Abstract
Background: The clinical outcome of gastrointestinal stromal tumor (GIST) has been improved by the introduction of molecular-targeting drugs. However, resistance to these drugs appears during the course of treatment. The aim of this study was to establish and characterize a human xenograft model of GIST. Materials and Methods: GIST tissue from a patient with esophageal GIST was implanted under the skin of a NOD-SCID mouse. The tumor became successfully engrafted and we investigated the effects of imatinib and sunitinib on this model. KIT mutation was investigated by complementary DNA analysis, and c-KIT (CD117) expression was evaluated by immunohistological staining. Results: cDNA analysis of the tumor revealed a KIT mutation in exon 11. c-KIT expression was observed in each passaged tumor. Both imatinib and sunitinib significantly reduced the size of the xenograft tumor. Conclusion: We established a novel xenograft model of human GIST in mice. This xenograft model may be useful for studying GIST.
Original language | English |
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Pages (from-to) | 175-182 |
Number of pages | 8 |
Journal | Anticancer Research |
Volume | 33 |
Issue number | 1 |
State | Published - 2013/01 |
Keywords
- Gastrointestinal stromal tumor
- Imatinib
- Mouse
- Sunitinib
- Xenograft
ASJC Scopus subject areas
- Oncology
- Cancer Research