 and STK11 mutations, proliferation and immune surveillance in lung adenocarcinoma
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[0]
asset:data:geo:GSE68465 not downloaded
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[2]
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[3]
asset:data:geo:GSE72094 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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[0]
cox_ph
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parameters object · 0 fields
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[0]
time_to_event_with_censoring
evidence object · 3 fields
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quote
Subsequently, univariate Cox analysis was applied to explore the prognosis-related DEGs. Then, we used the LASSO regression with 10-fold cross-validation to narrow down the prognosis-related DEGs applying the R package “glmnet,” and further performed the multivariate Cox regression analysis to establish a signature for evaluating the relationships between the DEGs and the survival of LUAD patients.
[1] object · 10 fields
id
method-2
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network_analysis
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[0]
build_graph
[1]
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[2]
pathway_enrich
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[0]
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evidence object · 3 fields
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0.8
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quote
PPI
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complete
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[0] object · 6 fields
capability_id
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[8]
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Automated Assays Laravel application and simulated adapters
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complete
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cox_ph
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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
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R1
capability_id
capability:computational_analysis
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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]
GSE68465
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GSE72094
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[0]
GSE68465
[1]
GSE72094
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 GSE68465, GSE72094 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
[0]
cox_ph
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[0]
source:pmid:35785179
[1]
data:geo:GSE68465
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[0]
run_analysis
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[0]
data:geo:GSE68465
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T17:53:36Z
independence
single_reader
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verbatim
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verbatim
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5
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18913
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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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minimax
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[1]
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[2]
review.human_critique
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not_run
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null
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[0]
execution.not_run
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pmid:35785179
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paper
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pmid:35785179
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source:pmid:35785179
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manuscript
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PMID 35785179 full text
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data:geo:GSE68465
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dataset
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GEO GSE68465
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
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classification
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pmid:35785179
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paper
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pmid:35785179
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source:pmid:35785179
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PMID 35785179 full text
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data:geo:GSE68465
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dataset
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GEO GSE68465
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agent:corpus-assay-engine
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activity-read-35785179
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extraction
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[0]
source:pmid:35785179
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agent:minimax-reader
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activity-resolve-GSE68465
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accession_resolution
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[0]
data:geo:GSE68465
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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lineage object · 4 fields
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pmid:35785179
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Subsequently, univariate Cox analysis was applied to explore the prognosis-related DEGs. Then, we used the LASSO regression with 10-fold cross-validation to narrow down the prognosis-related DEGs applying the R package “glmnet,” and further performed the multivariate Cox regression analysis to establish a signature for evaluating the relationships between the DEGs and the survival of LUAD patients.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35785179", "kind": "science-record", "revision": 4, "content_hash": "sha256:e6500fb7ecb70e8d42c826fa3f7e4e50508c54566047750ab485fdf50ad4243d", "created_at": "2026-11-01T18:14:49Z", "updated_at": "2026-11-01T22:06:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction of a Novel Prognostic Model in Lung Adenocarcinoma Based on 7-Methylguanosine-Related Gene Signatures.", "doi": "10.3389/fonc.2022.876360", "pmid": "35785179", "authors": ["Fei Lu", "Jingyan Gao", "Yu Hou", "Ke Cao", "Yaoxiong Xia", "Zhengting Chen", "Hui Yu", "Li Chang", "Wenhui Li"], "journal": "Frontiers in oncology", "year": 2022, "abstract": "Increasing evidence has implicated the modification of 7-methylguanosine (m7G), a type of RNA modification, in tumor progression. However, no comprehensive analysis to date has summarized the predicted role of m7G-related gene signatures in lung adenocarcinoma (LUAD). Herein, we aimed to develop a novel prognostic model in LUAD based on m7G-related gene signatures. The LUAD transcriptome profiling data and corresponding clinical data were acquired from the Cancer Genome Atlas (TCGA) and two Gene Expression Omnibus datasets. After screening, we first obtained 29 m7G-related genes, most of which were upregulated in tumor tissues and negatively associated with overall survival (OS). According to the expression similarity of m7G-related genes, the combined samples from the TCGA-LUAD and GSE68465 datasets were further classified as two clusters that exhibit distinct OS rates and genetic heterogeneity. Then, we constructed a novel prognostic model involving four genes by using 130 differentially expressed genes among the two clusters. The combined samples were randomly divided into a training cohort and an internal validation cohort in a 1:1 ratio, and the GSE72094 dataset was used as an external validation cohort. The samples were divided into high- and low-risk groups. We demonstrated that a higher risk score was an independent negative prognostic factor and predicted poor OS. A nomogram was further constructed to better predict the survival of LUAD patients. Functional enrichment analyses indicated that cell cycle and DNA replication-related biological processes and pathways were enriched in the high-risk group. More importantly, the low-risk group had greater infiltration and enrichment of most immune cells, as well as higher ESTIMATE, immune, and stromal scores. In addition, the high-risk group had a lower TIDE score and higher expressions of most immune checkpoint-related genes. We finally noticed that patients in the high-risk group were more sensitive to chemotherapeutic agents commonly used in LUAD. In conclusion, we herein summarized for the first time the alterations and prognostic role of m7G-related genes in LUAD and then constructed a prognostic model based on m7G-related gene signatures that could accurately and stably predict survival and guide individualized treatment decision-making in LUAD patients.", "claims": [{"id": "claim-method", "statement": "Subsequently, univariate Cox analysis was applied to explore the prognosis-related DEGs. 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Further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A four-gene prognostic model comprising KIF20B, HMMR, ARNTL2, and DKK1 was constructed and validated for predicting survival in LUAD; in the training cohort, its 1-, 2-, and 3-year AUC values were 0.734, 0.691, and 0.676, respectively.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35785179", "locator": "sections[19] \"Construction and Validation of a Novel Prognostic Model Based on DEGs Between Clusters\" paragraph 2", "quote": "In the training cohort, the AUC values of the present risk model were 0.734, 0.691, and 0.676 for the 1-, 2-, and 3-year prognoses, respectively ( Figure 5G ), with similar results observed in the internal and external validation groups ( Figures 5H, I )."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A four-gene prognostic model comprising KIF20B, HMMR, ARNTL2, and DKK1 was constructed and validated for predicting survival in LUAD; in the training cohort, its 1-, 2-, and 3-year AUC values were 0.734, 0.691, and 0.676, respectively.", "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:35785179"], "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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