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pmid:36397411

Potential impact of WTAP and YTHDF2 on tumor immunity in lung adenocarcinoma.

Xinyu Zhang · Xinsheng Cai

Medicine · 2022 doi:10.1097/MD.0000000000031195

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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pmid:36397411
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2026-11-01T19:00:51Z
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title
Potential impact of WTAP and YTHDF2 on tumor immunity in lung adenocarcinoma.
doi
10.1097/MD.0000000000031195
pmid
36397411
authors array · 2 items
[0]
Xinyu Zhang
[1]
Xinsheng Cai
journal
Medicine
year
2022
abstract
WTAP and N6-methyladenosine (m6A) reader proteins (YTHDF2) are N6-methyladenosine (m6A) methyltransferase and m6A reading proteins, respectively. In recent years, the tumor immune environment has received more and more attention in the progress and treatment of cancer. The aim of this study was to investigate the relationship between N6-methyladenosine (m6A) methyltransferase (WTAP)/YTHDF2 and the immunological characteristics of lung adenocarcinoma (LUAD). Based on the expression of WTAP and YTHDF2 in the cancer genome atlas (TCGA) and gene expression omnibus (GEO) database, LUAD patients were divided into 2 clusters by coherently clustering method, and performed gene set enrichment analysis (GSEA) to identify the functional differences. Immunoinvasion analysis was performed using ESTIMATE, CIBERSORT, and single-sample GSEA (ssGSEA), and expression of immune checkpoint inhibitors (ICIs) targets was assessed, while tumor mutation burden (TMB) was calculated in tumor samples. Weighted gene co-expression network analysis (WGCNA) was used to identify the genes related to both WTAP/YTHDF2 expression and immunity. The immunological characteristics between the 2 clusters were externally verified based on GSE39582. The expression of WTAP was higher in cluster 1 and YTHDF2 was lower, but it was opposite in cluster 2. Cluster 1 had stronger immune infiltration, more ICIs target expression, more TMB. In addition, WGCNA identified 22 genes associated with WTAP/YTHDF2 expression and immune score, including TIM3 (HAVCR2) and CD86. WTAP and YTHDF2 influence immune contexture and may be novel prognostic and druggable targets associated with the immune system of LUAD.
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Box plot analysis was performed using Wilcoxon rank sum test. Correlation analysis was performed using Spearman’s correlation analysis.
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Cluster 1 had stronger immune infiltration, more ICI-target expression, and higher tumor mutational burden than cluster 2.
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Cluster 1 had stronger immune infiltration, more ICIs target expression, more TMB.
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Cluster 1 had stronger immune infiltration, more ICI-target expression, and higher tumor mutational burden than cluster 2.
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Box plot analysis was performed using Wilcoxon rank sum test. Correlation analysis was performed using Spearman’s correlation analysis.
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evidence object · 3 fields
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: wilcoxon.
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The datasets generated during and/or analyzed during the current study are publicly available.
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The paper names GSE68465 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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or tumor tissues versus normal tissues using transcriptomic data from TCGA-LUAD; WTAP and YTHDF2 were di
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Complete file
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The aim of this study was to investigate the relationship between N6-methyladenosine (m6A) methyltransferase (WTAP)/YTHDF2 and the immunological characteristics of lung adenocarcinoma (LUAD). Based on the expression of WTAP and YTHDF2 in the cancer genome atlas (TCGA) and gene expression omnibus (GEO) database, LUAD patients were divided into 2 clusters by coherently clustering method, and performed gene set enrichment analysis (GSEA) to identify the functional differences. Immunoinvasion analysis was performed using ESTIMATE, CIBERSORT, and single-sample GSEA (ssGSEA), and expression of immune checkpoint inhibitors (ICIs) targets was assessed, while tumor mutation burden (TMB) was calculated in tumor samples. Weighted gene co-expression network analysis (WGCNA) was used to identify the genes related to both WTAP/YTHDF2 expression and immunity. The immunological characteristics between the 2 clusters were externally verified based on GSE39582. 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