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dc.contributor.authorMoran, Barry
dc.contributor.authorO'Driscoll, Lorraine
dc.date.accessioned2021-02-15T18:17:08Z
dc.date.available2021-02-15T18:17:08Z
dc.date.issued2020
dc.date.submitted2020en
dc.identifier.citationUseckaite, Z., Mukhopadhya, A., Moran, B., O'Driscoll, L., Extracellular vesicles report on the MET status of their cells of origin regardless of the method used for their isolation., Scientific reports, 2020, 10, 1, 19020en
dc.identifier.issn2045-2322
dc.identifier.otherY
dc.identifier.urihttp://hdl.handle.net/2262/95141
dc.descriptionPUBLISHEDen
dc.description.abstractMET pathway is an important actionable target across many solid tumour types and several MET inhibitors have been developed. Extracellular vesicles (EVs) are proposed to be mini-maps of their cells of origin. However, the potential of EVs to report on the MET status of their cells of origin is unknown. After applying three proposed methods of EV separation from medium conditioned by three cell lines of known MET status, this study used an extensive range of methodologies to fundamentally characterise the resulting particles (nanoparticle tracking analysis, TEM, flow cytometry, immunoblotting) and their MET status (RT-qPCR and ELISAs). The results indicated that ultracentrifugation on density-gradient (UC-DG) consistently produced the most reliable data with regards to purest EVs. EV cargo reflected MET mRNA, total MET and pMET status of their cells of origin. In conclusion, to simply determine if the general contents of conditioned medium reflect the MET status of the conditioning cells, choice of method for initial EV separation may not be crucial. However, to be confident of specifically studying EVs and thus EV-MET cargo, UC-DG followed by extensive EV characterisation is necessary.en
dc.format.extent19020en
dc.language.isoenen
dc.relation.ispartofseriesScientific reports;
dc.relation.ispartofseries10;
dc.relation.ispartofseries1;
dc.rightsYen
dc.titleExtracellular vesicles report on the MET status of their cells of origin regardless of the method used for their isolation.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lodrisc
dc.identifier.peoplefinderurlhttp://people.tcd.ie/moranba
dc.identifier.rssinternalid222251
dc.identifier.doihttp://dx.doi.org/10.1038/s41598-020-75817-9
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeCanceren
dc.subject.TCDTagADVANCED CANCERen
dc.subject.TCDTagExtracellular Vesiclesen
dc.subject.TCDTagExtracellular vesicles (EVs)en
dc.subject.TCDTagLUNG CANCERen
dc.subject.TCDTagexosomesen
dc.identifier.rssurihttps://pubmed.ncbi.nlm.nih.gov/33149187/
dc.identifier.orcid_id0000-0002-9860-8262
dc.subject.darat_thematicHealthen
dc.status.accessibleNen
dc.contributor.sponsorIrish Research Council (IRC)en
dc.contributor.sponsorGrantNumberIRCLA/2019/49en


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