DNA Methylation: A Target in Neuropathic Pain

被引:10
作者
Jiang, Wei [1 ,2 ]
Tan, Xuan-Yu [3 ]
Li, Jia-Ming [4 ]
Yu, Peng [5 ]
Dong, Ming [1 ,2 ]
机构
[1] First Hosp Jilin Univ, Dept Neurol, Changchun, Peoples R China
[2] First Hosp Jilin Univ, Neurosci Ctr, Changchun, Peoples R China
[3] First Hosp Jilin Univ, Dept Neurosurg, Changchun, Peoples R China
[4] First Hosp Jilin Univ, Dept Emergency, Changchun, Peoples R China
[5] Second Hosp Jilin Univ, Dept Ophthalmol, Changchun, Peoples R China
基金
中国国家自然科学基金;
关键词
neuropathic pain; DNA methylation; gene suppression; epigenetic; treatment; DORSAL-ROOT GANGLION; CPG-BINDING PROTEIN-2; MAMMALIAN DNA; METHYLTRANSFERASE INHIBITORS; OPIOID RECEPTOR; DOWN-REGULATION; SEX-DIFFERENCES; TET PROTEINS; EXPRESSION; EPIGENETICS;
D O I
10.3389/fmed.2022.879902
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neuropathic pain (NP), caused by an injury or a disease affecting the somatosensory nervous system of the central and peripheral nervous systems, has become a global health concern. Recent studies have demonstrated that epigenetic mechanisms are among those that underlie NP; thus, elucidating the molecular mechanism of DNA methylation is crucial to discovering new therapeutic methods for NP. In this review, we first briefly discuss DNA methylation, demethylation, and the associated key enzymes, such as methylases and demethylases. We then discuss the relationship between NP and DNA methylation, focusing on DNA methyltransferases including methyl-CpG-binding domain (MBD) family proteins and ten-eleven translocation (TET) enzymes. Based on experimental results of neuralgia in animal models, the mechanism of DNA methylation-related neuralgia is summarized, and useful targets for early drug intervention in NP are discussed.
引用
收藏
页数:10
相关论文
共 103 条
[1]   TET enzymes in neurophysiology and brain function [J].
Antunes, Claudia ;
Sousa, Nuno ;
Pinto, Luisa ;
Joana Marques, C. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2019, 102 :337-344
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Sex differences in pain: a brief review of clinical and experimental findings [J].
Bartley, E. J. ;
Fillingim, R. B. .
BRITISH JOURNAL OF ANAESTHESIA, 2013, 111 (01) :52-58
[4]   MBD5 and MBD6 interact with the human PR-DUB complex through their methyl-CpG-binding domain [J].
Baymaz, H. Irem ;
Fournier, Alexandra ;
Laget, Sophie ;
Ji, Zongling ;
Jansen, Pascal W. T. C. ;
Smits, Arne H. ;
Ferry, Laure ;
Mensinga, Anneloes ;
Poser, Ina ;
Sharrocks, Andrew ;
Defossez, Pierre-Antoine ;
Vermeulen, Michiel .
PROTEOMICS, 2014, 14 (19) :2179-2189
[5]   Predictive validity of behavioural animal models for chronic pain [J].
Berge, Odd-Geir .
BRITISH JOURNAL OF PHARMACOLOGY, 2011, 164 (04) :1195-1206
[6]  
BIRD A, 1985, CELL, V40, P91, DOI 10.1016/0092-8674(85)90312-5
[7]   Lost but making progress-Where will new analgesic drugs come from? [J].
Borsook, David ;
Hargreaves, Richard ;
Bountra, Chas ;
Porreca, Frank .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (249)
[8]   DNA methyltransferase inhibitors: old and new drugs for an epigenetic cancer therapy [J].
Brueckner, B ;
Lyko, F .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2004, 25 (11) :551-554
[9]   DNA methyltransferase inhibitors for cancer therapy [J].
Brueckner, Bodo ;
Kuck, Dirk ;
Lyko, Frank .
CANCER JOURNAL, 2007, 13 (01) :17-22
[10]   Mechanisms of neuropathic pain [J].
Campbell, James N. ;
Meyer, Richard A. .
NEURON, 2006, 52 (01) :77-92