甲基化
生物
癌症研究
DNA甲基化
生物标志物
肺癌
免疫系统
CpG站点
分子生物学
肿瘤科
基因表达
免疫学
医学
基因
遗传学
作者
Mingfang Zhang,Jing Li,Weibin Lin,Lin Qi,Caiyun Yao,Zhonghua Zheng,Chujia Chen,Shiwei Duan,Yuanlin Qi
出处
期刊:Genetic Testing and Molecular Biomarkers
[Mary Ann Liebert, Inc.]
日期:2022-08-01
卷期号:26 (7-8): 360-374
被引量:3
标识
DOI:10.1089/gtmb.2021.0305
摘要
Background: The importance of promoter methylation in non-small cell lung cancers (NSCLC) remains to be understood. Thus, we aimed to determine the diagnostic and prognostic value of the methylation of the endothelial PAS domain containing protein-1 (EPAS1) promoter in NSCLC. Methods:EPAS1 promoter methylation levels were quantitated by methylation-specific PCR. Further, we evaluated the expression, promoter methylation, prognostic value, and impact on immune cell infiltration of EPAS1 by analyzing the TCGA database using web-based bioinformatics tools including GEPIA, UALCAN and MethSurv. Results: Our results demonstrated that promoter methylation of EPAS1 downregulated its expression in NSCLC tissues. Additionally, an AUC value of 0.772 indicated that the methylation of the EPAS1 promoter is a potential diagnostic marker for NSCLC. A Kaplan-Meier analysis demonstrated that high methylation levels of CpG sites in the EPAS1 promoter were indicative of poorer overall survival. Further, EPAS1 expression levels were highly correlated with the infiltration of several types of immune cells, including γδ T cells, T follicular helper cells, CD8+ T cells, and CD4+ T-cells. Conclusion: Collectively, our findings suggest that methylation analyses of the EPAS1 promoter could be used as a prognostic biomarker for NSCLC and that EPAS1 potentially plays an important role in immune cell infiltration in NSCLC.
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