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YAP controls cell migration and invasion through a Rho-GTPase switch

Sagar R. Shah, Nathaniel D. Tippens, JinSeok Park, Ahmed Mohyeldin, Shuyan Wang, Guillermo Vela, Juan C. Martinez-Gutierrez, Seth S. Margolis, Susanne Schmidt, Shuli Xia, Andre Levchenko, Alfredo Quiñones-Hinojosa
doi: https://doi.org/10.1101/602052
Sagar R. Shah
1Departments of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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Nathaniel D. Tippens
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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JinSeok Park
1Departments of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
6CRBM-CNRS, University of Montpellier, 1919 route de Mende, 34293 Montpellier, France
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Ahmed Mohyeldin
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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Shuyan Wang
5Department of Neurology, Kennedy Krieger Institute, Baltimore, MD 21231, USA
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Guillermo Vela
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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Juan C. Martinez-Gutierrez
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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Seth S. Margolis
3Departments of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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Susanne Schmidt
6CRBM-CNRS, University of Montpellier, 1919 route de Mende, 34293 Montpellier, France
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Shuli Xia
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Andre Levchenko
1Departments of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
7Department of Biomedical Engineering and Yale Systems Biology Institute, Yale University, New Haven, CT, USA
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  • For correspondence: Quinones-Hinojosa.Alfredo@mayo.edu andre.levchenko@yale.edu
Alfredo Quiñones-Hinojosa
2Departments of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
4Departments of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
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  • For correspondence: Quinones-Hinojosa.Alfredo@mayo.edu andre.levchenko@yale.edu
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SUMMARY

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.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted April 08, 2019.
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YAP controls cell migration and invasion through a Rho-GTPase switch
Sagar R. Shah, Nathaniel D. Tippens, JinSeok Park, Ahmed Mohyeldin, Shuyan Wang, Guillermo Vela, Juan C. Martinez-Gutierrez, Seth S. Margolis, Susanne Schmidt, Shuli Xia, Andre Levchenko, Alfredo Quiñones-Hinojosa
bioRxiv 602052; doi: https://doi.org/10.1101/602052
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YAP controls cell migration and invasion through a Rho-GTPase switch
Sagar R. Shah, Nathaniel D. Tippens, JinSeok Park, Ahmed Mohyeldin, Shuyan Wang, Guillermo Vela, Juan C. Martinez-Gutierrez, Seth S. Margolis, Susanne Schmidt, Shuli Xia, Andre Levchenko, Alfredo Quiñones-Hinojosa
bioRxiv 602052; doi: https://doi.org/10.1101/602052

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