TY - JOUR
T1 - Plasma extracellular RNA profiles in healthy and cancer patients
AU - Yuan, Tiezheng
AU - Huang, Xiaoyi
AU - Woodcock, Mark
AU - Du, Meijun
AU - Dittmar, Rachel
AU - Wang, Yuan
AU - Tsai, Susan
AU - Kohli, Manish
AU - Boardman, Lisa
AU - Patel, Tushar
AU - Wang, Liang
N1 - Funding Information:
We thank Sequencing Core at the Medical College of Wisconsin for sequencing consultation and support. This work was supported by Advancing a Healthier Wisconsin fund (project#5520227) to LW and National Institute of Health (3UH2TR000884) to TP.
PY - 2016/1/20
Y1 - 2016/1/20
N2 - Extracellular vesicles are selectively enriched in RNA that has potential as disease biomarkers. To systemically characterize circulating extracellular RNA (exRNA) profiles, we performed RNA sequencing analysis on plasma extracellular vesicles derived from 50 healthy individuals and 142 cancer patients. Of ∼12.6 million raw reads for each individual, the number of mappable reads aligned to RNA references was ∼5.4 million including miRNAs (∼40.4%), piwiRNAs (∼40.0%), pseudo-genes (∼3.7%), lncRNAs (∼2.4%), tRNAs (∼2.1%), and mRNAs (∼2.1%). By expression stability testing, we identified a set of miRNAs showing relatively consistent expression, which may serve as reference control for exRNA quantification. By performing multivariate analysis of covariance, we identified significant associations of these exRNAs with age, sex and different types of cancers. In particular, down-regulation of miR-125a-5p and miR-1343-3p showed an association with all cancer types tested (false discovery rate <0.05). We developed multivariate statistical models to predict cancer status with an area under the curve from 0.68 to 0.92 depending cancer type and staging. This is the largest RNA-seq study to date for profiling exRNA species, which has not only provided a baseline reference profile for circulating exRNA, but also revealed a set of RNA candidates for reference controls and disease biomarkers.
AB - Extracellular vesicles are selectively enriched in RNA that has potential as disease biomarkers. To systemically characterize circulating extracellular RNA (exRNA) profiles, we performed RNA sequencing analysis on plasma extracellular vesicles derived from 50 healthy individuals and 142 cancer patients. Of ∼12.6 million raw reads for each individual, the number of mappable reads aligned to RNA references was ∼5.4 million including miRNAs (∼40.4%), piwiRNAs (∼40.0%), pseudo-genes (∼3.7%), lncRNAs (∼2.4%), tRNAs (∼2.1%), and mRNAs (∼2.1%). By expression stability testing, we identified a set of miRNAs showing relatively consistent expression, which may serve as reference control for exRNA quantification. By performing multivariate analysis of covariance, we identified significant associations of these exRNAs with age, sex and different types of cancers. In particular, down-regulation of miR-125a-5p and miR-1343-3p showed an association with all cancer types tested (false discovery rate <0.05). We developed multivariate statistical models to predict cancer status with an area under the curve from 0.68 to 0.92 depending cancer type and staging. This is the largest RNA-seq study to date for profiling exRNA species, which has not only provided a baseline reference profile for circulating exRNA, but also revealed a set of RNA candidates for reference controls and disease biomarkers.
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U2 - 10.1038/srep19413
DO - 10.1038/srep19413
M3 - Article
C2 - 26786760
AN - SCOPUS:84955275191
SN - 2045-2322
VL - 6
JO - Scientific reports
JF - Scientific reports
M1 - 19413
ER -