Mistry D, Weaver J P, Riches A
Prostate. 1983;4(3):307-14. doi: 10.1002/pros.2990040310.
The proliferative responses of human prostatic carcinoma have been evaluated in organ culture using [125I]-iododeoxyuridine ([125I]UdR) to monitor DNA synthesis. The morphological preservation was not influenced by the addition of fetal calf serum or insulin (5 mu gm/ml), transferrin (10 mu gm/ml), and thyrotropin releasing hormone (10(-9) M) to the active medium. Testosterone (4 X 10(-7) M) stimulated [125I]UdR uptake, whereas diethylstilboestrol (4 X 10(-6) M) had no direct effect on uptake. Both estramustine phosphate (4 X 10(-6) M) and oestradiol-17 beta (4 X 10(-6) M) inhibited uptake in a similar manner. Thus while explants of human prostatic carcinoma derived from transurethrally resected specimens can be well maintained in organ culture for a few days, proliferative responses are small and difficult to measure for individual patients.
利用[125I] - 碘脱氧尿苷([125I]UdR)监测DNA合成,在器官培养中评估了人前列腺癌的增殖反应。向活性培养基中添加胎牛血清或胰岛素(5μg/ml)、转铁蛋白(10μg/ml)和促甲状腺激素释放激素(10^(-9)M),并不影响形态学保存。睾酮(4×10^(-7)M)刺激[125I]UdR摄取,而己烯雌酚(4×10^(-6)M)对摄取无直接影响。磷酸雌莫司汀(4×10^(-6)M)和雌二醇 - 17β(4×10^(-6)M)均以类似方式抑制摄取。因此,虽然经尿道切除标本来源的人前列腺癌外植体在器官培养中可良好维持数天,但个体患者的增殖反应较小且难以测量。