Noncoding RNAs and Duchenne muscular dystrophy

被引:18
作者
Perry, Mark M. [1 ]
Muntoni, Francesco [1 ]
机构
[1] UCL Inst Child Hlth, Dubowitz Neuromuscular Ctr, Mol Neurosci Sect, Dev Neurosci Programme, 30 Guildford St, London WC1N 1EH, England
关键词
Duchenne muscular dystrophy; GRMD dog; lncRNA; MDX mice; miRNA; MUSCLE DIFFERENTIATION; DISTINCTIVE PATTERNS; MICRORNA EXPRESSION; SERUM BIOMARKERS; MIR-206; MIRNAS; PROGRESSION; BIOGENESIS; MECHANISM; MIR-133A;
D O I
10.2217/epi-2016-0088
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Noncoding RNAs (ncRNAs) such as miRNAs and long noncoding RNAs modulate gene transcription in response to environmental stressors and other stimuli. A role for ncRNAs in muscle pathologies has been demonstrated and further evidence suggests that ncRNAs also play a role in Duchenne muscular dystrophy (DMD). Studies investigating the differential expression of miRNAs in biological fluids between DMD patients and models of dystrophin deficiency (the MDX mouse model, canine models of DMD) and controls have been published, as these have a role in fibrosis. Long noncoding RNAs are differentially expressed in DMD patients and may, in part, have a mechanism of action via targeting of miRNAs. Although many of these recent findings need to be confirmed, ncRNAs may prove to be useful as potential biomarkers of disease. However, their use as therapeutic targets in DMD remains unclear.
引用
收藏
页码:1527 / 1537
页数:11
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