Meyne J, Lockhart L H
Mutat Res. 1978 Sep;58(1):87-97. doi: 10.1016/0165-1218(78)90098-8.
Human lymphocytes were treated with the antitumor agent cis-platinum)II)diamminedichloride (PDD) during either the last 24 h or 48 h of incubation. A dose-dependent effect was observed for both inhibition of mitotic activity and increased frequency of metaphases with chromosomal aberrations. The aberrations observed consisted primarily of chromatid breaks. Statistical analysis of 3244 PDD-induced breakpoints demonstrated a significantly nonrandom distribution of breakpoints between chromosomes. The pattern of distribution varied with the type of aberration. Only chromosome number 9 had a significant increase of breakpoints for each type of aberration analyzed. The breakpoints were located predominantly in lightly staining G-gands. Certain individual bands had relatively high frequencies of breakpoints, indicating a specific interaciton occurs between PDD and the DNA of human lymphocytes in vitro.
在培养的最后24小时或48小时内,用抗肿瘤药物顺式二氯二氨合铂(II)(PDD)处理人淋巴细胞。观察到有丝分裂活性受到抑制以及中期出现染色体畸变的频率增加,均呈剂量依赖性效应。观察到的畸变主要是染色单体断裂。对3244个PDD诱导的断裂点进行统计分析表明,染色体之间的断裂点分布明显非随机。分布模式随畸变类型而变化。在所分析的每种畸变类型中,只有9号染色体的断裂点有显著增加。断裂点主要位于浅染的G带。某些个别条带的断裂点频率相对较高,表明在体外PDD与人淋巴细胞的DNA之间发生了特异性相互作用。