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Silencing of carbonic anhydrase I enhances the malignant potential of exosomes secreted by prostatic tumour cells
R. Bánová Vulić, M. Zdurienčíková, S. Tyčiaková, O. Benada, M. Dubrovčáková, J. Lakota, Ľ. Škultéty,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2012
Free Medical Journals
od 2000
PubMed Central
od 2000
Europe PubMed Central
od 2000 do 2020
ProQuest Central
od 2000-07-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2012-01-01
Medline Complete (EBSCOhost)
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-07-01
Wiley-Blackwell Open Access Titles
od 2000
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
30916466
DOI
10.1111/jcmm.14265
Knihovny.cz E-zdroje
- MeSH
- buňky PC-3 MeSH
- energetický metabolismus genetika MeSH
- exozómy genetika metabolismus MeSH
- karboanhydrasa I genetika metabolismus MeSH
- lidé MeSH
- nádory prostaty genetika metabolismus patologie MeSH
- pohyb buněk genetika MeSH
- proliferace buněk genetika MeSH
- regulace genové exprese enzymů * MeSH
- regulace genové exprese u nádorů * MeSH
- RNA interference * MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
We report results showing that the silencing of carbonic anhydrase I (siCA1) in prostatic (PC3) tumour cells has a significant impact on exosome formation. An increased diameter, concentration and diversity of the produced exosomes were noticed as a consequence of this knock-down. The protein composition of the exosomes' cargo was also altered. Liquid chromatography and mass spectrometry analyses identified 42 proteins significantly altered in PC3 siCA1 exosomes compared with controls. The affected proteins are mainly involved in metabolic processes, biogenesis, cell component organization and defense/immunity. Interestingly, almost all of them have been described as 'enhancers' of tumour development through the promotion of cell proliferation, migration and invasion. Thus, our results indicate that the reduced expression of the CA1 protein enhances the malignant potential of PC3 cells.
Biomedical Research Center SAS Bratislava Slovak Republic
Institute of Microbiology of the CAS v v i Prague Czech Republic
Citace poskytuje Crossref.org
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