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pmid:35401564

A Novel m1A-Score Model Correlated With the Immune Microenvironment Predicts Prognosis in Hepatocellular Carcinoma.

Mingxing Zhao · Shen Shen · Chen Xue

Frontiers in immunology · 2022 doi:10.3389/fimmu.2022.805967

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Experiment

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Data

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Analysis

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pmid:35401564
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2026-11-01T18:14:13Z
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2026-11-01T22:48:48Z
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title
A Novel m1A-Score Model Correlated With the Immune Microenvironment Predicts Prognosis in Hepatocellular Carcinoma.
doi
10.3389/fimmu.2022.805967
pmid
35401564
authors array · 3 items
[0]
Mingxing Zhao
[1]
Shen Shen
[2]
Chen Xue
journal
Frontiers in immunology
year
2022
abstract
RNA methylation plays crucial roles in gene expression and has been indicated to be involved in tumorigenesis, while it is still unclear whether m1A modifications have potential roles in the prognosis of hepatocellular carcinoma (HCC). In this study, we comprehensively analyzed RNA sequencing (RNA-seq) data and clinical information using The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. We collected 10 m1A regulators and performed consensus clustering to determine m1A modification patterns in HCC. The CIBERSORT method was utilized to evaluate the level of immune cell infiltration. Principal component analysis was used to construct the m1A-score model. In the TCGA-LIHC cohort, the expression of all 10 m1A regulators was higher in tumor tissues than in normal control tissues, and 8 of 10 genes were closely related to the prognosis of HCC patients. Two distinct m1A methylation modification patterns (Clusters C1 and C2) were identified by the 10 regulators and were associated with different overall survival, TNM stage and tumor microenvironment (TME) characteristics. Based on the differentially expressed genes (DEGs) between C1 and C2, we identified three gene clusters (Clusters A, B and C). C1 with a better prognosis was mainly distributed in Cluster C, while Cluster A contained the fewest samples of C1. An m1A-score model was constructed using five m1A regulators related to prognosis. Patients with higher m1A scores showed a poorer prognosis than those with lower scores in the TCGA-LIHC and GSE14520 datasets. In conclusions, our study showed the vital role of m1A modification in the TME and progression of HCC. Quantitative evaluation of the m1A modification patterns of individual patients facilitates the development of more effective biomarkers for predicting the prognosis of patients with HCC.
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First, we identified the differentially expressed genes (DEGs) between distinct m1A clusters. The survival data and DEGs were analyzed by univariate Cox regression analysis. Second, least absolute shrinkage and selection operator (LASSO) Cox regression analysis was utilized to further narrow down the DEGs associated with prognosis. Finally, we performed multivariate Cox regression analysis to establish the prognostic model.
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sections[5] "Construction and Validation of a Prognostic Risk Model" paragraph 2
quote
First, we identified the differentially expressed genes (DEGs) between distinct m1A clusters. The survival data and DEGs were analyzed by univariate Cox regression analysis. Second, least absolute shrinkage and selection operator (LASSO) Cox regression analysis was utilized to further narrow down the DEGs associated with prognosis. Finally, we performed multivariate Cox regression analysis to establish the prognostic model.
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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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Patients with higher m1A scores showed a poorer prognosis than those with lower scores in the TCGA-LIHC and GSE14520 datasets.
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Patients with higher m1A scores showed a poorer prognosis than those with lower scores in the TCGA-LIHC and GSE14520 datasets.
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Patients with higher m1A scores showed a poorer prognosis than those with lower scores in the TCGA-LIHC and GSE14520 datasets.
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GSM712542
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488
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null
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null
platform
3921;571
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Homo sapiens
title
Gene expression data of human hepatocellular carcinoma (HCC)
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2026-11-01T15:39:54Z
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First, we identified the differentially expressed genes (DEGs) between distinct m1A clusters. The survival data and DEGs were analyzed by univariate Cox regression analysis. Second, least absolute shrinkage and selection operator (LASSO) Cox regression analysis was utilized to further narrow down the DEGs associated with prognosis. Finally, we performed multivariate Cox regression analysis to establish the prognostic model.
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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.
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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.
basis
The paper names GSE14520 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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minimax
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minimax
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2026-11-01T17:41:11Z
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data:geo:GSE14520
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GEO GSE14520
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we comprehensively analyzed RNA sequencing (RNA-seq) data and clinical information using The Can
[1]
. In this study, we comprehensively analyzed RNA sequencing (RNA-seq) data and clinical information usin
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e Academy of Sciences (Shanghai, China). The cell lines were maintained in Dulbecco’s modified Eagle’s medium (DMEM,
[1]
ll line L02 and human liver cancer cell line HepG2 were obtained from the Chinese Academy of Sc
[2]
H1, and ALKBH3) were highly expressed in the HepG2 cell line compared with the normal liver cel
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was not significantly different between the HepG2 and L02 cell lines ( Figure 1B ). Furthermor
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First, we identified the differentially expressed genes (DEGs) between distinct m1A clusters. The survival data and DEGs were analyzed by univariate Cox regression analysis. Second, least absolute shrinkage and selection operator (LASSO) Cox regression analysis was utilized to further narrow down the DEGs associated with prognosis. Finally, we performed multivariate Cox regression analysis to establish the prognostic model.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35401564", "kind": "science-record", "revision": 5, "content_hash": "sha256:9628bdb373570f07bb0d0e886ff66305aee09b6786dd0d528b6c9c84ee4675d2", "created_at": "2026-11-01T18:14:13Z", "updated_at": "2026-11-01T22:48:48Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A Novel m1A-Score Model Correlated With the Immune Microenvironment Predicts Prognosis in Hepatocellular Carcinoma.", "doi": "10.3389/fimmu.2022.805967", "pmid": "35401564", "authors": ["Mingxing Zhao", "Shen Shen", "Chen Xue"], "journal": "Frontiers in immunology", "year": 2022, "abstract": "RNA methylation plays crucial roles in gene expression and has been indicated to be involved in tumorigenesis, while it is still unclear whether m1A modifications have potential roles in the prognosis of hepatocellular carcinoma (HCC). In this study, we comprehensively analyzed RNA sequencing (RNA-seq) data and clinical information using The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. We collected 10 m1A regulators and performed consensus clustering to determine m1A modification patterns in HCC. The CIBERSORT method was utilized to evaluate the level of immune cell infiltration. Principal component analysis was used to construct the m1A-score model. In the TCGA-LIHC cohort, the expression of all 10 m1A regulators was higher in tumor tissues than in normal control tissues, and 8 of 10 genes were closely related to the prognosis of HCC patients. Two distinct m1A methylation modification patterns (Clusters C1 and C2) were identified by the 10 regulators and were associated with different overall survival, TNM stage and tumor microenvironment (TME) characteristics. Based on the differentially expressed genes (DEGs) between C1 and C2, we identified three gene clusters (Clusters A, B and C). C1 with a better prognosis was mainly distributed in Cluster C, while Cluster A contained the fewest samples of C1. An m1A-score model was constructed using five m1A regulators related to prognosis. Patients with higher m1A scores showed a poorer prognosis than those with lower scores in the TCGA-LIHC and GSE14520 datasets. In conclusions, our study showed the vital role of m1A modification in the TME and progression of HCC. Quantitative evaluation of the m1A modification patterns of individual patients facilitates the development of more effective biomarkers for predicting the prognosis of patients with HCC.", "claims": [{"id": "claim-method", "statement": "First, we identified the differentially expressed genes (DEGs) between distinct m1A clusters. The survival data and DEGs were analyzed by univariate Cox regression analysis. 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