Journal of Capital Medical University ›› 2022, Vol. 43 ›› Issue (1): 113-119.doi: 10.3969/j.issn.1006-7795.2022.01.019

• Basic Research • Previous Articles     Next Articles

Identification of protein-coding genes regulated by differential DNA methylation enhancer regions in glioblastoma

Zhao Xiaoxiao1,2, Yu Qiuhong3*, Ji Jianghuai4,5, Wang Shijia1,2, Wang Rendong1,2, Li Dongguo1,2*   

  1. 1. School of Biomedical Engineering, Capital Medical University, Beijing 100069, China;
    2. Beijing Key Laboratory of Fundamental Research on Biomechanics in Clinical, Capital Medical University, Beijing 100069, China;
    3. Department of Hyperbaric Oxygen, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China;
    4. Department of Radiation Physics Zhejiang Cancer Hospital, Hangzhou 310022,China;
    5. Zhejiang Key Laboratory of Radiation Oncology, Hangzhou 310022, China
  • Received:2021-07-06 Online:2022-02-21 Published:2022-01-27
  • Contact: * E-mail:yuqiuhong@bjtth.org;dg213@ccmu.edu.cn

Abstract: Objective By integrating and analyzing DNA methylation data and expression data in glioblastoma (GBM), we identified protein-coding genes (PCGs) that might be regulated by differential DNA methylation enhancer regions (DMERs) in GBM, predicted the biological functions of PCGs regulated by DMERs in GBM, and explored the potential biomarkers related to the GBM prognosis. Methods Based on methylation data and expression data in public disease databases, we used a computational strategy to construct genome-wide enhancer regions and screened for DMERS in GBM. We identified PCGs whose expression might be regulated by DMERs and performed enrichment analysis on these PCGs. Based on the patient's clinical information and the expression data of the corresponding samples, we performed Kaplan-Meier prognostic analysis on the identified PCGs. Results We screened 16 287 DMERs and identified 795 pairs of DMER-PCGs in this study, including 593 hypomethylated enhancers, 82 hypermethylated enhancers and 642 PCGs. We excavated 45 PCGs that were significantly related to the overall survival of GBM. Conclusion This study has further deepened the understanding of the regulatory pattern of enhancer methylation in GBM, and provided assistance for the development of novel biomarkers and targets for diagnosis and treatment of GBM.

Key words: glioblastoma, DNA methylation, enhancer region, epigenetic regulation, risk markers

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