Vlaeminck M N, Collyn-d'Hooghe M, Cappelaere P, Biserte G, Oiry J, Montero J L, Imbach J L
Biomedicine. 1981 Mar;35(1):27-9.
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.
通过流式细胞荧光分析检测发现,EMT 6肿瘤细胞在与四种新型亚硝基脲衍生物:RPCNU、RFCNU、氯脲霉素(CZT)或185(CNCC)进行一小时体外孵育后,其DNA分布受到高度干扰。在用氯脲霉素(20微克/毫升)和CNCC(50微克/毫升)处理后,大多数细胞处于G2 + M期,并且这种积累持续超过48小时,在72小时之前没有任何恢复。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小时后恢复正常状态。这些细胞通过S期的进展速率降低以及在接触新化合物后观察到的G2期阻滞,应部分解释它们的抗肿瘤活性。