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青光眼和神经退行性疾病中的微小RNA

MicroRNAs in glaucoma and neurodegenerative diseases.

作者信息

Molasy Milena, Walczak Anna, Szaflik Jerzy, Szaflik Jacek P, Majsterek Ireneusz

机构信息

Department of Clinical Chemistry and Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.

Department of Ophthalmology, SPKSO Ophthalmic Hospital, Medical University of Warsaw, Warsaw, Poland.

出版信息

J Hum Genet. 2017 Jan;62(1):105-112. doi: 10.1038/jhg.2016.91. Epub 2016 Jul 14.

DOI:10.1038/jhg.2016.91
PMID:27412874
Abstract

MicroRNAs (miRNAs) constitute a class of short, non-coding RNAs, which have important role in post-transcriptional regulation of genes expression by base-pairing with their target messenger RNA (mRNA). In recent years, miRNAs biogenesis, gene silencing mechanism and implication in various diseases have been thoroughly investigated. Many scientific findings indicate the altered expression of specific miRNA in the brains of patients affected by neurodegenerative diseases (NDs) such as Alzheimer's disease, Parkinson's disease and Huntington disease. The progressive optic nerve neuropathy associated with changed miRNA profile was also observed during glaucoma development. This suggests that the miRNAs may have a crucial role in these disorders, contributing to the neuronal cell death. A better understanding of molecular mechanism of these disorders will open a new potential way of ND treatment. In this review, the miRNAs role in particular neurodegenerative disorders and their possible application in medicine was discussed.

摘要

微小RNA(miRNA)是一类短链非编码RNA,通过与靶信使核糖核酸(mRNA)碱基配对在基因表达的转录后调控中发挥重要作用。近年来,对miRNA的生物合成、基因沉默机制及其在各种疾病中的作用进行了深入研究。许多科学发现表明,在患有神经退行性疾病(NDs)如阿尔茨海默病、帕金森病和亨廷顿病的患者大脑中,特定miRNA的表达发生了改变。在青光眼发展过程中也观察到与miRNA谱改变相关的进行性视神经病变。这表明miRNA可能在这些疾病中起关键作用,导致神经元细胞死亡。更好地理解这些疾病的分子机制将为神经退行性疾病的治疗开辟一条新的潜在途径。在这篇综述中,讨论了miRNA在特定神经退行性疾病中的作用及其在医学中的可能应用。

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1
Expression profiling of microRNAs in optineurin (E50K) mutant transgenic mice.视紫质(E50K)突变转基因小鼠中微小RNA的表达谱分析。
Biomed Rep. 2016 Feb;4(2):193-196. doi: 10.3892/br.2015.565. Epub 2015 Dec 31.
2
MicroRNA Expression in the Glaucomatous Retina.青光眼视网膜中的微小RNA表达
Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7971-82. doi: 10.1167/iovs.15-18088.
3
Molecular Damage in Glaucoma: from Anterior to Posterior Eye Segment. The MicroRNA Role.青光眼的分子损伤:从眼前节到眼后节。微小RNA的作用。
缺血诱导的视网膜星形胶质细胞来源的外泌体在缺血性视网膜病变中导致视网膜神经节细胞凋亡的新功能及机制
Mol Ther Nucleic Acids. 2024 May 7;35(2):102209. doi: 10.1016/j.omtn.2024.102209. eCollection 2024 Jun 11.
4
miR-101a-3p/ROCK2 axis regulates neuronal injury in Parkinson's disease models.miR-101a-3p/ROCK2 轴调节帕金森病模型中的神经元损伤。
Aging (Albany NY). 2024 May 21;16(10):8732-8746. doi: 10.18632/aging.205836.
5
Exploring Epigenetic Modifications as Potential Biomarkers and Therapeutic Targets in Glaucoma.探索表观遗传修饰作为青光眼潜在的生物标志物和治疗靶点
Int J Mol Sci. 2024 Feb 29;25(5):2822. doi: 10.3390/ijms25052822.
6
Expression of microRNAs related to apoptosis in the aqueous humor and lens capsule of patients with glaucoma.青光眼患者房水和晶状体囊膜中与细胞凋亡相关的微小RNA的表达
Front Med (Lausanne). 2024 Feb 14;11:1288854. doi: 10.3389/fmed.2024.1288854. eCollection 2024.
7
A Comprehensive Bioinformatics Approach to Identify Molecular Signatures and Key Pathways for the Huntington Disease.一种用于识别亨廷顿病分子特征和关键通路的综合生物信息学方法。
Bioinform Biol Insights. 2023 Nov 27;17:11779322231210098. doi: 10.1177/11779322231210098. eCollection 2023.
8
The Application of MicroRNAs in Glaucoma Research: A Bibliometric and Visualized Analysis.微小 RNA 在青光眼研究中的应用:文献计量学和可视化分析。
Int J Mol Sci. 2023 Oct 19;24(20):15377. doi: 10.3390/ijms242015377.
9
miRNA Studies in Glaucoma: A Comprehensive Review of Current Knowledge and Future Perspectives.miRNA 在青光眼研究中的作用:当前知识与未来展望的综合综述。
Int J Mol Sci. 2023 Sep 28;24(19):14699. doi: 10.3390/ijms241914699.
10
Exploring Early-Stage Retinal Neurodegeneration in Murine Pigmentary Glaucoma: Insights From Gene Networks and miRNA Regulation Analyses.探索小鼠色素性青光眼的早期视网膜神经退行性变:基因网络和 miRNA 调控分析的见解。
Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):25. doi: 10.1167/iovs.64.12.25.
Microrna. 2015;4(1):3-17. doi: 10.2174/2211536604666150707124640.
4
Are RNAi and miRNA therapeutics truly dead?RNAi 和 miRNA 疗法真的死了吗?
Trends Biotechnol. 2015 Mar;33(3):141-4. doi: 10.1016/j.tibtech.2014.12.005. Epub 2015 Jan 13.
5
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BMC Mol Biol. 2014 Nov 18;15:25. doi: 10.1186/s12867-014-0025-1.
6
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7
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Sci Rep. 2014 May 28;4:5089. doi: 10.1038/srep05089.
8
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JAMA. 2014 May 14;311(18):1901-11. doi: 10.1001/jama.2014.3192.
9
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Int J Genomics. 2014;2014:165897. doi: 10.1155/2014/165897. Epub 2014 Mar 5.
10
The involvement of microRNAs in neurodegenerative diseases.微小 RNA 与神经退行性疾病的关系。
Front Cell Neurosci. 2013 Dec 19;7:265. doi: 10.3389/fncel.2013.00265.