4.5 Article

EZH2 is a potential prognostic predictor of glioma

期刊

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
卷 25, 期 2, 页码 925-936

出版社

WILEY
DOI: 10.1111/jcmm.16149

关键词

EZH2; glioma; immunity; overall survival

资金

  1. Fundamental Research Funds for the Central Universities [WK9110000069, WK9110000035, WK9110000032]
  2. Anhui Provincial Natural Science Foundation [1808085QH287]
  3. Science and Technology Project grant from Anhui Province [1508085QH184, 201904a07020098]
  4. National Natural Science Foundation of China [81803041]

向作者/读者索取更多资源

The study found that the expression of EZH2 in glioma is significantly correlated with clinicopathologic characteristics and overall survival rate, suggesting its potential as a prognostic molecular marker. Additionally, the research identified associations between EZH2 and signaling pathways related to the cell cycle, DNA replication, and immune checkpoints.
The enhancer of zeste homologue 2 (EZH2) is a histone H3 lysine 27 methyltransferase that promotes tumorigenesis in a variety of human malignancies by altering the expression of tumour suppressor genes. To evaluate the prognostic value of EZH2 in glioma, we analysed gene expression data and corresponding clinicopathological information from the Chinese Glioma Genome Atlas, the Cancer Genome Atlas and GTEx. Increased expression of EZH2 was significantly associated with clinicopathologic characteristics and overall survival as evaluated by univariate and multivariate Cox regression. Gene Set Enrichment Analysis revealed an association of EZH2 expression with the cell cycle, DNA replication, mismatch repair, p53 signalling and pyrimidine metabolism. We constructed a nomogram for prognosis prediction with EZH2, clinicopathologic variables and significantly correlated genes. EZH2 was demonstrated to be significantly associated with several immune checkpoints and tumour-infiltrating lymphocytes. Furthermore, the ESTIMATE and Timer Database scores indicated correlation of EZH2 expression with a more immunosuppressive microenvironment for glioblastoma than for low grade glioma. Overall, our study demonstrates that expression of EZH2 is a potential prognostic molecular marker of poor survival in glioma and identifies signalling pathways and immune checkpoints regulated by EHZ2, suggesting a direction for future application of immune therapy in glioma.

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