Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics

Background Gastric cancer (GC) is a malignant tumor that originates from the epithelium of the gastric mucosa and has a poor prognosis. Stomach adenocarcinoma (STAD) covers 95% of total gastric cancer. This study aimed to identify the prognostic value of RNA methylation-related genes in gastric canc...

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Main Authors: Xionghui He, Xiang Chen, Changcheng Yang, Wei Wang, Hening Sun, Junjie Wang, Jincheng Fu, Huaying Dong
Format: Article
Language:English
Published: PeerJ Inc. 2024-02-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/16951.pdf
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author Xionghui He
Xiang Chen
Changcheng Yang
Wei Wang
Hening Sun
Junjie Wang
Jincheng Fu
Huaying Dong
author_facet Xionghui He
Xiang Chen
Changcheng Yang
Wei Wang
Hening Sun
Junjie Wang
Jincheng Fu
Huaying Dong
author_sort Xionghui He
collection DOAJ
description Background Gastric cancer (GC) is a malignant tumor that originates from the epithelium of the gastric mucosa and has a poor prognosis. Stomach adenocarcinoma (STAD) covers 95% of total gastric cancer. This study aimed to identify the prognostic value of RNA methylation-related genes in gastric cancer. Methods In this study, The Cancer Genome Atlas (TCGA)-STAD and GSE84426 cohorts were downloaded from public databases. Patients were classified by consistent cluster analysis based on prognosis-related differentially expressed RNA methylation genes Prognostic genes were obtained by differential expression, univariate Cox and least absolute shrinkage and selection operator (LASSO) analyses. The prognostic model was established and validated in the training set, test set and validation set respectively. Independent prognostic analysis was implemented. Finally, the expression of prognostic genes was affirmed by reverse transcription quantitative PCR (RT-qPCR). Results In total, four prognostic genes (ACTA2, SAPCD2, PDK4 and APOD) related to RNA methylation were identified and enrolled into the risk signature. The STAD patients were divided into high- and low-risk groups based on the medium value of the risk score, and patients in the high-risk group had a poor prognosis. In addition, the RNA methylation-relevant risk signature was validated in the test and validation sets, and was authenticated as a reliable independent prognostic predictor. The nomogram was constructed based on the independent predictors to predict the 1/3/5-year survival probability of STAD patients. The gene set enrichment analysis (GSEA) result suggested that the poor prognosis in the high-risk subgroup may be related to immune-related pathways. Finally, the experimental results indicated that the expression trends of RNA methylation-relevant prognostic genes in gastric cancer cells were in agreement with the result of bioinformatics. Conclusion Our study established a novel RNA methylation-related risk signature for STAD, which was of considerable significance for improving prognosis of STAD patients and offering theoretical support for clinical therapy.
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spelling doaj.art-93bb6f2d25314c67aba0b4369e65f1bc2024-03-02T15:05:27ZengPeerJ Inc.PeerJ2167-83592024-02-0112e1695110.7717/peerj.16951Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformaticsXionghui He0Xiang Chen1Changcheng Yang2Wei Wang3Hening Sun4Junjie Wang5Jincheng Fu6Huaying Dong7Department of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of Medical Oncology, The First Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaDepartment of General Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Hainan Medical College, HaiNan, HaiKou, ChinaBackground Gastric cancer (GC) is a malignant tumor that originates from the epithelium of the gastric mucosa and has a poor prognosis. Stomach adenocarcinoma (STAD) covers 95% of total gastric cancer. This study aimed to identify the prognostic value of RNA methylation-related genes in gastric cancer. Methods In this study, The Cancer Genome Atlas (TCGA)-STAD and GSE84426 cohorts were downloaded from public databases. Patients were classified by consistent cluster analysis based on prognosis-related differentially expressed RNA methylation genes Prognostic genes were obtained by differential expression, univariate Cox and least absolute shrinkage and selection operator (LASSO) analyses. The prognostic model was established and validated in the training set, test set and validation set respectively. Independent prognostic analysis was implemented. Finally, the expression of prognostic genes was affirmed by reverse transcription quantitative PCR (RT-qPCR). Results In total, four prognostic genes (ACTA2, SAPCD2, PDK4 and APOD) related to RNA methylation were identified and enrolled into the risk signature. The STAD patients were divided into high- and low-risk groups based on the medium value of the risk score, and patients in the high-risk group had a poor prognosis. In addition, the RNA methylation-relevant risk signature was validated in the test and validation sets, and was authenticated as a reliable independent prognostic predictor. The nomogram was constructed based on the independent predictors to predict the 1/3/5-year survival probability of STAD patients. The gene set enrichment analysis (GSEA) result suggested that the poor prognosis in the high-risk subgroup may be related to immune-related pathways. Finally, the experimental results indicated that the expression trends of RNA methylation-relevant prognostic genes in gastric cancer cells were in agreement with the result of bioinformatics. Conclusion Our study established a novel RNA methylation-related risk signature for STAD, which was of considerable significance for improving prognosis of STAD patients and offering theoretical support for clinical therapy.https://peerj.com/articles/16951.pdfStomach adenocarcinomaRNA methylationRisk modelImmune microenvironmentBioinformatics
spellingShingle Xionghui He
Xiang Chen
Changcheng Yang
Wei Wang
Hening Sun
Junjie Wang
Jincheng Fu
Huaying Dong
Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
PeerJ
Stomach adenocarcinoma
RNA methylation
Risk model
Immune microenvironment
Bioinformatics
title Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
title_full Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
title_fullStr Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
title_full_unstemmed Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
title_short Prognostic value of RNA methylation-related genes in gastric adenocarcinoma based on bioinformatics
title_sort prognostic value of rna methylation related genes in gastric adenocarcinoma based on bioinformatics
topic Stomach adenocarcinoma
RNA methylation
Risk model
Immune microenvironment
Bioinformatics
url https://peerj.com/articles/16951.pdf
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