DNA hypermethylation does not negatively impact the transcription of the TNF-α gene in an acute T-cell leukemia

被引:3
作者
Jayaraman, Arathi [1 ]
Jayaraman, Sundararajan [1 ]
机构
[1] Univ Illinois, Dept Med, Chicago, IL 60612 USA
关键词
CpG sites; decitabine; intragenic; leukemia; methylation; promoter; resveratrol; transcription; trichostatin A; tumor necrosis factor-alpha; TUMOR-NECROSIS-FACTOR; EPIGENETIC REGULATION; METHYLATION PROFILES; DEACETYLASES; EXPRESSION; INHIBITORS; RESVERATROL; CYTOKINE; PATTERNS; CANCER;
D O I
10.2217/epi-2019-0015
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aims: To better understand the roles of DNA methylation and histone acetylation in the transcription of the TNF-alpha gene (TNFA) in leukemic T cells. Materials & methods: Methylation levels of cytosine-guanosine dinucleotides (CPGs) were assessed by mass spectrometry. The influence of epigenetic modifiers on DNA methylation and TNFA transcription was also determined. Results: CPG at the 5' promoter region, first exon and first intron of TNFA were hypermethylated in leukemic T cells and not impacted by epigenetic drugs. Activation of the class III histone deacetylases but not inhibitors of DNA methylation or histone deacetylases repressed TNFA transcription. Conclusion: These results lend insights into the impact of epigenetic mechanisms on the TNFA transcription in leukemic T cells.
引用
收藏
页码:1753 / 1763
页数:11
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