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Methodical optimization of exosomal microRNA izolation from cerebrospinal fluid of glioma patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F24%3AN0000174" target="_blank" >RIV/00027162:_____/24:N0000174 - isvavai.cz</a>

  • Alternative codes found

    RIV/00027162:_____/24:N0000175

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Methodical optimization of exosomal microRNA izolation from cerebrospinal fluid of glioma patients

  • Original language description

    Poster. Abstrakt v publikaci: ASEV-CzeSEV joint meeting on Extracellular Vesicles, 16. – 17. 9. 2024, Vídeň, Rakousko; ISBN 978-80-11-05123-5, [P14]. Our project is focused on creating a diagnostic panel of exosomal microRNA from cerebrospinal fluid (CSF) for predicting the diagnosis and therapeutic response in glioma patients. The first step of this study was to optimize a method for isolating extracellular vesicles (EVs) circulating in the CSF. To compare EV isolation methods, CSF from four patients with hydrocephalus, from whom higher sample volumes could be obtained, was used. To exclude the influence of freezing during sample storage, half of each sample was frozen at -80°C and the other half was used immediately after collection. Three methods were used for EV isolation: ultracentrifugation, Plasma/Serum Exosome Purification Kit (Norgen), and ExoDisk™ (LabSpinner). The quantity and size of the isolated particles were measured using the ZetaSizer Ultra and particle visualization was performed using a transmission electron microscope (TEM). The particles were further characterized using the cytometer CellStream with the CD63 specific fluorescent labeling. Ultracentrifugation proved to be the most suitable method for isolating EVs from CSF, as it yielded the highest quality and specificity of isolated particles, which were not affected by freezing the CSF before isolation. In the next step, the lysis of exosomes using three miRNA isolation kits was compared: mirVana™ Isolation Kit (Invitrogen), Urine microRNA Purification Kit (Norgen), and miRNeasy Serum/Plasma Kit (QIAGEN). The efficiency of the lysis buffers was analyzed on the ZetaSizer Ultra and visualized with TEM. Based on the results, the QIAGEN isolation kit was selected for further experimental work.Supported by AZV NU22-03-00290 and DKRVO RO0524.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

    <a href="/en/project/NU22-03-00290" target="_blank" >NU22-03-00290: Study on exosomal microRNAs in gliomas: implications for diagnostics and innovative therapy</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů