Novel free-circulating and extracellular vesicle-derived miRNAs dysregulated in Duchenne muscular dystrophy

被引:6
作者
Catapano, Francesco [1 ]
Scaglioni, Dominic [1 ]
Maresh, Kate [1 ]
Ala, Pierpaolo [1 ]
Domingos, Joana [1 ]
Selby, Victoria [1 ]
Ricotti, Valeria [2 ]
Phillips, Lauren [3 ]
Servais, Laurent [4 ,5 ]
Seferian, Andreea [4 ]
de Groot, Imelda [6 ]
Krom, Yvonne D. [7 ,8 ]
Voit, Thomas [2 ]
Verschuuren, J. J. G. M. [7 ,8 ]
Niks, E. H. [7 ,8 ]
Straub, Volker [9 ]
Morgan, Jennifer [1 ,2 ]
Muntoni, Francesco [1 ,2 ]
机构
[1] UCL Great Ormond St Inst Child Hlth, Dubowitz Neuromuscular Ctr, 30 Guildford St, London WC1N 1EH, England
[2] UCL, Natl Inst Hlth Res, Great Ormond St Inst Child Hlth, Biomed Res Ctr, London WC1N 1EH, England
[3] Newcastle Univ, John Walton Muscular Dystrophy Res Ctr, MRC Ctr Neuromuscular Dis, Inst Genet Med, Newcastle Upon Tyne, Tyne & Wear, England
[4] Hop Armand Trousseau, Inst I Mot, Paris, France
[5] CHU Liege, Ctr Reference Malad Neuromusculaires, Liege, Belgium
[6] Radboud Univ Nijmegen, Amalia Childrens Hosp, Dept Rehabil, Med Ctr, Nijmegen, Netherlands
[7] Leiden Univ, Dept Neurol, Med Ctr, Leiden, Netherlands
[8] Duchenne Ctr Netherlands, Leiden, Netherlands
[9] Newcastle Upon Tyne Hosp NHS Fdn Trust, Int Ctr Life, Inst Human Genet, Northern Genet Serv, Cent Pkwy, Newcastle Upon Tyne, Tyne & Wear, England
关键词
biomarkers; corticosteroids; Duchenne muscular dystrophy; extracellular vesicles; microRNAs; plasma; DISEASE PROGRESSION; CREATINE-KINASE; DOWN-REGULATION; SKELETAL; MICRORNAS; EXPRESSION; BIOMARKERS; FIBROSIS; IDENTIFICATION; PROLIFERATION;
D O I
10.2217/epi-2020-0052
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Aim: To perform cross-sectional and longitudinal miRNA profiling in plasma from Duchenne muscular dystrophy (DMD) subjects and find non-invasive biomarkers in DMD. Subjects/materials & methods: Plasma was collected from 14 age and sex matched controls and 46 DMD subjects. Free-circulating and extracellular vesicle (EV)-derived miRNA expression was measured by RT-qPCR. Results: Free-circulating and EVs derived miR-29c-3p and miR-133a-3p are dysregulated in DMD subjects. Free-circulating and EV-derived miR-29c-3p are reduced in DMD subjects undergoing daily corticosteroid treatment. Free-circulating miR-1-3p and miR-122-5p are longitudinally upregulated in ambulant DMD subjects. Conclusion: We detected novel free-circulating and EV-derived dysregulated miRNAs in plasma from DMD subjects and characterized the longitudinal profile of free-circulating miRNA on plasma from DMD subjects.
引用
收藏
页码:1899 / 1915
页数:17
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