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Translating extracellular microRNA into clinical biomarkers for drug-induced toxicity: from high-throughput profiling to validation

机译:将细胞外microRNA转化为用于药物诱导毒性的临床生物标记物:从高通量分析到验证

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摘要

Over the past 5 years, extracellular microRNAs (miRNAs) are being vigorously explored as injury biomarkers, including drug-induced cardiotoxicity, hepatotoxicity and nephrotoxicity. Currently, the development of miRNAs as clinical biomarkers has been hindered by the lack of standardization. Therefore, extracellular miRNA-based biomarkers have not been embraced as diagnostic tools. Each platform has its strengths and weaknesses when working with low-input-amount RNA samples from body fluids; the selection of a miRNA quantification approach should be based on the study design. The following review provides a summary of the extracellular miRNA release and stability in body fluids, performances of different miRNA quantification platforms, existing clinical gold standards for drug-induced tissue damage and translation of the miRNA biomarkers from the nonclinical to clinical setting.
机译:在过去的5年中,正在积极探索细胞外微RNA(miRNA)作为损伤生物标志物,包括药物诱导的心脏毒性,肝毒性和肾毒性。当前,由于缺乏标准化,已经阻碍了miRNA作为临床生物标记物的开发。因此,基于细胞外miRNA的生物标志物尚未被接受为诊断工具。当处理来自体液的低投入量RNA样品时,每个平台都有其优点和缺点。 miRNA定量方法的选择应基于研究设计。以下综述总结了细胞外miRNA在体液中的释放和稳定性,不同miRNA定量平台的性能,药物诱导的组织损伤的现有临床金标准以及miRNA生物标志物从非临床到临床的转化。

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