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Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells

Glioblastoma multiforme is a brain malignancy characterized by high heterogeneity, invasiveness, and resistance to current therapies, attributes related to the occurrence of glioma stem cells (GSCs). Transforming growth factor β (TGFβ) promotes self-renewal and bone morphogenetic protein (BMP) induc...

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Autores principales: Caja, Laia, Tzavlaki, Kalliopi, Dadras, Mahsa S., Tan, E-Jean, Hatem, Gad, Maturi, Naga P., Morén, Anita, Wik, Lotta, Watanabe, Yukihide, Savary, Katia, Kamali-Moghaddan, Masood, Uhrbom, Lene, Heldin, Carl-Henrik, Moustakas, Aristidis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945579/
https://www.ncbi.nlm.nih.gov/pubmed/29449696
http://dx.doi.org/10.1038/s41388-018-0136-0
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author Caja, Laia
Tzavlaki, Kalliopi
Dadras, Mahsa S.
Tan, E-Jean
Hatem, Gad
Maturi, Naga P.
Morén, Anita
Wik, Lotta
Watanabe, Yukihide
Savary, Katia
Kamali-Moghaddan, Masood
Uhrbom, Lene
Heldin, Carl-Henrik
Moustakas, Aristidis
author_facet Caja, Laia
Tzavlaki, Kalliopi
Dadras, Mahsa S.
Tan, E-Jean
Hatem, Gad
Maturi, Naga P.
Morén, Anita
Wik, Lotta
Watanabe, Yukihide
Savary, Katia
Kamali-Moghaddan, Masood
Uhrbom, Lene
Heldin, Carl-Henrik
Moustakas, Aristidis
author_sort Caja, Laia
collection PubMed
description Glioblastoma multiforme is a brain malignancy characterized by high heterogeneity, invasiveness, and resistance to current therapies, attributes related to the occurrence of glioma stem cells (GSCs). Transforming growth factor β (TGFβ) promotes self-renewal and bone morphogenetic protein (BMP) induces differentiation of GSCs. BMP7 induces the transcription factor Snail to promote astrocytic differentiation in GSCs and suppress tumor growth in vivo. We demonstrate that Snail represses stemness in GSCs. Snail interacts with SMAD signaling mediators, generates a positive feedback loop of BMP signaling and transcriptionally represses the TGFB1 gene, decreasing TGFβ1 signaling activity. Exogenous TGFβ1 counteracts Snail function in vitro, and in vivo promotes proliferation and re-expression of Nestin, confirming the importance of TGFB1 gene repression by Snail. In conclusion, novel insight highlights mechanisms whereby Snail differentially regulates the activity of the opposing BMP and TGFβ pathways, thus promoting an astrocytic fate switch and repressing stemness in GSCs.
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spelling pubmed-59455792018-05-14 Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells Caja, Laia Tzavlaki, Kalliopi Dadras, Mahsa S. Tan, E-Jean Hatem, Gad Maturi, Naga P. Morén, Anita Wik, Lotta Watanabe, Yukihide Savary, Katia Kamali-Moghaddan, Masood Uhrbom, Lene Heldin, Carl-Henrik Moustakas, Aristidis Oncogene Article Glioblastoma multiforme is a brain malignancy characterized by high heterogeneity, invasiveness, and resistance to current therapies, attributes related to the occurrence of glioma stem cells (GSCs). Transforming growth factor β (TGFβ) promotes self-renewal and bone morphogenetic protein (BMP) induces differentiation of GSCs. BMP7 induces the transcription factor Snail to promote astrocytic differentiation in GSCs and suppress tumor growth in vivo. We demonstrate that Snail represses stemness in GSCs. Snail interacts with SMAD signaling mediators, generates a positive feedback loop of BMP signaling and transcriptionally represses the TGFB1 gene, decreasing TGFβ1 signaling activity. Exogenous TGFβ1 counteracts Snail function in vitro, and in vivo promotes proliferation and re-expression of Nestin, confirming the importance of TGFB1 gene repression by Snail. In conclusion, novel insight highlights mechanisms whereby Snail differentially regulates the activity of the opposing BMP and TGFβ pathways, thus promoting an astrocytic fate switch and repressing stemness in GSCs. Nature Publishing Group UK 2018-02-16 2018 /pmc/articles/PMC5945579/ /pubmed/29449696 http://dx.doi.org/10.1038/s41388-018-0136-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Article
Caja, Laia
Tzavlaki, Kalliopi
Dadras, Mahsa S.
Tan, E-Jean
Hatem, Gad
Maturi, Naga P.
Morén, Anita
Wik, Lotta
Watanabe, Yukihide
Savary, Katia
Kamali-Moghaddan, Masood
Uhrbom, Lene
Heldin, Carl-Henrik
Moustakas, Aristidis
Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title_full Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title_fullStr Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title_full_unstemmed Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title_short Snail regulates BMP and TGFβ pathways to control the differentiation status of glioma-initiating cells
title_sort snail regulates bmp and tgfβ pathways to control the differentiation status of glioma-initiating cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945579/
https://www.ncbi.nlm.nih.gov/pubmed/29449696
http://dx.doi.org/10.1038/s41388-018-0136-0
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