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本文引用的文献

1
Transcriptomic differential lncRNA expression is involved in neuropathic pain in rat dorsal root ganglion after spared sciatic nerve injury.转录组学差异lncRNA表达与坐骨神经 spared 损伤后大鼠背根神经节中的神经性疼痛有关。
Braz J Med Biol Res. 2018 Jul 26;51(10):e7113. doi: 10.1590/1414-431X20187113.
2
Noncoding RNAs in disease.非编码 RNA 与疾病
FEBS Lett. 2018 Sep;592(17):2884-2900. doi: 10.1002/1873-3468.13182. Epub 2018 Jul 20.
3
A Network of Noncoding Regulatory RNAs Acts in the Mammalian Brain.非编码调控 RNA 网络在哺乳动物大脑中的作用。
Cell. 2018 Jul 12;174(2):350-362.e17. doi: 10.1016/j.cell.2018.05.022. Epub 2018 Jun 7.
4
LncRNA uc.48+ is involved in the diabetic immune and inflammatory responses mediated by P2X7 receptor in RAW264.7 macrophages.长链非编码 RNA uc.48+ 通过嘌呤能受体 P2X7 介导的 RAW264.7 巨噬细胞的糖尿病免疫和炎症反应。
Int J Mol Med. 2018 Aug;42(2):1152-1160. doi: 10.3892/ijmm.2018.3661. Epub 2018 May 9.
5
Comparative transcriptome profiling of the human and mouse dorsal root ganglia: an RNA-seq-based resource for pain and sensory neuroscience research.人类和小鼠背根神经节的比较转录组分析:基于 RNA-seq 的疼痛和感觉神经科学研究资源。
Pain. 2018 Jul;159(7):1325-1345. doi: 10.1097/j.pain.0000000000001217.
6
Long non‑coding RNA BC168687 small interfering RNA reduces high glucose and high free fatty acid‑induced expression of P2X7 receptors in satellite glial cells.长链非编码 RNA BC168687 小干扰 RNA 降低高糖和高游离脂肪酸诱导的卫星胶质细胞 P2X7 受体表达。
Mol Med Rep. 2018 Apr;17(4):5851-5859. doi: 10.3892/mmr.2018.8601. Epub 2018 Feb 13.
7
Long Non-coding RNA BC168687 is Involved in TRPV1-mediated Diabetic Neuropathic Pain in Rats.长链非编码 RNA BC168687 参与 TRPV1 介导的大鼠糖尿病神经病理性疼痛。
Neuroscience. 2018 Mar 15;374:214-222. doi: 10.1016/j.neuroscience.2018.01.049. Epub 2018 Feb 5.
8
Effects of LncRNA BC168687 siRNA on Diabetic Neuropathic Pain Mediated by P2X Receptor on SGCs in DRG of Rats.长链非编码 RNA BC168687siRNA 对大鼠背根神经节感觉神经元 P2X 受体介导的糖尿病神经病理性疼痛的影响。
Biomed Res Int. 2017;2017:7831251. doi: 10.1155/2017/7831251. Epub 2017 Oct 24.
9
Long non-coding RNA CCAT1 modulates neuropathic pain progression through sponging miR-155.长链非编码RNA CCAT1通过吸附miR-155调节神经性疼痛进展。
Oncotarget. 2017 Sep 23;8(52):89949-89957. doi: 10.18632/oncotarget.21192. eCollection 2017 Oct 27.
10
LncRNA NONRATT021972 Was Associated with Neuropathic Pain Scoring in Patients with Type 2 Diabetes.长链非编码RNA NONRATT021972与2型糖尿病患者的神经性疼痛评分相关。
Behav Neurol. 2017;2017:2941297. doi: 10.1155/2017/2941297. Epub 2017 Aug 8.

长链非编码 RNA(lncRNA):神经病理性疼痛的靶点。

Long noncoding RNA (lncRNA): a target in neuropathic pain.

机构信息

a Department of Anesthesiology , New Jersey Medical School, Rutgers, The State University of New Jersey , Newark , NJ , USA.

出版信息

Expert Opin Ther Targets. 2019 Jan;23(1):15-20. doi: 10.1080/14728222.2019.1550075. Epub 2018 Dec 2.

DOI:10.1080/14728222.2019.1550075
PMID:30451044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6294120/
Abstract

Current treatments for neuropathic pain are limited in part due to the incomplete understanding of its underlying mechanisms. Recent evidence reveals the dysregulated expression of long non-coding RNAs (lncRNAs) in the damaged nerve, dorsal root ganglion (DRG), and spinal cord dorsal horn following peripheral nerve injury. However, the role of the majority of lncRNAs in neuropathic pain genesis is still elusive. Unveiling the mechanisms of how lncRNAs participate in neuropathic pain may develop new strategies to prevent and/or treat this disorder. Areas covered: This review focuses on the dysregulation of lncRNAs in the DRG, dorsal horn, and the injured nerves from preclinical models of neuropathic pain. We provide evidence of how peripheral nerve injury causes the dysregulation of lncRNAs in these pain-related regions. The potential mechanisms of how dysregulated lncRNAs contribute to the pathogenesis of neuropathic pain are discussed. Expert opinion: The investigation on the role of the dysregulated lncRNAs in neuropathic pain might open up a novel avenue for therapeutic treatment of this disorder. However, current investigation is at the infancy stage, which challenges the translation of preclinical findings. More intensive studies on lncRNAs are required before the preclinical findings are translated into therapeutic management for neuropathic pain.

摘要

目前针对神经病理性疼痛的治疗方法有限,部分原因是对其潜在机制的不完全了解。最近的证据表明,在周围神经损伤后,受损神经、背根神经节 (DRG) 和脊髓背角中长链非编码 RNA (lncRNA) 的表达失调。然而,大多数 lncRNA 在神经病理性疼痛发生中的作用仍然难以捉摸。揭示 lncRNA 参与神经病理性疼痛的机制可能为预防和/或治疗这种疾病开发新策略。涵盖领域:本综述重点关注神经病理性疼痛的临床前模型中 DRG、背角和损伤神经中 lncRNA 的失调。我们提供了证据表明外周神经损伤如何导致这些与疼痛相关区域中 lncRNA 的失调。讨论了失调 lncRNA 如何有助于神经病理性疼痛发病机制的潜在机制。专家意见:对失调 lncRNA 在神经病理性疼痛中的作用的研究可能为这种疾病的治疗开辟新途径。然而,目前的研究处于起步阶段,这对临床前发现的转化提出了挑战。在将临床前发现转化为神经病理性疼痛的治疗管理之前,需要对 lncRNA 进行更多的研究。