Imatinib mesylate (Glivec) inhibits Schwann cell viability and reduces the size of human plexiform neurofibroma in a xenograft model

Plexiform neurofibromas (PNF), one of the major features of neurofibromatosis type 1 (NF1), are characterized by complex cellular composition and mostly slow but variable growth patterns. In this study, we examined the effect of imatinib mesylate, a receptor tyrosine kinase inhibitor, on PNF-derived...

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Hauptverfasser: Demestre, Maria (VerfasserIn) , Herzberg, Jan (VerfasserIn) , Holtkamp, Nikola (VerfasserIn) , Hagel, Christian (VerfasserIn) , Reuss, David (VerfasserIn) , Friedrich, Reinhard E. (VerfasserIn) , Kluwe, Lan (VerfasserIn) , Deimling, Andreas von (VerfasserIn) , Mautner, Victor Felix (VerfasserIn) , Kurtz, Andreas (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2010
In: Journal of neuro-oncology
Year: 2010, Jahrgang: 98, Heft: 1, Pages: 11-19
ISSN:1573-7373
DOI:10.1007/s11060-009-0049-4
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s11060-009-0049-4
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Verfasserangaben:Maria Demestre, Jan Herzberg, Nikola Holtkamp, Christian Hagel, David Reuss, Reinhard E. Friedrich, Lan Kluwe, Andreas von Deimling, Victor-F. Mautner, Andreas Kurtz

MARC

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245 1 0 |a Imatinib mesylate (Glivec) inhibits Schwann cell viability and reduces the size of human plexiform neurofibroma in a xenograft model  |c Maria Demestre, Jan Herzberg, Nikola Holtkamp, Christian Hagel, David Reuss, Reinhard E. Friedrich, Lan Kluwe, Andreas von Deimling, Victor-F. Mautner, Andreas Kurtz 
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520 |a Plexiform neurofibromas (PNF), one of the major features of neurofibromatosis type 1 (NF1), are characterized by complex cellular composition and mostly slow but variable growth patterns. In this study, we examined the effect of imatinib mesylate, a receptor tyrosine kinase inhibitor, on PNF-derived Schwann cells and PNF tumour growth in vitro and in vivo. In vitro, PNF-derived primary Schwann cells express platelet-derived growth factors receptors (PDGFR) alpha and beta, both targets of imatinib, and cell viability was reduced by imatinib mesylate, with 50% inhibition concentration (IC(50)) of 10 microM. For in vivo studies, PNF tumour fragments xenografted onto the sciatic nerve of athymic nude mice were first characterized. The tumours persisted for at least 63 days and maintained typical characteristics of PNFs such as complex cellular composition, low proliferation rate and angiogenesis. A transient enlargement of the graft size was due to inflammation by host cells. Treatment with imatinib mesylate at a daily dose of 75 mg/kg for 4 weeks reduced the graft size by an average of 80% (n = 8), significantly different from the original sizes within the group and from sizes of the grafts in 11 untreated mice in the control group (P < 0.001). We demonstrated that grafting human PNF tumour fragments into nude mice provides an adequate in vivo model for drug testing. Our results provide in vivo and in vitro evidence for efficacy of imatinib mesylate for PNF. 
650 4 |a Adolescent 
650 4 |a Adult 
650 4 |a Animals 
650 4 |a Benzamides 
650 4 |a Brain Neoplasms 
650 4 |a Cell Line, Tumor 
650 4 |a Cell Size 
650 4 |a Cell Survival 
650 4 |a Disease Models, Animal 
650 4 |a Dose-Response Relationship, Drug 
650 4 |a Female 
650 4 |a Gene Expression Regulation, Neoplastic 
650 4 |a Humans 
650 4 |a Imatinib Mesylate 
650 4 |a Ki-67 Antigen 
650 4 |a Male 
650 4 |a Mice 
650 4 |a Mice, Inbred BALB C 
650 4 |a Mice, Nude 
650 4 |a Middle Aged 
650 4 |a Neoplasm Transplantation 
650 4 |a Neurofibroma, Plexiform 
650 4 |a Piperazines 
650 4 |a Protein Kinase Inhibitors 
650 4 |a Pyrimidines 
650 4 |a Receptor, Platelet-Derived Growth Factor alpha 
650 4 |a Receptor, Platelet-Derived Growth Factor beta 
650 4 |a S100 Proteins 
650 4 |a Schwann Cells 
650 4 |a Young Adult 
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