A urinary extracellular vesicle microRNA biomarker discovery pipeline; from automated extracellular vesicle enrichment by acoustic trapping to microRNA sequencing

被引:25
作者
Ku, Anson [1 ,9 ]
Ravi, Naveen [2 ]
Yang, Minjun [2 ]
Evander, Mikael [3 ]
Laurell, Thomas [3 ]
Lilja, Hans [1 ,4 ,5 ,6 ,7 ]
Ceder, Yvonne [8 ]
机构
[1] Lund Univ, Dept Translat Med, Malmo, Sweden
[2] Lund Univ, Dept Lab Med, Div Clin Genet, Lund, Sweden
[3] Lund Univ, Dept Biomed Engn, Lund, Sweden
[4] Mem Sloan Kettering Canc Ctr, Dept Surg, Urol Serv, New York, NY 10021 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med, Genitourinary Oncol Serv, 1275 York Ave, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Lab Med, 1275 York Ave, New York, NY 10021 USA
[7] Univ Oxford, Nuffield Dept Surg Sci, Oxford, England
[8] Lund Univ, Div Translat Canc Res, Dept Lab Med, Lund, Sweden
[9] Lund Univ, Dept Lab Med, Lund, Sweden
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
BIASES; IDENTIFICATION;
D O I
10.1371/journal.pone.0217507
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development of a robust automated platform for enrichment of extracellular vesicles from low sample volume that matches the needs for next-generation sequencing could remove major hurdles for genomic biomarker discovery. Here, we document a protocol for urinary EVs enrichment by utilizing an automated microfluidic system, termed acoustic trap, followed by next-generation sequencing of microRNAs (miRNAs) for biomarker discovery. Specifically, we compared the sequencing output from two small RNA library preparations, NEXTFlex and CATS, using only 130 pg of input total RNA. The samples prepared using NEXTflex was found to contain larger number of unique miRNAs that was the predominant RNA species whereas rRNA was the dominant RNA species in CATS prepared samples. A strong correlation was found between the miRNA expressions of the acoustic trap technical replicate in the NEXTFlex prepared samples, as well as between the acoustic trap and ultracentrifugation enrichment methods. Together, these results demonstrate a robust and automated strategy for biomarker discovery from small volumes of urine.
引用
收藏
页数:13
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