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3'-叠氮-3'-脱氧胸苷对HL60细胞周期的急性影响。

Acute effects of 3'-azido-3'-deoxythymidine on the cell cycle of HL60 cells.

作者信息

Roskrow M, Wickramasinghe S N

机构信息

Department of Haematology, St Mary's Hospital Medical School, Imperial College, University of London, Norfolk Place, UK.

出版信息

Clin Lab Haematol. 1990;12(2):177-84.

PMID:2208948
Abstract

The average doubling times of HL60 cells grown in the presence of 0,5,10 and 100 microM 3'-azido-3'-deoxythymidine (AZT) for 72 h were, respectively, 51.1, 65.7, 69.0 and 76.3 h. This drug-concentration-dependent prolongation of the cell-doubling time was associated with a progressive increase in modal cell volume. The technique of combined Feulgen microspectrophotometry and 3H-thymidine autoradiography revealed that the cell cycle distribution of HL60 cells cultured in the presence of 5 and 100 microM AZT for 48 h was abnormal, with an increased percentage of cells in the S phase and a decreased percentage in the G1phase. From the cell doubling times and the cell cycle distribution data, and making a number of assumptions, upper limit estimates for the duration of the S phase in cultures containing 0,5 and 100 microM AZT were calculated to be 26.2, 35.8 and 49.6 h, respectively. The data indicate that concentrations of AZT achieved in the plasma of patients receiving this drug (i.e. 5 microM) cause a substantial prolongation of both the cell cycle time and the duration of the S phase of HL60 cells. It therefore seems likely that some of the toxic effects of AZT seen in vivo, including impairment of bone marrow function, are at least partly related to AZT-induced disturbances of DNA synthesis and proliferation in human cells.

摘要

在分别含有0、5、10和100微摩尔3'-叠氮-3'-脱氧胸苷(AZT)的条件下培养72小时的HL60细胞,其平均倍增时间分别为51.1、65.7、69.0和76.3小时。这种细胞倍增时间的药物浓度依赖性延长与细胞模态体积的逐渐增加相关。Feulgen显微分光光度法与³H-胸腺嘧啶核苷放射自显影相结合的技术显示,在含有5和100微摩尔AZT的条件下培养48小时的HL60细胞的细胞周期分布异常,S期细胞百分比增加,G1期细胞百分比减少。根据细胞倍增时间和细胞周期分布数据,并做出一些假设,计算出在含有0、5和100微摩尔AZT的培养物中S期持续时间的上限估计值分别为26.2、35.8和49.6小时。这些数据表明,接受该药物治疗的患者血浆中达到的AZT浓度(即5微摩尔)会导致HL60细胞的细胞周期时间和S期持续时间大幅延长。因此,体内观察到的AZT的一些毒性作用,包括骨髓功能损害,似乎至少部分与AZT诱导的人体细胞DNA合成和增殖紊乱有关。

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