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Plasma extracellular RNA profiles in healthy and cancer patients

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 patie...

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Autores principales: Yuan, Tiezheng, Huang, Xiaoyi, Woodcock, Mark, Du, Meijun, Dittmar, Rachel, Wang, Yuan, Tsai, Susan, Kohli, Manish, Boardman, Lisa, Patel, Tushar, Wang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726401/
https://www.ncbi.nlm.nih.gov/pubmed/26786760
http://dx.doi.org/10.1038/srep19413
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author Yuan, Tiezheng
Huang, Xiaoyi
Woodcock, Mark
Du, Meijun
Dittmar, Rachel
Wang, Yuan
Tsai, Susan
Kohli, Manish
Boardman, Lisa
Patel, Tushar
Wang, Liang
author_facet Yuan, Tiezheng
Huang, Xiaoyi
Woodcock, Mark
Du, Meijun
Dittmar, Rachel
Wang, Yuan
Tsai, Susan
Kohli, Manish
Boardman, Lisa
Patel, Tushar
Wang, Liang
author_sort Yuan, Tiezheng
collection PubMed
description 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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spelling pubmed-47264012016-01-27 Plasma extracellular RNA profiles in healthy and cancer patients Yuan, Tiezheng Huang, Xiaoyi Woodcock, Mark Du, Meijun Dittmar, Rachel Wang, Yuan Tsai, Susan Kohli, Manish Boardman, Lisa Patel, Tushar Wang, Liang Sci Rep Article 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. Nature Publishing Group 2016-01-20 /pmc/articles/PMC4726401/ /pubmed/26786760 http://dx.doi.org/10.1038/srep19413 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permissioWn from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yuan, Tiezheng
Huang, Xiaoyi
Woodcock, Mark
Du, Meijun
Dittmar, Rachel
Wang, Yuan
Tsai, Susan
Kohli, Manish
Boardman, Lisa
Patel, Tushar
Wang, Liang
Plasma extracellular RNA profiles in healthy and cancer patients
title Plasma extracellular RNA profiles in healthy and cancer patients
title_full Plasma extracellular RNA profiles in healthy and cancer patients
title_fullStr Plasma extracellular RNA profiles in healthy and cancer patients
title_full_unstemmed Plasma extracellular RNA profiles in healthy and cancer patients
title_short Plasma extracellular RNA profiles in healthy and cancer patients
title_sort plasma extracellular rna profiles in healthy and cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726401/
https://www.ncbi.nlm.nih.gov/pubmed/26786760
http://dx.doi.org/10.1038/srep19413
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