Sawecka J, Gołos B, Malec J
Department of Biochemistry, Institute of Hematology, Warsaw, Poland.
Neoplasma. 1987;34(4):369-77.
The effect of caffeine (CAF) on acute cytotoxic response of L5178Y lymphoblasts to hydroxyurea (HU) treatment was studied. The following events were examined: abnormal cell enlargement (giant cell formation), the rate of recovery of cell reproduction and DNA synthesis after releasing the cells from the HU blockage, parental DNA breakage and cell death. The presence of CAF at nontoxic concentration prevented giant cell formation, enhanced cell growth inhibition and cell killing. The effect of CAF was variable, dependent on the duration of exposure to HU and the time of exposure to CAF. To obtain maximal effect, the continuous presence of CAF during HU treatment and posttreatment time was necessary. Hydroxyapatite chromatography assay of single strand (ss) and double strand (ds) fractions in parental DNA and the measurement of the rate of post-treatment recovery of DNA synthesis indicated that CAF enhanced HU-induced DNA lesions. It is concluded that the results give further evidence that even short HU treatment can damage not only newly formed but also parental DNA. The lesions are normally, at least partly repaired and can be expressed under the conditions of DNA repair inhibition.
研究了咖啡因(CAF)对L5178Y淋巴母细胞对羟基脲(HU)处理的急性细胞毒性反应的影响。检测了以下事件:细胞异常增大(巨细胞形成)、细胞从HU阻滞中释放后细胞增殖和DNA合成的恢复率、亲本DNA断裂和细胞死亡。无毒浓度的CAF可防止巨细胞形成,增强细胞生长抑制和细胞杀伤作用。CAF的作用是可变的,取决于暴露于HU的持续时间和暴露于CAF的时间。为了获得最大效果,在HU处理和处理后期间持续存在CAF是必要的。对亲本DNA中单链(ss)和双链(ds)片段进行羟基磷灰石色谱分析以及对DNA合成后处理恢复率的测量表明,CAF增强了HU诱导的DNA损伤。得出的结论是,这些结果进一步证明,即使是短时间的HU处理不仅会损伤新形成的DNA,也会损伤亲本DNA。这些损伤通常至少会部分修复,并且在DNA修复抑制的条件下可能会表现出来。