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pmid:35309906

Prognostic Value of Genomic Instability of m6A-Related lncRNAs in Lung Adenocarcinoma.

Rui Li · Jian-Ping Li · Ting-Ting Liu · Chen Huo · Jie Yao · Xiu-Li Ji · Yi-Qing Qu

Frontiers in cell and developmental biology · 2022 doi:10.3389/fcell.2022.707405

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Experiment

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Data

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Analysis

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title
Prognostic Value of Genomic Instability of m6A-Related lncRNAs in Lung Adenocarcinoma.
doi
10.3389/fcell.2022.707405
pmid
35309906
authors array · 7 items
[0]
Rui Li
[1]
Jian-Ping Li
[2]
Ting-Ting Liu
[3]
Chen Huo
[4]
Jie Yao
[5]
Xiu-Li Ji
[6]
Yi-Qing Qu
journal
Frontiers in cell and developmental biology
year
2022
abstract
Background: Genomic instability of N6-methyladenosine (m6A)-related long noncoding RNAs (lncRNAs) plays a pivotal role in the tumorigenesis of lung adenocarcinoma (LUAD). Our study identified a signature of genomic instability of m6A-associated lncRNA signature and revealed its prognostic role in LUAD. Methods: We downloaded RNA-sequencing data and somatic mutation data for LUAD from The Cancer Genome Atlas (TCGA) and the GSE102287 dataset from the Gene Expression Omnibus (GEO) database. The "Limma" R package was used to identify a network of regulatory m6A-related lncRNAs. We used the Wilcoxon test method to identify genomic-instability-derived m6A-related lncRNAs. A competing endogenous RNA (ceRNA) network was constructed to identify the mechanism of the genomic instability of m6A-related lncRNAs. Univariate and multivariate Cox regression analyses were performed to construct a prognostic model for internal testing and validation of the prognostic m6A-related lncRNAs using the GEO dataset. Performance analysis was conducted to compare our prognostic model with the previously published lncRNA models. The CIBERSORT algorithm was used to explore the relationship of m6A-related lncRNAs and the immune microenvironment. Prognostic m6A-related lncRNAs in prognosis, the tumor microenvironment, stemness scores, and anticancer drug sensitivity were analyzed to explore the role of prognostic m6A-related lncRNAs in LUAD. Results: A total of 42 genomic instability-derived m6A-related lncRNAs were differentially expressed between the GS (genomic stable) and GU (genomic unstable) groups of LUAD patients. Four differentially expressed lncRNAs, 17 differentially expressed microRNAs, and 75 differentially expressed mRNAs were involved in the genomic-instability-derived m6A-related lncRNA-mediated ceRNA network. A prediction model based on 17 prognostic m6A-associated lncRNAs was constructed based on three TCGA datasets (all, training, and testing) and validated in the GSE102287 dataset. Performance comparison analysis showed that our prediction model (area under the curve [AUC] = 0.746) could better predict the survival of LUAD patients than the previously published lncRNA models (AUC = 0.577, AUC = 0.681). Prognostic m6A-related-lncRNAs have pivotal roles in the tumor microenvironment, stemness scores, and anticancer drug sensitivity of LUAD. Conclusion: A signature of genomic instability of m6A-associated lncRNAs to predict the survival of LUAD patients was validated. The prognostic, immune microenvironment and anticancer drug sensitivity analysis shed new light on the potential novel therapeutic targets in LUAD.
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The 17-prognostic-m6A-associated-lncRNA model achieved an AUC of 0.746 and outperformed the two previously published lncRNA signatures.
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Performance comparison analysis showed that our prediction model (area under the curve [AUC] = 0.746) could better predict the survival of LUAD patients than the previously published lncRNA models (AUC = 0.577, AUC = 0.681).
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sha256:65a98a5567eea9b3989208150616289e12751e208d784cf1f4153fe42d42353a
fork_of
null
gaps array · 8 items
[0]
asset:data:geo:GSE102287 licence not read
[1]
asset:data:geo:GSE102287 not downloaded
[2]
execution.not_run
[3]
method.group_comparison_wilcoxon
[4]
review.human_critique
[5]
review.independent_reader
[6]
review.machine_critique
[7]
step:run_analysis blocked on method:group_comparison_wilcoxon
assays array · 3 items
[0] object · 11 fields
role
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definition_id
microarray
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99e1195c7d6f
required_operations array · 0 items
support_state
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source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.93
evidence array · 1 item
[0]
he fraction of 22 immune cell types from six microarray public datasets based on the expression file
order_basis
paper_text_order:3032
id
assay:1
[1] object · 11 fields
role
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99e1195c7d6f
required_operations array · 0 items
support_state
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source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 3 items
[0]
ang Biotechnology Co., Ltd. Human LUAD cells A549, H1299, and H1975 were purchased from Procel
[1]
and penicillin/streptomycin (100 mg/ml), and A549, H1299, and H1975 were cultivated in RPMI-16
[2]
R software. Significant differences between A549, H1299, H1975, and Beas-2B cell were evaluat
order_basis
paper_text_order:3602
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assay:2
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group_comparison
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f2132e96ae6c7a4e
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f2132e96ae6c7a4e
evidence array · 1 item
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Wilcoxon
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id
assay:3
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35309906", "kind": "science-record", "revision": 4, "content_hash": "sha256:1ca00c58bed1b977f605c2c887d289c733d3a091bdf46f0f1082169dac2048cc", "created_at": "2026-11-01T18:14:06Z", "updated_at": "2026-11-01T22:06:09Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic Value of Genomic Instability of m6A-Related lncRNAs in Lung Adenocarcinoma.", "doi": "10.3389/fcell.2022.707405", "pmid": "35309906", "authors": ["Rui Li", "Jian-Ping Li", "Ting-Ting Liu", "Chen Huo", "Jie Yao", "Xiu-Li Ji", "Yi-Qing Qu"], "journal": "Frontiers in cell and developmental biology", "year": 2022, "abstract": "Background: Genomic instability of N6-methyladenosine (m6A)-related long noncoding RNAs (lncRNAs) plays a pivotal role in the tumorigenesis of lung adenocarcinoma (LUAD). Our study identified a signature of genomic instability of m6A-associated lncRNA signature and revealed its prognostic role in LUAD. Methods: We downloaded RNA-sequencing data and somatic mutation data for LUAD from The Cancer Genome Atlas (TCGA) and the GSE102287 dataset from the Gene Expression Omnibus (GEO) database. The \"Limma\" R package was used to identify a network of regulatory m6A-related lncRNAs. We used the Wilcoxon test method to identify genomic-instability-derived m6A-related lncRNAs. A competing endogenous RNA (ceRNA) network was constructed to identify the mechanism of the genomic instability of m6A-related lncRNAs. Univariate and multivariate Cox regression analyses were performed to construct a prognostic model for internal testing and validation of the prognostic m6A-related lncRNAs using the GEO dataset. Performance analysis was conducted to compare our prognostic model with the previously published lncRNA models. The CIBERSORT algorithm was used to explore the relationship of m6A-related lncRNAs and the immune microenvironment. Prognostic m6A-related lncRNAs in prognosis, the tumor microenvironment, stemness scores, and anticancer drug sensitivity were analyzed to explore the role of prognostic m6A-related lncRNAs in LUAD. Results: A total of 42 genomic instability-derived m6A-related lncRNAs were differentially expressed between the GS (genomic stable) and GU (genomic unstable) groups of LUAD patients. Four differentially expressed lncRNAs, 17 differentially expressed microRNAs, and 75 differentially expressed mRNAs were involved in the genomic-instability-derived m6A-related lncRNA-mediated ceRNA network. A prediction model based on 17 prognostic m6A-associated lncRNAs was constructed based on three TCGA datasets (all, training, and testing) and validated in the GSE102287 dataset. Performance comparison analysis showed that our prediction model (area under the curve [AUC] = 0.746) could better predict the survival of LUAD patients than the previously published lncRNA models (AUC = 0.577, AUC = 0.681). Prognostic m6A-related-lncRNAs have pivotal roles in the tumor microenvironment, stemness scores, and anticancer drug sensitivity of LUAD. Conclusion: A signature of genomic instability of m6A-associated lncRNAs to predict the survival of LUAD patients was validated. The prognostic, immune microenvironment and anticancer drug sensitivity analysis shed new light on the potential novel therapeutic targets in LUAD.", "claims": [{"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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