DNA methylation microarray-based screening of epigenetically masked genes in patients with anti-tuberculosis drug-induced liver injury
Clinical Medicine|更新时间:2026-01-09
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DNA methylation microarray-based screening of epigenetically masked genes in patients with anti-tuberculosis drug-induced liver injury
Journal of Third Military Medical UniversityVol. 41, Issue 4, Pages: 353-359(2019)
作者机构:
1.063210 河北 唐山, 华北理工大学公共卫生学院,河北省煤矿卫生与安全重点实验室
2.162650 内蒙古 呼伦贝尔,呼伦贝尔市传染病医院检验科
作者简介:
基金信息:
National Natural Science Foundation of China(81670525);Graduate Student Innovation Fund of North China University of Science and Technology(CXZZBS2017128)
Yuhong LI, Lianli JIAO, Mingyuan HAO, et al. DNA methylation microarray-based screening of epigenetically masked genes in patients with anti-tuberculosis drug-induced liver injury[J]. Journal of Third Military Medical University, 2019, 41(4): 353-359.
DOI:
Yuhong LI, Lianli JIAO, Mingyuan HAO, et al. DNA methylation microarray-based screening of epigenetically masked genes in patients with anti-tuberculosis drug-induced liver injury[J]. Journal of Third Military Medical University, 2019, 41(4): 353-359. DOI: 10.16016/j.1000-5404.201810029.
DNA methylation microarray-based screening of epigenetically masked genes in patients with anti-tuberculosis drug-induced liver injury
摘要
目的
2
采用基因甲基化芯片技术筛选抗结核药物性肝损伤(anti-tuberculosis drug induced liver injury,ADLI)患者与非肝损伤患者间DNA差异甲基化基因位点。探讨DNA甲基化与ADLI发病机制的关系。
To investigate the differentially methylated genes between patients with anti-tuberculosis drug induced liver injury (ADLI) and patients without hepatic injury using DNA methylation microarrays and explore the relationship between DNA methylation and ADLI.
Methods
2
This study was conducted among 137 patients with newly diagnosed pulmonary tuberculosis (including 65 patients with ADLI and 72 without ADLI) treated in the Fourth Hospital of Tangshan City between January
2016 and July
2017. The clinical data were collected and whole blood samples were obtained from all the patients
and 14 patients
including 7 with ADLI and 7 without ADLI
were selected for examination of DNA methylation status using Illumina 850K bead-chip. The methylation status of the 2 differentially methylated genes
DUSP22 and HLA-C
which were identified by analysis of the microarray data
were verified in the remaining cases using methylation-specific PCR (MSP); RT-PCR was used to detect the mRNA levels of DUSP22 and HLA-C genes in all the patients.
Results
2
We analyzed a total of 853 307 loci and identified 1 012 differential methylated loci between ADLI group and non-ADLI group
including 254 hypermethylated and 758 hypomethylated loci
located mainly in the gene body regions. Cluster analysis showed that a large number of differentially methylated genes were involved in the process of cell adhesion and metal ion binding. MSP verified that the methylation rates of DUSP22 and HLA-C genes differed significantly between ADLI group and non-ADLI group (65.6%
vs
36.9%; 37.9%
vs
58.5%; both
P
<
0.05). The mRNA expression of DUSP22 was higher and that of HLA-C was lower in non-ADLI group than in ADLI group.
Conclusion
2
DNA methylation of DUSP22 and HLA-C in the peripheral blood is associated with the development of ADLI.
关键词
Keywords
references
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