Tselepi M R, Demopoulos N A, Catsoulacos P
Department of Biology, University of Patras, Greece.
Mutagenesis. 1989 Sep;4(5):361-4. doi: 10.1093/mutage/4.5.361.
3 beta-Hydroxy-13 alpha-amino-13,17-seco-5 alpha-androstan-17-oic-13,17-lactam-p-bis(2-chloroethyl) aminophenoxyacetate (NSC 294859) is a new modified steroidal alkylating agent. This compound was given by i.p. administration to mice bearing different types of tumour. It was found to exhibit good activity in L1210 and P388 leukaemias with maintenance of activity against advanced tumours. The treatment of colon 26 tumour and B16 melanoma resulted in positive antineoplastic activity. The drug was not shown to be active in a melphalan-resistant P388 line. In this study, NSC 294859 was found to be effective in causing statistically significant increases in sister-chromatid exchange (SCE) rates and cell division delays. The alkylating agent component, p-bis-(2-chloroethyl)aminophenoxy acetic acid, was shown to be less effective than the parent compound, while the modified steroid component, 3 beta-hydroxy-13 alpha-amino-13,17-seco-5 alpha-androstan-17-oic-13,17-lactam, showed no effect. There were no statistically significant differences among donors regarding the induction of SCEs and replication indices (RIs) for the compounds tested.
3β-羟基-13α-氨基-13,17-开环-5α-雄甾烷-17-酸-13,17-内酰胺-对-双(2-氯乙基)氨基苯氧乙酸酯(NSC 294859)是一种新型的改性甾体烷化剂。该化合物经腹腔注射给予患有不同类型肿瘤的小鼠。结果发现它在L1210和P388白血病中表现出良好的活性,对晚期肿瘤也保持活性。对结肠26肿瘤和B16黑色素瘤的治疗产生了积极的抗肿瘤活性。该药物在耐美法仑的P388细胞系中未显示出活性。在本研究中,发现NSC 294859能有效导致姐妹染色单体交换(SCE)率和细胞分裂延迟出现统计学上的显著增加。烷化剂成分对-双(2-氯乙基)氨基苯氧乙酸的效果不如母体化合物,而改性甾体成分3β-羟基-13α-氨基-13,17-开环-5α-雄甾烷-17-酸-13,17-内酰胺则无效果。在供体之间,所测试化合物诱导SCE和复制指数(RI)方面没有统计学上的显著差异。