MicroRNA Biomarkers of Toxicity in Biological Matrices

被引:53
作者
Harrill, Alison H. [1 ]
McCullough, Shaun D. [2 ]
Wood, Charles E. [2 ]
Kahle, Juliette J. [2 ,3 ]
Chorley, Brian N. [1 ]
机构
[1] Univ Arkansas Med Sci, Dept Environm & Occupat Hlth, Little Rock, AR 72205 USA
[2] US EPA, ORD, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27709 USA
[3] Counsyl Inc, 180 Kimball Way, San Francisco, CA 94080 USA
关键词
microRNA; biomarkers; liquid biopsy; tissue injury and toxicity; accessible matrices; ACUTE MYOCARDIAL-INFARCTION; INDUCED LIVER-INJURY; CIRCULATING MICRORNAS; PANCREATIC INJURY; EXTRACELLULAR MICRORNAS; POTENTIAL BIOMARKERS; HEALTHY-VOLUNTEERS; SAFETY ASSESSMENT; PLASMA MICRORNAS; TUBULAR INJURY;
D O I
10.1093/toxsci/kfw090
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Biomarker measurements that reliably correlate with tissue injury and that can be measured within accessible biofluids offer benefits in terms of cost, time, and convenience when assessing chemical and drug-induced toxicity in model systems or human cohorts. MicroRNAs (miRNAs) have emerged in recent years as a promising new class of biomarker for monitoring toxicity. Recent enthusiasm for miRNA biomarker research has been fueled by evidence that certain miRNAs are cell-type specific and are released during injury, thus raising the possibility of using biofluid-based miRNAs as a "liquid biopsy" that may be obtained by sampling extracellular fluids. As biomarkers, miRNAs demonstrate improved stability as compared with many protein markers and sequences are largely conserved across species, simplifying analytical techniques. Recent efforts have sought to identify miRNAs that are released into accessible biofluids following xenobiotic exposure, using compounds that target specific organs. Whereas still early in the discovery phase, miRNA biomarkers will have an increasingly important role in the assessment of adverse effects of both environmental chemicals and pharmaceutical drugs. Here, we review the current findings of biofluid-based miRNAs, as well as highlight technical challenges in assessing toxicologic pathology using these biomarkers.
引用
收藏
页码:264 / 272
页数:9
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