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

被引:24
作者
Wang, Wenjun [1 ,2 ]
Shi, Qiang [2 ]
Mattes, Williams B. [2 ]
Mendrick, Donna L. [2 ]
Yang, Xi [2 ]
机构
[1] South Cent Univ Nationalities, Coll Life Sci, Wuhan 430074, Peoples R China
[2] US FDA, Natl Ctr Toxicol Res, Div Syst Biol, Jefferson, AR 72079 USA
关键词
biomarkers; cardiotoxicity; extracellular; hepatotoxicity; microRNA; nephrotoxicity; DROPLET-DIGITAL PCR; CIRCULATING MICRORNAS; MYOCARDIAL DAMAGE; TUBULAR INJURY; PLASMA MIR-208; SMALL RNAS; IDENTIFICATION; EXPRESSION; SERUM; MARKERS;
D O I
10.2217/bmm.15.86
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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.
引用
收藏
页码:1177 / 1188
页数:12
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