author_facet Augustin, Iris
Goidts, Violaine
Bongers, Angelika
Kerr, Grainne
Vollert, Gordon
Radlwimmer, Bernhard
Hartmann, Christian
Herold‐Mende, Christel
Reifenberger, Guido
von Deimling, Andreas
Boutros, Michael
Augustin, Iris
Goidts, Violaine
Bongers, Angelika
Kerr, Grainne
Vollert, Gordon
Radlwimmer, Bernhard
Hartmann, Christian
Herold‐Mende, Christel
Reifenberger, Guido
von Deimling, Andreas
Boutros, Michael
author Augustin, Iris
Goidts, Violaine
Bongers, Angelika
Kerr, Grainne
Vollert, Gordon
Radlwimmer, Bernhard
Hartmann, Christian
Herold‐Mende, Christel
Reifenberger, Guido
von Deimling, Andreas
Boutros, Michael
spellingShingle Augustin, Iris
Goidts, Violaine
Bongers, Angelika
Kerr, Grainne
Vollert, Gordon
Radlwimmer, Bernhard
Hartmann, Christian
Herold‐Mende, Christel
Reifenberger, Guido
von Deimling, Andreas
Boutros, Michael
EMBO Molecular Medicine
The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
Molecular Medicine
author_sort augustin, iris
spelling Augustin, Iris Goidts, Violaine Bongers, Angelika Kerr, Grainne Vollert, Gordon Radlwimmer, Bernhard Hartmann, Christian Herold‐Mende, Christel Reifenberger, Guido von Deimling, Andreas Boutros, Michael 1757-4676 1757-4684 Springer Science and Business Media LLC Molecular Medicine http://dx.doi.org/10.1002/emmm.201100186 <jats:title>Abstract</jats:title><jats:p>Malignant astrocytomas are highly aggressive brain tumours with poor prognosis. While a number of structural genomic changes and dysregulation of signalling pathways in gliomas have been described, the identification of biomarkers and druggable targets remains an important task for novel diagnostic and therapeutic approaches. Here, we show that the Wnt‐specific secretory protein Evi (also known as GPR177/Wntless/Sprinter) is overexpressed in astrocytic gliomas. Evi/Wls is a core Wnt signalling component and a specific regulator of pan‐Wnt protein secretion, affecting both canonical and non‐canonical signalling. We demonstrate that its depletion in glioma and glioma‐derived stem‐like cells led to decreased cell proliferation and apoptosis. Furthermore, Evi/Wls silencing in glioma cells reduced cell migration and the capacity to form tumours <jats:italic>in vivo</jats:italic>. We further show that Evi/Wls overexpression is sufficient to promote downstream Wnt signalling. Taken together, our study identifies Evi/Wls as an essential regulator of glioma tumourigenesis, identifying a pathway‐specific protein trafficking factor as an oncogene and offering novel therapeutic options to interfere with the aberrant regulation of growth factors at the site of production.</jats:p> The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis EMBO Molecular Medicine
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title The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_unstemmed The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_full The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_fullStr The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_full_unstemmed The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_short The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_sort the wnt secretion protein evi/gpr177 promotes glioma tumourigenesis
topic Molecular Medicine
url http://dx.doi.org/10.1002/emmm.201100186
publishDate 2012
physical 38-51
description <jats:title>Abstract</jats:title><jats:p>Malignant astrocytomas are highly aggressive brain tumours with poor prognosis. While a number of structural genomic changes and dysregulation of signalling pathways in gliomas have been described, the identification of biomarkers and druggable targets remains an important task for novel diagnostic and therapeutic approaches. Here, we show that the Wnt‐specific secretory protein Evi (also known as GPR177/Wntless/Sprinter) is overexpressed in astrocytic gliomas. Evi/Wls is a core Wnt signalling component and a specific regulator of pan‐Wnt protein secretion, affecting both canonical and non‐canonical signalling. We demonstrate that its depletion in glioma and glioma‐derived stem‐like cells led to decreased cell proliferation and apoptosis. Furthermore, Evi/Wls silencing in glioma cells reduced cell migration and the capacity to form tumours <jats:italic>in vivo</jats:italic>. We further show that Evi/Wls overexpression is sufficient to promote downstream Wnt signalling. Taken together, our study identifies Evi/Wls as an essential regulator of glioma tumourigenesis, identifying a pathway‐specific protein trafficking factor as an oncogene and offering novel therapeutic options to interfere with the aberrant regulation of growth factors at the site of production.</jats:p>
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author Augustin, Iris, Goidts, Violaine, Bongers, Angelika, Kerr, Grainne, Vollert, Gordon, Radlwimmer, Bernhard, Hartmann, Christian, Herold‐Mende, Christel, Reifenberger, Guido, von Deimling, Andreas, Boutros, Michael
author_facet Augustin, Iris, Goidts, Violaine, Bongers, Angelika, Kerr, Grainne, Vollert, Gordon, Radlwimmer, Bernhard, Hartmann, Christian, Herold‐Mende, Christel, Reifenberger, Guido, von Deimling, Andreas, Boutros, Michael, Augustin, Iris, Goidts, Violaine, Bongers, Angelika, Kerr, Grainne, Vollert, Gordon, Radlwimmer, Bernhard, Hartmann, Christian, Herold‐Mende, Christel, Reifenberger, Guido, von Deimling, Andreas, Boutros, Michael
author_sort augustin, iris
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description <jats:title>Abstract</jats:title><jats:p>Malignant astrocytomas are highly aggressive brain tumours with poor prognosis. While a number of structural genomic changes and dysregulation of signalling pathways in gliomas have been described, the identification of biomarkers and druggable targets remains an important task for novel diagnostic and therapeutic approaches. Here, we show that the Wnt‐specific secretory protein Evi (also known as GPR177/Wntless/Sprinter) is overexpressed in astrocytic gliomas. Evi/Wls is a core Wnt signalling component and a specific regulator of pan‐Wnt protein secretion, affecting both canonical and non‐canonical signalling. We demonstrate that its depletion in glioma and glioma‐derived stem‐like cells led to decreased cell proliferation and apoptosis. Furthermore, Evi/Wls silencing in glioma cells reduced cell migration and the capacity to form tumours <jats:italic>in vivo</jats:italic>. We further show that Evi/Wls overexpression is sufficient to promote downstream Wnt signalling. Taken together, our study identifies Evi/Wls as an essential regulator of glioma tumourigenesis, identifying a pathway‐specific protein trafficking factor as an oncogene and offering novel therapeutic options to interfere with the aberrant regulation of growth factors at the site of production.</jats:p>
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spelling Augustin, Iris Goidts, Violaine Bongers, Angelika Kerr, Grainne Vollert, Gordon Radlwimmer, Bernhard Hartmann, Christian Herold‐Mende, Christel Reifenberger, Guido von Deimling, Andreas Boutros, Michael 1757-4676 1757-4684 Springer Science and Business Media LLC Molecular Medicine http://dx.doi.org/10.1002/emmm.201100186 <jats:title>Abstract</jats:title><jats:p>Malignant astrocytomas are highly aggressive brain tumours with poor prognosis. While a number of structural genomic changes and dysregulation of signalling pathways in gliomas have been described, the identification of biomarkers and druggable targets remains an important task for novel diagnostic and therapeutic approaches. Here, we show that the Wnt‐specific secretory protein Evi (also known as GPR177/Wntless/Sprinter) is overexpressed in astrocytic gliomas. Evi/Wls is a core Wnt signalling component and a specific regulator of pan‐Wnt protein secretion, affecting both canonical and non‐canonical signalling. We demonstrate that its depletion in glioma and glioma‐derived stem‐like cells led to decreased cell proliferation and apoptosis. Furthermore, Evi/Wls silencing in glioma cells reduced cell migration and the capacity to form tumours <jats:italic>in vivo</jats:italic>. We further show that Evi/Wls overexpression is sufficient to promote downstream Wnt signalling. Taken together, our study identifies Evi/Wls as an essential regulator of glioma tumourigenesis, identifying a pathway‐specific protein trafficking factor as an oncogene and offering novel therapeutic options to interfere with the aberrant regulation of growth factors at the site of production.</jats:p> The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis EMBO Molecular Medicine
spellingShingle Augustin, Iris, Goidts, Violaine, Bongers, Angelika, Kerr, Grainne, Vollert, Gordon, Radlwimmer, Bernhard, Hartmann, Christian, Herold‐Mende, Christel, Reifenberger, Guido, von Deimling, Andreas, Boutros, Michael, EMBO Molecular Medicine, The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis, Molecular Medicine
title The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_full The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_fullStr The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_full_unstemmed The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_short The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
title_sort the wnt secretion protein evi/gpr177 promotes glioma tumourigenesis
title_unstemmed The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis
topic Molecular Medicine
url http://dx.doi.org/10.1002/emmm.201100186