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Evaluation of the Cytotoxicity of Cationic Polymers on Glioblastoma Cancer Stem Cells.
McCartin, Conor; Blumberger, Juliette; Dussouillez, Candice; Fernandez de Larrinoa, Patricia; Dontenwill, Monique; Herold-Mende, Christel; Lavalle, Philippe; Heurtault, Béatrice; Bellemin-Laponnaz, Stéphane; Fournel, Sylvie; Kichler, Antoine.
Afiliación
  • McCartin C; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
  • Blumberger J; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
  • Dussouillez C; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
  • Fernandez de Larrinoa P; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
  • Dontenwill M; Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) UMR7504, Université de Strasbourg & CNRS 23 rue du Loess, F-67083 Strasbourg, France.
  • Herold-Mende C; Laboratoire de Bioimagerie et Pathologies UMR CNRS 7021 (LBP), Faculté de Pharmacie, 74 route du Rhin, F-67401 Illkirch, France.
  • Lavalle P; Division of Neurosurgical Research, Department of Neurosurgery, University of Heidelberg, 69120 Heidelberg, Germany.
  • Heurtault B; Institut National de la Santé et de la Recherche Médicale, Inserm UMR_S 1121 Biomaterials and Bioengineering, F-67085 Strasbourg, France.
  • Bellemin-Laponnaz S; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
  • Fournel S; Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) UMR7504, Université de Strasbourg & CNRS 23 rue du Loess, F-67083 Strasbourg, France.
  • Kichler A; 3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
J Funct Biomater ; 14(1)2022 Dec 28.
Article en En | MEDLINE | ID: mdl-36662064
Cationic polymers such as polyethylenimine (PEI) have found a pervasive place in laboratories across the world as gene delivery agents. However, their applications are not limited to this role, having found a place as delivery agents for drugs, in complexes known as polymer-drug conjugates (PDCs). Yet a potentially underexplored domain of research is in their inherent potential as anti-cancer therapeutic agents, which has been indicated by several studies. Even more interesting is the recent observation that certain polycations may present a significantly greater toxicity towards the clinically important cancer stem cell (CSC) niche than towards more differentiated bulk tumour cells. These cells, which possess the stem-like characteristics of self-renewal and differentiation, are highly implicated in cancer drug resistance, tumour recurrence and poor clinical prognosis. The search for compounds which may target and eliminate these cells is thus of great research interest. As such, the observation in our previous study on a PEI-based PDC which showed a considerably higher toxicity of PEI towards glioblastoma CSCs (GSCs) than on more differentiated glioma (U87) cells led us to investigate other cationic polymers for a similar effect. The evaluation of the toxicity of a range of different types of polycations, and an investigation into the potential source of GSC's sensitivity to such compounds is thus described.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Funct Biomater Año: 2022 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Funct Biomater Año: 2022 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Suiza