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Circulating miRNAs are generic and versatile therapeutic monitoring biomarkers in muscular dystrophies

机译:循环miRNA是肌肉营养不良的通用且用途广泛的治疗监测生物标志物

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摘要

The development of medical approaches requires preclinical and clinical trials for assessment of therapeutic efficacy. Such evaluation entails the use of biomarkers, which provide information on the response to the therapeutic intervention. One newly-proposed class of biomarkers is the microRNA (miRNA) molecules. In muscular dystrophies (MD), the dysregulation of miRNAs was initially observed in muscle biopsy and later extended to plasma samples, suggesting that they may be of interest as biomarkers. First, we demonstrated that dystromiRs dysregulation occurs in MD with either preserved or disrupted expression of the dystrophin-associated glycoprotein complex, supporting the utilization of dystromiRs as generic biomarkers in MD. Then, we aimed at evaluation of the capacity of miRNAs as monitoring biomarkers for experimental therapeutic approach in MD. To this end, we took advantage of our previously characterized gene therapy approach in a mouse model for α-sarcoglycanopathy. We identified a dose-response correlation between the expression of miRNAs on both muscle tissue and blood serum and the therapeutic benefit as evaluated by a set of new and classically-used evaluation methods. This study supports the utility of profiling circulating miRNAs for the evaluation of therapeutic outcome in medical approaches for MD.
机译:医学方法的发展需要临床前和临床试验以评估治疗效果。这种评估需要使用生物标志物,该标志物可提供有关对治疗干预措施的反应的信息。一类新提出的生物标志物是microRNA(miRNA)分子。在肌肉营养不良症(MD)中,最初在肌肉活检中观察到miRNA的失调,后来扩展到血浆样品,这表明它们可能作为生物标记物而受到关注。首先,我们证明dystromiRs失调发生在MD中,与dystrophin相关的糖蛋白复合物的表达保持或破坏,支持dystromiRs作为MD中的通用生物标志物的利用。然后,我们旨在评估miRNA作为监测MD实验性治疗方法的生物标志物的能力。为此,我们在α-肌糖蛋白病的小鼠模型中利用了我们先前表征的基因治疗方法。通过一组新的和经典使用的评估方法,我们确定了在肌肉组织和血清中的miRNA表达与治疗效果之间的剂量反应相关性。这项研究支持对循环中的miRNA进行谱分析以评估MD医学方法的治疗效果的实用性。

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