鼻咽癌
生物
DNA甲基化
癌变
基因
甲基化
表观遗传学
抑制器
基因表达
癌症研究
抑癌基因
分子生物学
遗传学
医学
内科学
放射治疗
作者
Shuang Zhao,Ye Zhang,Xujun Liang,Maoyu Li,Fang Peng,Zhuchu Chen,Yongheng Chen
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2019-02-04
卷期号:19 (6): 772-782
被引量:2
标识
DOI:10.2174/1871520619666190204094815
摘要
DNA methylation, which acts as an expression regulator for multiple Tumor Suppressor Genes (TSGs), is believed to play an important role in Nasopharyngeal Carcinoma (NPC) development.We compared the effects of 5-aza-2-deoxycytidine (decitabine, DAC) on gene expression using RNA sequencing in NPC cells.We analyzed Differentially Expressed Genes (DEGs) in NPC cells using DAC demethylation treatment and found that 2182 genes were significantly upregulated (≥ 2-fold change), suggesting that they may play a key role in cell growth, proliferation, development, and death. For data analysis, we used the Gene Ontology database and pathway enrichment analysis of the DEGs to discover differential patterns of DNA methylation associated with changes in gene expression. Furthermore, we evaluated 74 methylated candidate TSGs from the DEGs in NPC cells and summarized these genes in several important signaling pathways frequently disrupted by promoter methylation in NPC tumorigenesis.Our study analyzes the DEGs and identifies a set of genes whose promoter methylation in NPC cells is reversed by DAC. These genes are potential substrates of DNMT inhibitors and may serve as tumor suppressors in NPC cells.
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