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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Meta-analysis and experimental validation identified FREM2 and SPRY1 as new glioblastoma marker candidates</dc:title><dc:creator>Vidak,	Marko	(Avtor)
	</dc:creator><dc:creator>Jovchevska,	Ivana	(Avtor)
	</dc:creator><dc:creator>Šamec,	Neja	(Avtor)
	</dc:creator><dc:creator>Zottel,	Alja	(Avtor)
	</dc:creator><dc:creator>Liović,	Mirjana	(Avtor)
	</dc:creator><dc:creator>Rozman,	Damjana	(Avtor)
	</dc:creator><dc:creator>Džeroski,	Sašo	(Avtor)
	</dc:creator><dc:creator>Juvan,	Peter	(Avtor)
	</dc:creator><dc:creator>Komel,	Radovan	(Avtor)
	</dc:creator><dc:subject>glioblastoma</dc:subject><dc:subject>glioblastoma stem cells</dc:subject><dc:subject>biomarkers</dc:subject><dc:subject>data repositories</dc:subject><dc:subject>meta-analysis</dc:subject><dc:subject>cell surface</dc:subject><dc:subject>experimental validation</dc:subject><dc:subject>FREM2</dc:subject><dc:subject>SPRY1</dc:subject><dc:description>Glioblastoma (GB) is the most aggressive brain malignancy. Although some potential glioblastoma biomarkers have already been identified, there is a lack of cell membrane-bound biomarkers capable of distinguishing brain tissue from glioblastoma and/or glioblastoma stem cells (GSC), which are responsible for the rapid post-operative tumor reoccurrence. In order to find new GB/GSC marker candidates that would be cell surface proteins (CSP), we have performed meta-analysis of genome-scale mRNA expression data from three data repositories (GEO, ArrayExpress and GLIOMASdb). The search yielded ten appropriate datasets, and three (GSE4290/GDS1962, GSE23806/GDS3885, and GLIOMASdb) were used for selection of new GB/GSC marker candidates, while the other seven (GSE4412/GDS1975, GSE4412/GDS1976, E-GEOD-52009, E-GEOD-68848, E-GEOD-16011, E-GEOD-4536, and E-GEOD-74571) were used for bioinformatic validation. The selection identified four new CSP-encoding candidate genes-CD276, FREM2, SPRY1, and SLC47A1-and the bioinformatic validation confirmed these findings. A review of the literature revealed that CD276 is not a novel candidate, while SLC47A1 had lower validation test scores than the other new candidates and was therefore not considered for experimental validation. This validation revealed that the expression of FREM2-but not SPRY1-is higher in glioblastoma cell lines when compared to non-malignant astrocytes. In addition, FREM2 gene and protein expression levels are higher in GB stem-like cell lines than in conventional glioblastoma cell lines. FREM2 is thus proposed as a novel GB biomarker and a putative biomarker of glioblastoma stem cells. Both FREM2 and SPRY1 are expressed on the surface of the GB cells, while SPRY1 alone was found overexpressed in the cytosol of non-malignant astrocytes.</dc:description><dc:date>2018</dc:date><dc:date>2021-10-04 14:52:35</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>131851</dc:identifier><dc:identifier>UDK: 577</dc:identifier><dc:identifier>ISSN pri članku: 1422-0067</dc:identifier><dc:identifier>DOI: 10.3390/ijms19051369</dc:identifier><dc:identifier>COBISS_ID: 33752793</dc:identifier><dc:language>sl</dc:language></metadata>
