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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4726401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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