Nakatani Hajime, Araki Keijiro, Jin Toufeng, Kobayashi Michiya, Sugimoto Takeki, Akimori Toyokazu, Namikawa Tsutomu, Okamoto Ken, Nakano Takumi, Okabayashi Takehiro, Hokimoto Norihiro, Kitagawa Hiroyuki, Taguchi Takahiro
Department of Tumor Surgery, Kochi Medical School, Nankoku, Kochi 783-8505, Japan.
Int J Mol Med. 2006 May;17(5):893-7.
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.