<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dufour C</submitter><funding>Association pour la Recherche sur le Cancer</funding><funding>Coordenação de Aperfeiçoamento do Pessoal de Nivel Superior-Comité Français d&amp;apos;Évaluation de la Coopération Universitaire et Scientifique avec le Brésil</funding><funding>Institut National de la Santé et de la Recherche Médicale</funding><funding>Fondation pour la Recherche Médicale</funding><funding>Association pour la Recherche dans les Tumeurs Cérébrales</funding><pagination>2373-82</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3245240</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(10)</volume><pubmed_abstract>Gliomas, the most frequent primitive central nervous system tumors, have been suggested to originate from astrocytes or from neural progenitors/stem cells. However, the precise identity of the cells at the origin of gliomas remains a matter of debate because no pre-neoplastic state has been yet identified. Transforming growth factor (TGF)-alpha, an epidermal growth factor family member, is frequently overexpressed in the early stages of glioma progression. We previously demonstrated that prolonged exposure of astrocytes to TGF-alpha is sufficient to trigger their reversion to a neural progenitor-like state. To determine whether TGF-alpha dedifferentiating effects are associated with cancerous transforming effects, we grafted intracerebrally dedifferentiated astrocytes. We show that these c</pubmed_abstract><journal>Stem cells (Dayton, Ohio)</journal><pubmed_title>Astrocytes reverted to a neural progenitor-like state with transforming growth factor alpha are sensitized to cancerous transformation.</pubmed_title><pmcid>PMC3245240</pmcid><funding_grant_id>3500</funding_grant_id><funding_grant_id>3972</funding_grant_id><funding_grant_id>3131</funding_grant_id><pubmed_authors>Daudigeos E</pubmed_authors><pubmed_authors>Sharif A</pubmed_authors><pubmed_authors>Dias-Morais A</pubmed_authors><pubmed_authors>Lazar V</pubmed_authors><pubmed_authors>Cadusseau J</pubmed_authors><pubmed_authors>Varlet P</pubmed_authors><pubmed_authors>Dufour C</pubmed_authors><pubmed_authors>de Faria GP</pubmed_authors><pubmed_authors>Leonard N</pubmed_authors><pubmed_authors>Dantas-Barbosa C</pubmed_authors><pubmed_authors>Grill J</pubmed_authors><pubmed_authors>Surena AL</pubmed_authors><pubmed_authors>Auger N</pubmed_authors><pubmed_authors>Chneiweiss H</pubmed_authors><pubmed_authors>Dessen P</pubmed_authors><pubmed_authors>Vassal G</pubmed_authors><pubmed_authors>Prevot V</pubmed_authors><pubmed_authors>Junier MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Astrocytes reverted to a neural progenitor-like state with transforming growth factor alpha are sensitized to cancerous transformation.</name><description>Gliomas, the most frequent primitive central nervous system tumors, have been suggested to originate from astrocytes or from neural progenitors/stem cells. However, the precise identity of the cells at the origin of gliomas remains a matter of debate because no pre-neoplastic state has been yet identified. Transforming growth factor (TGF)-alpha, an epidermal growth factor family member, is frequently overexpressed in the early stages of glioma progression. We previously demonstrated that prolonged exposure of astrocytes to TGF-alpha is sufficient to trigger their reversion to a neural progenitor-like state. To determine whether TGF-alpha dedifferentiating effects are associated with cancerous transforming effects, we grafted intracerebrally dedifferentiated astrocytes. We show that these c</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Oct</publication><modification>2026-05-01T02:04:08.941Z</modification><creation>2026-04-07T16:34:10.972Z</creation></dates><accession>S-EPMC3245240</accession><cross_references><pubmed>19544474</pubmed><doi>10.1002/stem.155</doi></cross_references></HashMap>