RT Journal Article SR Electronic T1 YAP controls cell migration and invasion through a Rho-GTPase switch JF bioRxiv FD Cold Spring Harbor Laboratory SP 602052 DO 10.1101/602052 A1 Sagar R. Shah A1 Nathaniel D. Tippens A1 JinSeok Park A1 Ahmed Mohyeldin A1 Shuyan Wang A1 Guillermo Vela A1 Juan C. Martinez-Gutierrez A1 Seth S. Margolis A1 Susanne Schmidt A1 Shuli Xia A1 Andre Levchenko A1 Alfredo QuiƱones-Hinojosa YR 2019 UL http://biorxiv.org/content/early/2019/04/08/602052.abstract AB Understanding the mechanisms controlling invasive spread of normal and transformed cells is central to understanding diverse processes including cancer progression. Here, we report that Yes-associated protein (YAP), a central transcriptional regulator implicated in controlling organ and body size, modulates a Rho-GTPase switch that drives cellular migration by directly transactivating the Rac1-GEF protein TRIO. Additionally, YAP and TRIO activate STAT3 to promote invasive behavior. While we find this YAP-dependent infiltrative program in many cell types, it is particularly enhanced in a patient specific way in the most common malignant brain tumor, glioblastoma (GBM), where hyperactivation of the YAP-mediated TRIO and STAT3 network also confers poor patient outcome and up-regulation of genes associated with the Mesenchymal subtype of GBM. Our analysis suggests that the YAP-TRIO-STAT3 signaling network identified in this study is a ubiquitous regulator of invasive cell spread in a variety of normal and pathological contexts.