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微小RNA及其非病毒载体在椎间盘退变中的研究进展

[Research progress of microRNA and its non-viral vector in intervertebral disc degeneration].

作者信息

Huang Yong, Feng Ganjun, Liu Limin, Li Tao, Liu Hao, Song Yueming

机构信息

Department of Orthopaedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R.China.

Department of Orthopaedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041,

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Jan 1;31(1):116-121. doi: 10.7507/1002-1892.201609092.

DOI:10.7507/1002-1892.201609092
PMID:29798640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9548034/
Abstract

OBJECTIVE

To summarize the research progress of microRNA (miRNA) and its non-viral vector in intervertebral disc degeneration (IDD) and to investigate the potential of non-viral vector delivery of miRNA in clinical application.

METHODS

The related literature about the role of miRNA in IDD and its non-viral delivery system was reviewed and analyzed.

RESULTS

MiRNA can regulate the related gene expression level and further participate in the pathophysiologic process in degenerated intervertebral disc, miRNA delivered by various non-viral vectors has obtained an ideal effect in some diseases.

CONCLUSION

MiRNA plays a great role in the cellular and molecular mechanisms of IDD, as a safe and effective strategy for gene therapy, non-viral vector provides new possibilities for IDD treated with miRNA.

摘要

目的

总结微小RNA(miRNA)及其非病毒载体在椎间盘退变(IDD)中的研究进展,并探讨miRNA非病毒载体递送在临床应用中的潜力。

方法

回顾并分析了有关miRNA在IDD中的作用及其非病毒递送系统的相关文献。

结果

miRNA可调节相关基因表达水平,进而参与退变椎间盘的病理生理过程,多种非病毒载体递送的miRNA在一些疾病中已取得理想效果。

结论

miRNA在IDD的细胞和分子机制中发挥着重要作用,作为一种安全有效的基因治疗策略,非病毒载体为miRNA治疗IDD提供了新的可能性。

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本文引用的文献

1
miR-155 Inhibits Nucleus Pulposus Cells' Degeneration through Targeting ERK 1/2.微小RNA-155通过靶向细胞外信号调节激酶1/2抑制髓核细胞退变。
Dis Markers. 2016;2016:6984270. doi: 10.1155/2016/6984270. Epub 2016 Aug 18.
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MicroRNA-7 regulates IL-1β-induced extracellular matrix degeneration by targeting GDF5 in human nucleus pulposus cells.微小RNA-7通过靶向人髓核细胞中的生长分化因子5来调节白细胞介素-1β诱导的细胞外基质退变。
Biomed Pharmacother. 2016 Oct;83:1414-1421. doi: 10.1016/j.biopha.2016.08.062. Epub 2016 Aug 30.
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Inhibition of microRNA-34a prevents IL-1β-induced extracellular matrix degradation in nucleus pulposus by increasing GDF5 expression.抑制微小RNA-34a可通过增加生长分化因子5(GDF5)的表达来防止白细胞介素-1β(IL-1β)诱导的髓核细胞外基质降解。
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Regulation of insulin-like growth factor 1 receptor signaling by microRNA-4458 in the development of lumbar disc degeneration.微小RNA-4458在腰椎间盘退变发展过程中对胰岛素样生长因子1受体信号通路的调控
Am J Transl Res. 2016 May 15;8(5):2309-16. eCollection 2016.
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Role of microRNA-210 in human intervertebral disc degeneration.微小RNA-210在人类椎间盘退变中的作用
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Matrix stiffness promotes cartilage endplate chondrocyte calcification in disc degeneration via miR-20a targeting ANKH expression.基质硬度通过 miR-20a 靶向 ANKH 表达促进椎间盘退变中软骨终板软骨细胞钙化。
Sci Rep. 2016 May 4;6:25401. doi: 10.1038/srep25401.
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MicroRNA therapeutics: Discovering novel targets and developing specific therapy.微小RNA疗法:发现新靶点并开发特异性治疗方法。
Perspect Clin Res. 2016 Apr-Jun;7(2):68-74. doi: 10.4103/2229-3485.179431.
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Regulation of angiogenesis through the efficient delivery of microRNAs into endothelial cells using polyamine-coated carbon nanotubes.通过使用聚胺涂层碳纳米管将微小RNA高效递送至内皮细胞来调控血管生成。
Nanomedicine. 2016 Aug;12(6):1511-22. doi: 10.1016/j.nano.2016.02.017. Epub 2016 Mar 22.
9
MiR-125a Rs12976445 Polymorphism is Associated with the Apoptosis Status of Nucleus Pulposus Cells and the Risk of Intervertebral Disc Degeneration.MiR-125a Rs12976445多态性与髓核细胞凋亡状态及椎间盘退变风险相关。
Cell Physiol Biochem. 2016;38(1):295-305. doi: 10.1159/000438630. Epub 2016 Jan 25.
10
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.