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Glioblastoma cell migration is directed by electrical signals.
Clancy, Hannah; Pruski, Michal; Lang, Bing; Ching, Jared; McCaig, Colin D.
Afiliación
  • Clancy H; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
  • Pruski M; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom; School of Medicine, Tongji University, Shanghai, China.
  • Lang B; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
  • Ching J; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom; John Van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom. Electronic address: jared.ching@nhs.net.
  • McCaig CD; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom. Electronic address: c.mccaig@abdn.ac.uk.
Exp Cell Res ; 406(1): 112736, 2021 09 01.
Article en En | MEDLINE | ID: mdl-34273404
ABSTRACT
Electric field (EF) directed cell migration (electrotaxis) is known to occur in glioblastoma multiforme (GBM) and neural stem cells, with key signalling pathways frequently dysregulated in GBM. One such pathway is EGFR/PI3K/Akt, which is down-regulated by peroxisome proliferator activated receptor gamma (PPARγ) agonists. We investigated the effect of electric fields on primary differentiated and glioma stem cell (GSCs) migration, finding opposing preferences for anodal and cathodal migration, respectively. We next sought to determine whether chemically disrupting Akt through PTEN upregulation with the PPARγ agonist, pioglitazone, would modulate electrotaxis of these cells. We found that directed cell migration was significantly inhibited with the addition of pioglitazone in both differentiated GBM and GSCs subtypes. Western blot analysis did not demonstrate any change in PPARγ expression with and without exposure to EF. In summary we demonstrate opposing EF responses in primary GBM differentiated cells and GSCs can be inhibited chemically by pioglitazone, implicating GBM EF modulation as a potential target in preventing tumour recurrence.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Movimiento Celular / Neuroglía / PPAR gamma / Taxia Límite: Humans Idioma: En Revista: Exp Cell Res Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Movimiento Celular / Neuroglía / PPAR gamma / Taxia Límite: Humans Idioma: En Revista: Exp Cell Res Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido
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