Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation.
Adult
Body Fluids
/ chemistry
Cell Line
Cell-Free Nucleic Acids
/ isolation & purification
Circulating MicroRNA
/ isolation & purification
Extracellular Vesicles
/ metabolism
Female
Healthy Volunteers
Humans
Male
MicroRNAs
/ isolation & purification
RNA
/ isolation & purification
Reproducibility of Results
Sequence Analysis, RNA
/ methods
extracellular RNA
extracellular vesicles
lipoprotein
ribonucleoprotein
Journal
Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066
Informations de publication
Date de publication:
04 04 2019
04 04 2019
Historique:
received:
03
08
2018
revised:
29
12
2018
accepted:
11
03
2019
entrez:
6
4
2019
pubmed:
6
4
2019
medline:
25
1
2020
Statut:
ppublish
Résumé
Poor reproducibility within and across studies arising from lack of knowledge regarding the performance of extracellular RNA (exRNA) isolation methods has hindered progress in the exRNA field. A systematic comparison of 10 exRNA isolation methods across 5 biofluids revealed marked differences in the complexity and reproducibility of the resulting small RNA-seq profiles. The relative efficiency with which each method accessed different exRNA carrier subclasses was determined by estimating the proportions of extracellular vesicle (EV)-, ribonucleoprotein (RNP)-, and high-density lipoprotein (HDL)-specific miRNA signatures in each profile. An interactive web-based application (miRDaR) was developed to help investigators select the optimal exRNA isolation method for their studies. miRDar provides comparative statistics for all expressed miRNAs or a selected subset of miRNAs in the desired biofluid for each exRNA isolation method and returns a ranked list of exRNA isolation methods prioritized by complexity, expression level, and reproducibility. These results will improve reproducibility and stimulate further progress in exRNA biomarker development.
Identifiants
pubmed: 30951671
pii: S0092-8674(19)30286-7
doi: 10.1016/j.cell.2019.03.024
pmc: PMC6557167
mid: NIHMS1021236
pii:
doi:
Substances chimiques
Cell-Free Nucleic Acids
0
Circulating MicroRNA
0
MicroRNAs
0
RNA
63231-63-0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
446-462.e16Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL122547
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA069246
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217685
Pays : United States
Organisme : NCATS NIH HHS
ID : UH3 TR000943
Pays : United States
Organisme : NIDA NIH HHS
ID : U54 DA036134
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL133575
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA217833
Pays : United States
Organisme : NCI NIH HHS
ID : U19 CA179563
Pays : United States
Organisme : NCATS NIH HHS
ID : UH3 TR000901
Pays : United States
Organisme : NCATS NIH HHS
ID : UH3 TR000890
Pays : United States
Organisme : NCI NIH HHS
ID : U19 CA179512
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR000901
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL127099
Pays : United States
Organisme : NCATS NIH HHS
ID : UH3 TR000906
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR000884
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR000906
Pays : United States
Organisme : NICHD NIH HHS
ID : T32 HD007203
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR000943
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR000890
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA209904
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL126494
Pays : United States
Organisme : NCATS NIH HHS
ID : UH3 TR000884
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.
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