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Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model

Glioblastoma Multiforme (GBM) is the most common form of malignant brain tumor with poor prognosis. Amplification of Epidermal Growth Factor Receptor (EGFR), and mutations leading to activation of Phosphatidyl-Inositol-3 Kinase (PI3K) pathway are commonly associated with GBM. Using a previously publ...

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Autores principales: Gangwani, Karishma, Snigdha, Kirti, Kango-Singh, Madhuri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225285/
https://www.ncbi.nlm.nih.gov/pubmed/32457905
http://dx.doi.org/10.3389/fcell.2020.00306
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author Gangwani, Karishma
Snigdha, Kirti
Kango-Singh, Madhuri
author_facet Gangwani, Karishma
Snigdha, Kirti
Kango-Singh, Madhuri
author_sort Gangwani, Karishma
collection PubMed
description Glioblastoma Multiforme (GBM) is the most common form of malignant brain tumor with poor prognosis. Amplification of Epidermal Growth Factor Receptor (EGFR), and mutations leading to activation of Phosphatidyl-Inositol-3 Kinase (PI3K) pathway are commonly associated with GBM. Using a previously published Drosophila glioma model generated by coactivation of PI3K and EGFR pathways [by downregulation of Pten and overexpression of oncogenic Ras] in glial cells, we showed that the Drosophila Tep1 gene (ortholog of human CD109) regulates Yki (the Drosophila ortholog of human YAP/TAZ) via an evolutionarily conserved mechanism. Oncogenic signaling by the YAP/TAZ pathway occurs in cells that acquire CD109 expression in response to the inflammatory environment induced by radiation in clinically relevant models. Further, downregulation of Tep1 caused a reduction in Yki activity and reduced glioma growth. A key function of Yki in larval CNS is stem cell renewal and formation of neuroblasts. Other reports suggest different upstream regulators of Yki activity in the optic lobe versus the central brain regions of the larval CNS. We hypothesized that Tep1 interacts with the Hippo pathway effector Yki to regulate neuroblast numbers. We tested if Tep1 acts through Yki to affect glioma growth, and if in normal cells Tep1 affects neuroblast number and proliferation. Our data suggests that Tep1 affects Yki mediated stem cell renewal in glioma, as reduction of Tep significantly decreases the number of neuroblasts in glioma. Thus, we identify Tep1-Yki interaction in the larval CNS that plays a key role in glioma growth and progression.
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spelling pubmed-72252852020-05-25 Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model Gangwani, Karishma Snigdha, Kirti Kango-Singh, Madhuri Front Cell Dev Biol Cell and Developmental Biology Glioblastoma Multiforme (GBM) is the most common form of malignant brain tumor with poor prognosis. Amplification of Epidermal Growth Factor Receptor (EGFR), and mutations leading to activation of Phosphatidyl-Inositol-3 Kinase (PI3K) pathway are commonly associated with GBM. Using a previously published Drosophila glioma model generated by coactivation of PI3K and EGFR pathways [by downregulation of Pten and overexpression of oncogenic Ras] in glial cells, we showed that the Drosophila Tep1 gene (ortholog of human CD109) regulates Yki (the Drosophila ortholog of human YAP/TAZ) via an evolutionarily conserved mechanism. Oncogenic signaling by the YAP/TAZ pathway occurs in cells that acquire CD109 expression in response to the inflammatory environment induced by radiation in clinically relevant models. Further, downregulation of Tep1 caused a reduction in Yki activity and reduced glioma growth. A key function of Yki in larval CNS is stem cell renewal and formation of neuroblasts. Other reports suggest different upstream regulators of Yki activity in the optic lobe versus the central brain regions of the larval CNS. We hypothesized that Tep1 interacts with the Hippo pathway effector Yki to regulate neuroblast numbers. We tested if Tep1 acts through Yki to affect glioma growth, and if in normal cells Tep1 affects neuroblast number and proliferation. Our data suggests that Tep1 affects Yki mediated stem cell renewal in glioma, as reduction of Tep significantly decreases the number of neuroblasts in glioma. Thus, we identify Tep1-Yki interaction in the larval CNS that plays a key role in glioma growth and progression. Frontiers Media S.A. 2020-05-08 /pmc/articles/PMC7225285/ /pubmed/32457905 http://dx.doi.org/10.3389/fcell.2020.00306 Text en Copyright © 2020 Gangwani, Snigdha and Kango-Singh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Gangwani, Karishma
Snigdha, Kirti
Kango-Singh, Madhuri
Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title_full Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title_fullStr Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title_full_unstemmed Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title_short Tep1 Regulates Yki Activity in Neural Stem Cells in Drosophila Glioma Model
title_sort tep1 regulates yki activity in neural stem cells in drosophila glioma model
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225285/
https://www.ncbi.nlm.nih.gov/pubmed/32457905
http://dx.doi.org/10.3389/fcell.2020.00306
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