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miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development
by
Chen, Clark C.
, Carter, Bob S.
, Mao, Ying
, Breakefield, Xandra O.
, Akers, Johnny C.
, Van Meir, Erwin G.
, Kalinina, Juliya
, Pingle, Sandeep
, Kim, Ryan
, Ramakrishnan, Valya
, Nakano, Ichiro
, Hua, Wei
, Hochberg, Fred H.
, Skog, Johan
, Kesari, Santosh
in
Biomarkers
/ Biomarkers, Tumor - cerebrospinal fluid
/ Brain cancer
/ Cell Line, Tumor
/ Cell lines
/ Cerebrospinal fluid
/ Cerebrospinal Fluid - metabolism
/ Consent
/ Electronic filing
/ Extracellular vesicles
/ Glioblastoma
/ Glioblastoma - genetics
/ Glioblastoma cells
/ Glyceraldehyde-3-phosphate dehydrogenase
/ Hematology
/ Hospitals
/ Humans
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Neurosciences
/ Neurosurgery
/ NMR
/ Nuclear magnetic resonance
/ Oncology
/ Patients
/ Reverse Transcriptase Polymerase Chain Reaction
/ RNA, Ribosomal, 18S - genetics
/ rRNA 18S
/ Vesicles
2013
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miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development
by
Chen, Clark C.
, Carter, Bob S.
, Mao, Ying
, Breakefield, Xandra O.
, Akers, Johnny C.
, Van Meir, Erwin G.
, Kalinina, Juliya
, Pingle, Sandeep
, Kim, Ryan
, Ramakrishnan, Valya
, Nakano, Ichiro
, Hua, Wei
, Hochberg, Fred H.
, Skog, Johan
, Kesari, Santosh
in
Biomarkers
/ Biomarkers, Tumor - cerebrospinal fluid
/ Brain cancer
/ Cell Line, Tumor
/ Cell lines
/ Cerebrospinal fluid
/ Cerebrospinal Fluid - metabolism
/ Consent
/ Electronic filing
/ Extracellular vesicles
/ Glioblastoma
/ Glioblastoma - genetics
/ Glioblastoma cells
/ Glyceraldehyde-3-phosphate dehydrogenase
/ Hematology
/ Hospitals
/ Humans
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Neurosciences
/ Neurosurgery
/ NMR
/ Nuclear magnetic resonance
/ Oncology
/ Patients
/ Reverse Transcriptase Polymerase Chain Reaction
/ RNA, Ribosomal, 18S - genetics
/ rRNA 18S
/ Vesicles
2013
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miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development
by
Chen, Clark C.
, Carter, Bob S.
, Mao, Ying
, Breakefield, Xandra O.
, Akers, Johnny C.
, Van Meir, Erwin G.
, Kalinina, Juliya
, Pingle, Sandeep
, Kim, Ryan
, Ramakrishnan, Valya
, Nakano, Ichiro
, Hua, Wei
, Hochberg, Fred H.
, Skog, Johan
, Kesari, Santosh
in
Biomarkers
/ Biomarkers, Tumor - cerebrospinal fluid
/ Brain cancer
/ Cell Line, Tumor
/ Cell lines
/ Cerebrospinal fluid
/ Cerebrospinal Fluid - metabolism
/ Consent
/ Electronic filing
/ Extracellular vesicles
/ Glioblastoma
/ Glioblastoma - genetics
/ Glioblastoma cells
/ Glyceraldehyde-3-phosphate dehydrogenase
/ Hematology
/ Hospitals
/ Humans
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Neurosciences
/ Neurosurgery
/ NMR
/ Nuclear magnetic resonance
/ Oncology
/ Patients
/ Reverse Transcriptase Polymerase Chain Reaction
/ RNA, Ribosomal, 18S - genetics
/ rRNA 18S
/ Vesicles
2013
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miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development
Journal Article
miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development
2013
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Overview
Glioblastoma cells secrete extra-cellular vesicles (EVs) containing microRNAs (miRNAs). Analysis of these EV miRNAs in the bio-fluids of afflicted patients represents a potential platform for biomarker development. However, the analytic algorithm for quantitative assessment of EV miRNA remains under-developed. Here, we demonstrate that the reference transcripts commonly used for quantitative PCR (including GAPDH, 18S rRNA, and hsa-miR-103) were unreliable for assessing EV miRNA. In this context, we quantitated EV miRNA in absolute terms and normalized this value to the input EV number. Using this method, we examined the abundance of miR-21, a highly over-expressed miRNA in glioblastomas, in EVs. In a panel of glioblastoma cell lines, the cellular levels of miR-21 correlated with EV miR-21 levels (p<0.05), suggesting that glioblastoma cells actively secrete EVs containing miR-21. Consistent with this hypothesis, the CSF EV miR-21 levels of glioblastoma patients (n=13) were, on average, ten-fold higher than levels in EVs isolated from the CSF of non-oncologic patients (n=13, p<0.001). Notably, none of the glioblastoma CSF harbored EV miR-21 level below 0.25 copies per EV in this cohort. Using this cut-off value, we were able to prospectively distinguish CSF derived from glioblastoma and non-oncologic patients in an independent cohort of twenty-nine patients (Sensitivity=87%; Specificity=93%; AUC=0.91, p<0.01). Our results suggest that CSF EV miRNA analysis of miR-21 may serve as a platform for glioblastoma biomarker development.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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