| Literature DB >> 16596277 |
Hajime Nakatani1, Keijiro Araki, Toufeng Jin, Michiya Kobayashi, Takeki Sugimoto, Toyokazu Akimori, Tsutomu Namikawa, Ken Okamoto, Takumi Nakano, Takehiro Okabayashi, Norihiro Hokimoto, Hiroyuki Kitagawa, Takahiro Taguchi.
Abstract
STI571 is a specific inhibitor of tyrosine kinases, such as BCR-ABL, platelet-derived growth factor receptor, and c-KIT, and has recently been approved for the treatment of chronic myeloid leukemia and gastrointestinal stromal tumors (GISTs). This study demonstrated that STI571 induces cell death in the gastrointestinal stromal tumor cell line, GIST-T1. In these cells, STI571 induced pro-caspase-12 or pro-caspase-7 cleavage and it affected caspase-3 activity and induced the endoplasmic reticulum (ER)-resident chaperone, glucose-regulated protein 78. The STI571-induced cell death was blocked by the protein synthesis inhibitor, cycloheximide. Together, these results suggest that STI571 induces cell death in GIST-T1 cells, at least in part, via the ER stress response.Entities:
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Year: 2006 PMID: 16596277
Source DB: PubMed Journal: Int J Mol Med ISSN: 1107-3756 Impact factor: 4.101