Trams G, v Urban M
Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1977 Aug 15;89(3):321-30. doi: 10.1007/BF00283786.
Steroidal alkylating agents are supposed to bind to steroid hormone receptors in target tissues. By this interaction the steroid portion might act as a carrier for the alkylating group. Three steroidal agents (phenesterin, estradiol mustard, dehydroepiandrosterone mustard) were tested for their capacity to combine with estrogen and androgen receptors in normal and malignant target tissues. For measuring steroid receptor complexes ager gel electrophoresis was used. All three compounds (added at a 10(3)-fold excess) revealed in vitro no competition to receptor sites (estrogen and androgen binding). After preincubation of intact tissue estrogen mustard was effective in inhibiting the binding of 3H-estradiol and dehydroepiandrosterone mustard reduced the uptake of 3H-5alpha-DHT. This may be due to liberating of estradiol and dehydroepiandrosterone, respectively, from the intact molecule. From these data it is unlikely that the cytostatic steroidal agents are more effective than other alkylating drugs.
甾体烷化剂被认为可与靶组织中的甾体激素受体结合。通过这种相互作用,甾体部分可能作为烷化基团的载体。测试了三种甾体药物(苯酯磷、雌二醇氮芥、脱氢表雄酮氮芥)在正常和恶性靶组织中与雌激素和雄激素受体结合的能力。使用琼脂凝胶电泳来测定甾体受体复合物。所有三种化合物(以10³倍过量添加)在体外均未显示出与受体位点(雌激素和雄激素结合)的竞争。完整组织预孵育后,雌二醇氮芥可有效抑制³H-雌二醇的结合,脱氢表雄酮氮芥可减少³H-5α-双氢睾酮的摄取。这可能分别是由于从完整分子中释放出了雌二醇和脱氢表雄酮。从这些数据来看,细胞抑制性甾体药物不太可能比其他烷化药物更有效。