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用5-氟尿嘧啶使L1210细胞部分同步化及其在药物联合中的应用。

Partial synchronization of L1210 cells by 5-fluorouracil and its use in drug combinations.

作者信息

Bhuyan B K, Blowers C L, Neil G L, Bono V H, Day K J

出版信息

Cancer Res. 1977 Sep;37(9):3204-8.

PMID:560250
Abstract

When L1210 cells growing logarithmically were exposed for 8 hr to a nonlethal dose of 5-fluorouracil (FU) (0.25 microgram/ml), the percentage of cells in S phase increased from 74.9% in the asynchronous culture to 93% in the FU-treated culture. This resulted in increased cell-kill by S-phase-specific inhibitors [1-beta-D-arabinofuranosylcytosine (ara-C), 5-hydroxy-2-formylpyridinethiosemicarbazone] when they were added to a culture partially synchronized by pretreatment with FU. For example, 2 hr exposure to ara-C alone or ara-C plus FU (added simultaneously to asynchronous culture) gave 28.8 and 25.8% survival, respectively, compared to 6.8% survival when ara-C was added for 2 hr to the partially synchronized culture. Eight to 12 hr after FU removal, the culture became asynchronous, such that ara-C addition at this time did not result in increased cell-kill. Cultures pretreated with FU were also highly sensitive to vincristine and Adriamycin. Adriamycin acted synergistically with FU (after 8 hr pretreatment) in killing L1210 cells.

摘要

当对数生长期的L1210细胞暴露于非致死剂量的5-氟尿嘧啶(FU)(0.25微克/毫升)8小时后,S期细胞的百分比从异步培养中的74.9%增加到FU处理培养中的93%。当将S期特异性抑制剂[1-β-D-阿拉伯呋喃糖基胞嘧啶(ara-C)、5-羟基-2-甲酰基吡啶硫代半卡巴腙]添加到通过FU预处理部分同步的培养物中时,这导致细胞杀伤增加。例如,单独暴露于ara-C 2小时或ara-C加FU(同时添加到异步培养物中)分别产生28.8%和25.8%的存活率,而将ara-C添加到部分同步培养物中2小时时存活率为6.8%。去除FU 8至12小时后,培养物变为异步,因此此时添加ara-C不会导致细胞杀伤增加。用FU预处理的培养物对长春新碱和阿霉素也高度敏感。阿霉素与FU(预处理8小时后)协同作用杀死L1210细胞。

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