Epigenetic changes in Mycobacterium tuberculosis and its host provide potential targets or biomarkers for drug discovery and clinical diagnosis

被引:12
|
作者
Sui, Jing [1 ,2 ]
Qiao, Wenliang [3 ]
Xiang, Xinrong [1 ,2 ]
Luo, Youfu [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Lung Canc Ctr, Lab Lung Canc, Western China Hosp, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Mycobacterium tuberculosis; Epigenetics; DNA methylation; Histone modification; MicroRNA; METALLOPROTEINASE-1; AND-3; EXPRESSION; RIBOSOMAL-RNA METHYLTRANSFERASE; NF-KAPPA-B; DNA METHYLATION; IMMUNE-RESPONSES; CPG DNA; MATRIX METALLOPROTEINASES; DIRECTED THERAPY; INNATE IMMUNITY; VITAMIN-D;
D O I
10.1016/j.phrs.2022.106195
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tuberculosis infection caused by the contagious pathogen Mycobacterium tuberculosis (MTB) is one of the ancient diseases in the world. The problem of drug resistance is a difficulty in tuberculosis treatment. MTB engendered epigenetic changes play vital parts in escaping the host immune response and bring about the persistence as well as bacterial expansion. This article describes the epigenetic changes that occur in the pathogen MTB and its host during infection, including DNA methylation, histone modification and microRNA, and summarizes their research progress in drug discovery and tuberculosis diagnosis, providing new ideas and strategies to combat against drug-resistant tuberculosis.
引用
收藏
页数:13
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