生物
胶质母细胞瘤
癌症研究
整合素
生物信息学
细胞
遗传学
作者
Tobias L. Haas,Maria Rita Sciuto,Lidia Brunetto,Cecilia Valvo,Michele Signore,Micol Eleonora Fiori,Simona Di Martino,Stefano Giannetti,Liliana Morgante,Alessandra Boe,Michele Patrizii,Uwe Warnken,Martina Schnölzer,Andrea Ciolfi,Chiara Di Stefano,Mauro Biffoni,Lucia Ricci‐Vitiani,Roberto Pallini,Ruggero De Maria
出处
期刊:Cell Stem Cell
[Elsevier]
日期:2017-06-10
卷期号:21 (1): 35-50.e9
被引量:108
标识
DOI:10.1016/j.stem.2017.04.009
摘要
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.
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