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[微小RNA:一种用于椎间盘退变的新型调节因子]

[MicroRNAs: a type of novel regulative factor for intervertebral disc degeneration].

作者信息

Wang Cheng, Wang Wenjun, Yang Wei, Yu Xiaohua, Yan Yiguo, Zhang Jian, Jiang Zhisheng

机构信息

Institute of Cardiovascular Disease, Key Laboratory for Arteriosclerology of Hunan Province, University of South China, Hengyang 421001, China; Department of Spine Surgery, the First Affiliated Hospital, University of South China, Hengyang 421001, China.

Department of Spine Surgery, the First Affiliated Hospital, University of South China, Hengyang 421001, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2016 Mar;45(2):170-8. doi: 10.3785/j.issn.1008-9292.2016.03.10.

DOI:10.3785/j.issn.1008-9292.2016.03.10
PMID:27273991
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10397014/
Abstract

Intervertebral disc degeneration (IDD) is one of major causes for intervertebral disc degenerative diseases, and patients with IDD usually suffer from serious low back pain. The current treatments for patients with IDD only relieve the clinical symptom rather than restore biological balance of IDD, leading to inadequate and unsatisfactory results. MicroRNAs (miRNAs) are endogenous, non-coding, single-stranded RNA molecules, which regulate the gene expression at the post-transcription levels. Research evidences support the involvement of miRNAs in many biological processes, such as lipid metabolism, apoptosis, differentiation and organ development. Accumulating evidences indicate that the expressions of miRNAs change significantly in degenerative tissues. In addition, dysregulated miRNAs contribute to multiple pathological process of IDD, including proliferation and apoptosis of nucleus pulposus and extracellular matrix components, inflammatory response and cartilage endplates degeneration. In this review article, we summarize the expression profiles and roles of miRNAs in IDD, which may provide a novel strategy of biological therapy for the disease.

摘要

椎间盘退变(IDD)是椎间盘退行性疾病的主要病因之一,IDD患者通常遭受严重的腰痛。目前针对IDD患者的治疗仅能缓解临床症状,而非恢复IDD的生物平衡,导致治疗效果不足且不尽人意。微小RNA(miRNA)是内源性、非编码的单链RNA分子,其在转录后水平调节基因表达。研究证据支持miRNA参与许多生物学过程,如脂质代谢、细胞凋亡、分化和器官发育。越来越多的证据表明,miRNA在退变组织中的表达发生显著变化。此外,失调的miRNA促成了IDD的多个病理过程,包括髓核和细胞外基质成分的增殖与凋亡、炎症反应以及软骨终板退变。在这篇综述文章中,我们总结了miRNA在IDD中的表达谱和作用,这可能为该疾病提供一种新的生物治疗策略。

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引用本文的文献

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Long Non-Coding RNAs H19 and HOTAIR Implicated in Intervertebral Disc Degeneration.长链非编码RNA H19和HOTAIR与椎间盘退变有关。
Front Genet. 2022 Mar 3;13:843599. doi: 10.3389/fgene.2022.843599. eCollection 2022.
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Exosome-Transported circRNA_0000253 Competitively Adsorbs MicroRNA-141-5p and Increases IDD.外泌体转运的环状RNA_0000253竞争性吸附微小RNA-141-5p并加重椎间盘退变。
Mol Ther Nucleic Acids. 2020 Sep 4;21:1087-1099. doi: 10.1016/j.omtn.2020.07.039. Epub 2020 Jul 31.

本文引用的文献

1
Dysregulated miR-133a Mediates Loss of Type II Collagen by Directly Targeting Matrix Metalloproteinase 9 (MMP9) in Human Intervertebral Disc Degeneration.失调的miR-133a通过直接靶向人类椎间盘退变中的基质金属蛋白酶9(MMP9)介导II型胶原蛋白的缺失。
Spine (Phila Pa 1976). 2016 Jun;41(12):E717-E724. doi: 10.1097/BRS.0000000000001375.
2
Downregulation of microRNA-193a-3p is involved in invertebral disc degeneration by targeting MMP14.微小RNA-193a-3p的下调通过靶向基质金属蛋白酶14参与椎间盘退变。
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Dysregulated miR-98 Contributes to Extracellular Matrix Degradation by Targeting IL-6/STAT3 Signaling Pathway in Human Intervertebral Disc Degeneration.失调的miR-98通过靶向人椎间盘退变中的IL-6/STAT3信号通路促进细胞外基质降解。
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4
Downregulation of miR-27b is Involved in Loss of Type II Collagen by Directly Targeting Matrix Metalloproteinase 13 (MMP13) in Human Intervertebral Disc Degeneration.在人类椎间盘退变中,miR-27b的下调通过直接靶向基质金属蛋白酶13(MMP13)参与II型胶原蛋白的丢失。
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Interleukin-1β in intervertebral disk degeneration.白细胞介素-1β与椎间盘退变。
Clin Chim Acta. 2015 Oct 23;450:262-72. doi: 10.1016/j.cca.2015.08.029. Epub 2015 Sep 2.
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Autophagy in bone: Self-eating to stay in balance.骨骼中的自噬:自我吞噬以维持平衡。
Ageing Res Rev. 2015 Nov;24(Pt B):206-17. doi: 10.1016/j.arr.2015.08.004. Epub 2015 Aug 28.
7
Lumbar Disc Degeneration is Facilitated by MiR-100-Mediated FGFR3 Suppression.微小RNA-100介导的成纤维细胞生长因子受体3抑制促进腰椎间盘退变
Cell Physiol Biochem. 2015;36(6):2229-36. doi: 10.1159/000430187. Epub 2015 Jul 24.
8
Stem Cell Approaches to Intervertebral Disc Regeneration: Obstacles from the Disc Microenvironment.椎间盘再生的干细胞疗法:来自椎间盘微环境的障碍
Stem Cells Dev. 2015 Nov 1;24(21):2479-95. doi: 10.1089/scd.2015.0158. Epub 2015 Sep 3.
9
MiR-20a-5p mediates hypoxia-induced autophagy by targeting ATG16L1 in ischemic kidney injury.miR-20a-5p 通过靶向 ATG16L1 介导缺氧诱导的自噬在缺血性肾损伤中。
Life Sci. 2015 Sep 1;136:133-41. doi: 10.1016/j.lfs.2015.07.002. Epub 2015 Jul 10.
10
Autophagy attenuates the catabolic effect during inflammatory conditions in nucleus pulposus cells, as sustained by NF-κB and JNK inhibition.自噬减弱了髓核细胞在炎症状态下的分解代谢作用,这一作用由NF-κB和JNK抑制所维持。
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