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Title:RECQ1 helicase silencing decreases the tumour growth rate of U87 glioblastoma cell xenografts in zebrafish embryos
Authors:ID Vittori, Miloš (Author)
ID Breznik, Barbara (Author)
ID Hrovat, Katja (Author)
ID Kenig, Saša (Author)
ID Lah Turnšek, Tamara (Author)
Files:URL URL - Source URL, visit http://www.mdpi.com/2073-4425/8/9/222
 
.pdf PDF - Presentation file, download (2,73 MB)
MD5: AB39479285BBFF00E71B9A91F4C85613
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:RECQ1 helicase has multiple roles in DNA replication, including restoration of the replication fork and DNA repair, and plays an important role in tumour progression. Its expression is highly elevated in glioblastoma as compared to healthy brain tissue. We studied the effects of small hairpin RNA (shRNA)-induced silencing of RECQ1 helicase on the increase in cell number and the invasion of U87 glioblastoma cells. RECQ1 silencing reduced the rate of increase in the number of U87 cells by 30%. This corresponded with a 40% reduction of the percentage of cells in the G2 phase of the cell cycle, and an accumulation of cells in the G1 phase. These effects were confirmed in vivo, in the brain of zebrafish (Danio rerio) embryos, by implanting DsRed-labelled RECQ1 helicase-silenced and control U87 cells. The growth of resulting tumours was quantified by monitoring the increase in xenograft fluorescence intensity during a three-day period with fluorescence microscopy. The reduced rate of tumour growth, by approximately 30% in RECQ1 helicase-silenced cells, was in line with in vitro measurements of the increase in cell number upon RECQ1 helicase silencing. However, RECQ1 helicase silencing did not affect invasive behaviour of U87 cells in the zebrafish brain. This is the first in vivo confirmation that RECQ1 helicase is a promising molecular target in the treatment of glioblastoma.
Keywords:cancer, cell cycle, DNA damage, intravital imaging, RNA interference, theranostics
Publication status:Published
Publication version:Version of Record
Publication date:06.09.2017
Year of publishing:2017
Number of pages:str. 1-11
Numbering:Vol. 8, no. 9
PID:20.500.12556/DiRROS-19695 New window
UDC:577.2
ISSN on article:2073-4425
DOI:10.3390/genes8090222 New window
COBISS.SI-ID:4411215 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 7. 9. 2017;
Publication date in DiRROS:25.07.2024
Views:337
Downloads:227
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Record is a part of a journal

Title:Genes
Shortened title:Genes
Publisher:Multidisciplinary Digital Publishing Institute (MDPI)
ISSN:2073-4425
COBISS.SI-ID:523100185 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0245-2015
Name:Ekotoksiologija, toksikološka genomika in karcinogeneza

Funder:EC - European Commission
Funding programme:INTERREG project
Project number:42, 2011
Acronym:GLIOMA

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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