Ohyama S, Yonemura Y, Tugawa K, Kimura H, Kosaka T, Miyazaki I, Endo Y, Tanaka M, Sasaki T
Second Dept. of Surgery, School of Medicine, Kanazawa University, Japan.
Gan To Kagaku Ryoho. 1991 Jul;18(8):1273-8.
For the elucidation of the mode of action of anti-tumor agents, the cell cycle analysis of etoposide and podophyllotoxin was examined by means of the multiparameter flow cytometry using an anti-p-105 monoclonal antibody. The p-105 is one of the proliferation associated nuclear antigens and its expression increases with a cell cycle progression, especially in mitotic phase. Thus, we have applied its anti-monoclonal antibody to the discrimination between M and G2 phases of the gastric cancer cells. The results revealed that etoposide caused a G2 block and retarded an S phase transition, and podophyllotoxin caused both G2 and M phase blocks in the gastric cancer cells. This cell cycle analysis using an anti-p-105 monoclonal antibody would be a useful analysis of the antitumor agents, especially for M phase analysis of human cancer cells because of its rapidity and convenience.
为阐明抗肿瘤药物的作用方式,使用抗p - 105单克隆抗体,通过多参数流式细胞术对依托泊苷和鬼臼毒素进行细胞周期分析。p - 105是一种与增殖相关的核抗原,其表达随细胞周期进程增加,尤其在有丝分裂期。因此,我们将其抗单克隆抗体应用于胃癌细胞M期和G2期的区分。结果显示,依托泊苷导致G2期阻滞并延迟S期转换,鬼臼毒素在胃癌细胞中导致G2期和M期阻滞。这种使用抗p - 105单克隆抗体的细胞周期分析对于抗肿瘤药物将是一种有用的分析方法,特别是因其快速性和便利性,对于人类癌细胞的M期分析尤为如此。