Author/Authors :
Kondoh، نويسنده , , Masuo and Usui، نويسنده , , Takeo and Kobayashi، نويسنده , , Shinichi and Tsuchiya، نويسنده , , Kouichi and Nishikawa، نويسنده , , Kiyohiro and Nishikiori، نويسنده , , Takaaki and Mayumi، نويسنده , , Tadanori and Osada، نويسنده , , Hiroyuki، نويسنده ,
Abstract :
The biological effects of pironetin and its derivatives on cell cycle progression and antitumor activity were studied. At 10–20 ng/ml, both pironetin and its demethyl derivative, NK10958P completely inhibited the cell proliferation of 3Y1 cells, however, epoxypironetin showed only a weak inhibitory activity. The cell cycle analysis revealed that these compounds arrested the cell cycle progression at the M-phase in a dose-dependent manner. These antiproliferative effects of pironetin were also observed in the range 5–25 ng/ml with several tumor cell lines. In CDF1-SLC mice bearing P388 leukemia cells, the intraperitoneal administration of 6.3 mg/kg pironetin over a 5-day period showed a moderate antitumor effect (T/C, 128%). As the chemical structure of pironetin is different from other M-phase inhibitors such as colchicine or vinblastine, pironetin will be the lead compound for a potential new antitumor drug.