4.7 Article

Molecular Characterization, Tumor Microenvironment Association, and Drug Susceptibility of DNA Methylation-Driven Genes in Renal Cell Carcinoma

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.837919

关键词

renal cell carcinoma; molecular characterization; methylation-driven genes; tumor microenvironment; drug susceptibility

资金

  1. Scientific Research Project of Heilongjiang Provincial Health and Family Planning Commission [2017-070]
  2. Second Affiliated Hospital of Harbin Medical University First-class Discipline First-class Specialist Construction Project [100123]
  3. Harbin Medical University Scientific Research Innovation Fund [YJSKYCX2018-95HYD]

向作者/读者索取更多资源

DNA methylation plays a crucial role in the development of renal cell carcinoma (RCC). This study establishes molecular clusters and a prognostic model based on DNA methylation-driven genes, providing insights and tools for predicting and managing the prognosis of RCC patients.
Accumulating evidence suggests that DNA methylation has essential roles in the development of renal cell carcinoma (RCC). Aberrant DNA methylation acts as a vital role in RCC progression through regulating the gene expression, yet little is known about the role of methylation and its association with prognosis in RCC. The purpose of this study is to explore the DNA methylation-driven genes for establishing prognostic-related molecular clusters and providing a basis for survival prediction. In this study, 5,198 differentially expressed genes (DEGs) and 270 DNA methylation-driven genes were selected to obtain 146 differentially expressed DNA methylation-driven genes (DEMDGs). Two clusters were distinguished by consensus clustering using 146 DEMDGs. We further evaluated the immune status of two clusters and selected 106 DEGs in cluster 1. Cluster-based immune status analysis and functional enrichment analysis of 106 DEGs provide new insights for the development of RCC. To predict the prognosis of patients with RCC, a prognostic model based on eight DEMDGs was constructed. The patients were divided into high-risk groups and low-risk groups based on their risk scores. The predictive nomogram and the web-based survival rate calculator () were built to validate the predictive accuracy of the prognostic model. Gene set enrichment analysis was performed to annotate the signaling pathways in which the genes are enriched. The correlation of the risk score with clinical features, immune status, and drug susceptibility was also evaluated. These results suggested that the prognostic model might be a promising prognostic tool for RCC and might facilitate the management of patients with RCC.

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