| Literature DB >> 28602620 |
Tobias L Haas1, Maria Rita Sciuto2, Lidia Brunetto2, Cecilia Valvo3, Michele Signore2, Micol E Fiori3, Simona di Martino4, Stefano Giannetti5, Liliana Morgante5, Alessandra Boe2, Michele Patrizii2, Uwe Warnken6, Martina Schnölzer6, Andrea Ciolfi7, Chiara Di Stefano2, Mauro Biffoni2, Lucia Ricci-Vitiani2, Roberto Pallini8, Ruggero De Maria9.
Abstract
Functionally relevant markers of glioblastoma stem-like cells (GSCs) have potential for therapeutic targeting to treat this aggressive disease. Here we used generation and screening of thousands of monoclonal antibodies to search for receptors and signaling pathways preferentially enriched in GSCs. We identified integrin α7 (ITGA7) as a major laminin receptor in GSCs and in primary high-grade glioma specimens. Analyses of mRNA profiles in comprehensive datasets revealed that high ITGA7 expression negatively correlated with survival of patients with both low- and high-grade glioma. In vitro and in vivo analyses showed that ITGA7 plays a key functional role in growth and invasiveness of GSCs. We also found that targeting of ITGA7 by RNAi or blocking mAbs impaired laminin-induced signaling, and it led to a significant delay in tumor engraftment plus a strong reduction in tumor size and invasion. Our data, therefore, highlight ITGA7 as a glioblastoma biomarker and candidate therapeutic target.Entities:
Keywords: biomarker; cancer stem cell marker; glioblastoma cell invasion; high throughput screening; mAb; monoclonal antibody
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Year: 2017 PMID: 28602620 DOI: 10.1016/j.stem.2017.04.009
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633