Identification of tubular injury microRNA biomarkers in urine: comparison of next-generation sequencing and qPCR-based profiling platforms

被引:69
作者
Nassirpour, Rounak [1 ]
Mathur, Sachin [2 ]
Gosink, Mark M. [3 ]
Li, Yizheng [2 ]
Shoieb, Ahmed M. [3 ]
Wood, Joanna [4 ]
O'Neil, Shawn P. [1 ]
Homer, Bruce L. [1 ]
Whiteley, Laurence O. [1 ]
机构
[1] Pfizer Worldwide Res & Dev, Drug Safety, Andover, MA 01810 USA
[2] Pfizer Res & Dev, Business Technol, Andover, MA 01810 USA
[3] Pfizer Res & Dev, Drug Safety, Andover, MA 01810 USA
[4] Guys Hosp, Quintiles Drug Res Unit, London SE1 1YR, England
关键词
Next-generation sequencing; NGS; Small RNA; TruSeq; qRT-PCR; Urine; miRNA; Gentamicin; Kidney injury; DIFFERENTIAL EXPRESSION ANALYSIS; ACUTE KIDNEY INJURY; RAT MODEL; GENTAMICIN; NEPHROTOXICITY; MIRNA; MICROARRAY;
D O I
10.1186/1471-2164-15-485
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: MicroRNAs (miRNAs) are small, non-coding RNAs that regulate protein levels post-transcriptionally. miRNAs play important regulatory roles in many cellular processes and have been implicated in several diseases. Recent studies have reported significant levels of miRNAs in a variety of body fluids, raising the possibility that miRNAs could serve as useful biomarkers. Next-generation sequencing (NGS) is increasingly employed in biomedical investigations. Although concordance between this platform and qRT-PCR based assays has been reported in high quality specimens, information is lacking on comparisons in biofluids especially urine. Here we describe the changes in miRNA expression patterns in a rodent model of renal tubular injury (gentamicin). Our aim is to compare RNA sequencing and qPCR based miRNA profiling in urine specimen from control and rats with confirmed tubular injury. Results: Our preliminary examination of the concordance between miRNA-seq and qRT-PCR in urine specimen suggests minimal agreement between platforms probably due to the differences in sensitivity. Our results suggest that although miRNA-seq has superior specificity, it may not detect low abundant miRNAs in urine samples. Specifically, miRNA-seq did not detect some sequences which were identified by qRT-PCR. On the other hand, the qRT-PCR analysis was not able to detect the miRNA isoforms, which made up the majority of miRNA changes detected by NGS. Conclusions: To our knowledge, this is the first time that miRNA profiling platforms including NGS have been compared in urine specimen. miRNAs identified by both platforms, let-7d, miR-203, and miR-320, may potentially serve as promising novel urinary biomarkers for drug induced renal tubular epithelial injury.
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页数:15
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