Ikegami Y, Yano S, Nakao K
Drug Discovery Research Unit, Ciba-Geigy Japan Ltd., Takarazuka.
Arzneimittelforschung. 1996 Feb;46(2):201-4.
CGP 41251 (4'-N-benzoyl staurosporine, CAS 120685-11-2) exerts increased selectivity for Ca(2+)- and phospholipid-dependent protein kinase C inhibition. In this study, the effects of CGP 41251 on cell cycle distribution and growth inhibition were examined in SBC3 human small cell lung cancer (SCLC) cell line. CGP 41251 caused the inhibition of cell proliferation and at 1.0 mumol/l showed almost complete effect. In early S phase synchronized SBC3 cells, CGP 41251 at 1.0 mumol/l did not inhibit an initial progression from early S to G2 phase, but it blocked a process from G2/M to G1 phase completely. After removal of nocodazole block, CGP 41251 at 1.0 mumol/l caused DNA re-replication and induction of polyploidy. In nude mice xenograft, CGP 41251 at a dose of 200 mg/kg showed statistically significant inhibition against this tumor with a T/C value of 21.4%. Histopathologically, expansion of central necrosis was observed by the administration of CGP 41251. These results in SBC3 cells indicated that CGP 41251 showed antitumor activity through the inhibition of cell cycle progression from G2/M to G1 phase, and through induction of cells with higher DNA content.
CGP 41251(4'-N-苯甲酰基星形孢菌素,CAS 120685-11-2)对钙和磷脂依赖性蛋白激酶C的抑制作用具有更高的选择性。在本研究中,检测了CGP 41251对SBC3人小细胞肺癌(SCLC)细胞系细胞周期分布和生长抑制的影响。CGP 41251导致细胞增殖受到抑制,在1.0 μmol/L时显示出几乎完全的抑制效果。在早期S期同步化的SBC3细胞中,1.0 μmol/L的CGP 41251并不抑制从早期S期到G2期的初始进程,但它完全阻断了从G2/M期到G1期的进程。去除诺考达唑阻滞作用后,1.0 μmol/L的CGP 41251导致DNA重新复制并诱导多倍体形成。在裸鼠异种移植模型中,200 mg/kg剂量的CGP 41251对该肿瘤显示出统计学上显著的抑制作用,T/C值为21.4%。组织病理学检查显示,给予CGP 41251后观察到中央坏死扩大。SBC3细胞中的这些结果表明,CGP 41251通过抑制从G2/M期到G1期的细胞周期进程以及诱导具有更高DNA含量的细胞而表现出抗肿瘤活性。