Identification of aberrantly methylated differentially expressed genes targeted by differentially expressed miRNA in osteosarcoma
Autor: | Ridong Liang, Zhi-Fei Cui, Wen-Le Tan, Hai Lu, Ting-Xuan Wang, Jincheng Huang, Qingchu Li |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
PYCARD General Medicine Methylation Biology medicine.disease Metastasis law.invention 03 medical and health sciences 030104 developmental biology 0302 clinical medicine law 030220 oncology & carcinogenesis DNA methylation microRNA medicine Cancer research Osteosarcoma Suppressor Original Article Gene |
Zdroj: | Ann Transl Med |
ISSN: | 2305-5839 |
Popis: | Background Osteosarcoma (OS) is the most common primary bone tumors diagnosed in children and adolescents. Recent studies have shown a prognostic role of DNA methylation in various cancers, including OS. The aim of this study was to identify the aberrantly methylated genes that are prognostically relevant in OS. Methods The differentially expressed mRNAs, miRNAs and methylated genes (DEGs, DEMs and DMGs respectively) were screened from various GEO databases, and the potential target genes of the DEMs were predicted by the RNA22 program. The protein-protein interaction (PPI) networks were constructed using the STRING database and visualized by Cytoscape software. The functional enrichment and survival analyses of the screened genes was performed using the R software. Results Forty-seven downregulated hypermethylated genes and three upregulated hypomethylated genes were identified that were enriched in cell activation, migration and proliferation functions, and were involved in cancer-related pathways like JAK-STAT and PI3K-AKT. Eight downregulated hypermethylated tumor suppressor genes (TSGs) were identified among the screened genes based on the TSGene database. These hub genes are likely involved in OS genesis, progression and metastasis, and are potential prognostic biomarkers and therapeutic targets. Conclusions TSGs including PYCARD, STAT5A, CXCL12 and CXCL14 were aberrantly methylated in OS, and are potential prognostic biomarkers and therapeutic targets. Our findings provide new insights into the role of methylation in OS progression. |
Databáze: | OpenAIRE |
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