Kalweit S, Obe G
Mutat Res. 1984 Aug;128(1):59-64. doi: 10.1016/0027-5107(84)90047-2.
Liquid holding of trenimon-treated human peripheral lymphocytes in the G0 stage of the cell cycle leads to an elevation in the frequencies of chromosome aberrations and a decrease in the frequencies of chromatid aberrations. The frequencies of aberrant metaphases are not influenced significantly under these experimental conditions. Storage of trenimon-treated cells in the presence of 1-beta-D-arabinosylcytosine (araC) leads to an additional increase in the frequencies of chromosome-type aberrations, with an increase in the frequencies of aberrant metaphases as well. These findings are interpreted as DNA double-strand breaks being formed during the repair of damaged DNA, and that araC exaggerates this effect by inhibiting repair. AraC does not influence the frequencies of SCEs significantly, which indicates that either the lesions or the repair pathways leading to chromosome aberrations are different from those leading to SCEs.
将曲尼司特处理过的人外周血淋巴细胞保持在细胞周期的G0期,会导致染色体畸变频率升高,染色单体畸变频率降低。在这些实验条件下,异常中期的频率没有受到显著影响。在1-β-D-阿拉伯糖胞苷(araC)存在的情况下储存曲尼司特处理过的细胞,会导致染色体型畸变频率进一步增加,同时异常中期的频率也会增加。这些发现被解释为在受损DNA修复过程中形成了DNA双链断裂,而araC通过抑制修复夸大了这种效应。AraC对姐妹染色单体交换频率没有显著影响,这表明导致染色体畸变的损伤或修复途径与导致姐妹染色单体交换的不同。