MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]

MicroRNAs are non-coding RNAs that negatively regulate mRNA expression and play significant roles in both health and disease. Differential microRNA expression has been used to aid diagnosis and discriminate disease stages. The accuracy and reliability of microRNA expression measurement is of utmost...

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Main Authors: Sadaf Atarod, Hannah Smith, Anne Dickinson, Xiao-Nong Wang
Format: Article
Language:English
Published: F1000 Research Ltd 2015-06-01
Series:F1000Research
Subjects:
Online Access:http://f1000research.com/articles/3-183/v3
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spelling doaj-3eeb5709be5640b9b24a73973b1c15f52020-11-25T03:24:42ZengF1000 Research LtdF1000Research2046-14022015-06-01310.12688/f1000research.4884.37159MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]Sadaf Atarod0Hannah Smith1Anne Dickinson2Xiao-Nong Wang3Haematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UKHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UKHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UKHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UKMicroRNAs are non-coding RNAs that negatively regulate mRNA expression and play significant roles in both health and disease. Differential microRNA expression has been used to aid diagnosis and discriminate disease stages. The accuracy and reliability of microRNA expression measurement is of utmost importance. Quantification of microRNA expression in human peripheral blood is commonly detected using total RNA extracted via different methods. To date, no convincing data are available showing whether microRNA quantification results can be influenced by the use of total RNA extracted from whole blood or peripheral blood mononuclear cells (PBMCs). This study examined miR-146a-5p and miR-155-5p expression using total RNA extracted in parallel from whole blood and PBMCs of 14 healthy volunteers. The data showed that the quantification of miRNA using total RNA extracted from whole blood varied from that of PBMCs, indicating that the miRNA expression was a result of all the different cell-types present in whole blood. Our results suggested that the source of total RNA and the statistical analyses performed are crucial considerations when designing miRNA research.http://f1000research.com/articles/3-183/v3Methods for Diagnostic & Therapeutic Studies
collection DOAJ
language English
format Article
sources DOAJ
author Sadaf Atarod
Hannah Smith
Anne Dickinson
Xiao-Nong Wang
spellingShingle Sadaf Atarod
Hannah Smith
Anne Dickinson
Xiao-Nong Wang
MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
F1000Research
Methods for Diagnostic & Therapeutic Studies
author_facet Sadaf Atarod
Hannah Smith
Anne Dickinson
Xiao-Nong Wang
author_sort Sadaf Atarod
title MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
title_short MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
title_full MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
title_fullStr MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
title_full_unstemmed MicroRNA levels quantified in whole blood varies from PBMCs [version 3; referees: 2 approved, 1 not approved]
title_sort microrna levels quantified in whole blood varies from pbmcs [version 3; referees: 2 approved, 1 not approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2015-06-01
description MicroRNAs are non-coding RNAs that negatively regulate mRNA expression and play significant roles in both health and disease. Differential microRNA expression has been used to aid diagnosis and discriminate disease stages. The accuracy and reliability of microRNA expression measurement is of utmost importance. Quantification of microRNA expression in human peripheral blood is commonly detected using total RNA extracted via different methods. To date, no convincing data are available showing whether microRNA quantification results can be influenced by the use of total RNA extracted from whole blood or peripheral blood mononuclear cells (PBMCs). This study examined miR-146a-5p and miR-155-5p expression using total RNA extracted in parallel from whole blood and PBMCs of 14 healthy volunteers. The data showed that the quantification of miRNA using total RNA extracted from whole blood varied from that of PBMCs, indicating that the miRNA expression was a result of all the different cell-types present in whole blood. Our results suggested that the source of total RNA and the statistical analyses performed are crucial considerations when designing miRNA research.
topic Methods for Diagnostic & Therapeutic Studies
url http://f1000research.com/articles/3-183/v3
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