Honeycombe J R
Mutat Res. 1978 Mar;57(1):35-49. doi: 10.1016/0027-5107(78)90232-4.
In vitro exposure of human lymphocytes to busulphan (BUS) produced an increase in chromosome aberrations and in sister-chromatid exchange (SCE) frequency. The distribution of chromosome breaks throughout the karyotype was non-random and they occurred mainly in the G-negative bands. Certain bands had a marked susceptibility to BUS and comparisons with the human chromosome-break distributions reported for a number of drugs revealed that some of these bands were equally susceptible to other alkylating agents. Both the number of chromosome gaps and breaks and the SCE frequency increased with BUS concentration, but only the SCE dose--response was a clearly defined linear relationship. Therefore a standard SCE dose--response curve was constructed for future comparison with the results of similar investigations of patients on BUS therapy.
将人淋巴细胞在体外暴露于白消安(BUS),会导致染色体畸变和姐妹染色单体交换(SCE)频率增加。整个核型中染色体断裂的分布是非随机的,主要发生在G阴性带。某些带对白消安具有明显的易感性,与报道的多种药物所致人类染色体断裂分布进行比较发现,其中一些带对其他烷化剂同样易感。染色体间隙和断裂的数量以及SCE频率均随白消安浓度增加而增加,但只有SCE剂量-反应呈明确的线性关系。因此构建了标准的SCE剂量-反应曲线,以便将来与接受白消安治疗患者的类似研究结果进行比较。