新型亚硝基脲衍生物对emt6肿瘤细胞“体外”增殖影响的流式细胞荧光分析。

M N Vlaeminck, M Collyn-d'Hooghe, P Cappelaere, G Biserte, J Oiry, J L Montero, J L Imbach
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引用次数: 0

摘要

流式细胞荧光分析显示,RPCNU、RFCNU、氯佐菌素(CZT)和185 (CNCC) 4种新型亚硝基脲衍生物体外培养1小时后,emt6肿瘤细胞的DNA分布受到高度干扰。氯佐菌素(20微克/毫升)和CNCC(50微克/毫升)处理后,大部分细胞处于G2 + M期,这种积累持续48小时以上,72小时前没有恢复。RPCNU(20微克/毫升)和RFCNU(50和65微克/毫升)在24小时内诱导细胞在G2 + M期积累。48小时后恢复正常。暴露于新化合物后,观察到细胞通过S期和G2阻滞的进展速度降低,这应该部分解释了它们的抗肿瘤活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Flow cytofluorometric analysis of the effects of new nitrosourea derivatives on proliferation of EMT 6 tumor cells "in vitro".

Examined by flow cytofluorometric analysis, the DNA distribution of EMT 6 tumor cells was highly perturbed after one hour of in vitro incubation with: RPCNU, RFCNU, chlorozotocin (CZT) or 185 (CNCC), four new nitrosourea derivatives. After the treatment with chlorozotocin (20 micrograms/ml) and CNCC (50 micrograms/ml), most of cells were in G2 + M phase and this accumulation lasted more than 48 hours without any restoration before 72 hours. RPCNU (20 micrograms/ml) and RFCNU (50 and 65 micrograms/ml) induced and accumulation of cells in G2 + M phase during 24 hours. The normal state was regained after 48 hours. These reduced rate of progression of the cells through S phase and the G2 block observed after exposure to the new compounds, should, in part, explain their antitumoral activity.

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