Hasegawa N, Kawamoto K, Uemura T
Department of Agriculture, Osaka Prefectural University.
Hum Cell. 1992 Jun;5(2):167-73.
An investigation was carried out to elucidate the mechanism of action of the oral antitumor agent 1-hexylcarbamoyl-5-fluorouracil (HCFU) by determining its effects on the growth and cell cycle of epipharyngeal carcinoma cells (KB cell) by DNA/BrdU double staining using flow cytometry (FCM). As a result, it was found that HCFU stimulates KB cells in the S phase to proliferate for the first 3 days of treatment in a low concentration (8 micrograms/ml) and caused cell accumulation in the later G2M phase. On the other hand, when administered in the concentration (20 micrograms/ml) that produces a 50 per cent cell kill, as determined from the cell growth curve, HCFU appeared to exhibit a cytocidal effect by blocking cells in S and G2M for the first 3 days after exposure. It was revealed by FCM for the first time that HCFU operates by a similar mechanism to that of 5-FU. This method seems to be of significance to therapeutic schemes that take into consideration the mechanism of action of antitumor drugs.
通过使用流式细胞术(FCM)进行DNA/BrdU双重染色,测定口服抗肿瘤药物1-己基氨基甲酰基-5-氟尿嘧啶(HCFU)对咽癌细胞(KB细胞)生长和细胞周期的影响,以阐明其作用机制。结果发现,低浓度(8微克/毫升)的HCFU在治疗的前3天刺激处于S期的KB细胞增殖,并导致细胞在随后的G2M期积累。另一方面,根据细胞生长曲线确定,当以产生50%细胞杀伤的浓度(20微克/毫升)给药时,HCFU在暴露后的前3天通过将细胞阻滞在S期和G2M期而表现出杀细胞作用。FCM首次揭示HCFU的作用机制与5-氟尿嘧啶相似。这种方法对于考虑抗肿瘤药物作用机制的治疗方案似乎具有重要意义。