Establishment and Characterization of a Human Gastrointestinal Stromal Tumour (GIST) Xenograft in Athymic Nude Mice

Background: The majority of gastrointestinal stromal tumours (GISTs) contain oncogenic KIT (v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog) or platelet-derived growth factor-alpha (PDGFRA) receptor tyrosine kinase (TK) mutations and are initially, but only temporarily sensitive to TK...

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Veröffentlicht in:Anticancer research 2009-11, Vol.29 (11), p.4331-4336
Hauptverfasser: Revheim, Mona-Elisabeth, Seierstad, Therese, Berner, Jeanne-Marie, Bruland, Oyvind Sverre, Røe, Kathrine, Ohnstad, Hege Oma, Bjerkehagen, Bodil, Bach-Gansmo, Tore
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Sprache:eng
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Zusammenfassung:Background: The majority of gastrointestinal stromal tumours (GISTs) contain oncogenic KIT (v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog) or platelet-derived growth factor-alpha (PDGFRA) receptor tyrosine kinase (TK) mutations and are initially, but only temporarily sensitive to TK inhibitors. The aim of this study was to establish and characterize a human GIST xenograft that could be used for evaluating various molecularly targeted therapies. Materials and Methods: GIST tissue from four patients was implanted under the skin of athymic nude mice. In one case a tumour line was established. Results: The xenograft showed characteristic GIST morphology and exhibited the same mutation profile as that of the patient. Conclusion: A human GIST xenograft with mutation in KIT exons 11 and 17 has been established and maintained in nude mice for 3 years (13 passages). This model will enable further studies on mechanisms of resistance, combination therapies and allow testing of novel targeted therapies.
ISSN:0250-7005
1791-7530