Murakami M, Fukami J
Arch Toxicol. 1983 Jul;53(3):245-8. doi: 10.1007/BF00316508.
The binding of 3H-labeled steroid hormones and a non-steroidal synthetic estrogen, diethylstilbestrol (DES), to proteins of cultured human embryonic lung cells (HEL 299) was studied according to the methods of Diamond et al. [Cancer Res 27: 890-897 (1967)] and Kuroki and Heidelberger [Cancer Res 31: 2168-2176 (1971)]. Ecdysone, estradiol, hydrocortisone, progesterone, testosterone, and DES were selected as test compounds. The aim of this study was to determine the protein binding ability of DES, known as a transplacental carcinogen and teratogen for humans, and to compare it with those of the steroid hormones. DES was bound to proteins to the highest extent, and the amount of binding of estradiol was slightly lower than that of DES. Hydrocortisone, testosterone, and progesterone bound to proteins to smaller extents than DES and estradiol. Very little binding of ecdysone to cellular proteins was detected.
根据戴蒙德等人[《癌症研究》27: 890 - 897(1967)]以及黑木和海德堡格[《癌症研究》31: 2168 - 2176(1971)]的方法,研究了3H标记的甾体激素和一种非甾体合成雌激素己烯雌酚(DES)与培养的人胚肺细胞(HEL 299)蛋白质的结合情况。选择蜕皮激素、雌二醇、氢化可的松、孕酮、睾酮和DES作为测试化合物。本研究的目的是确定已知对人类具有经胎盘致癌和致畸作用的DES的蛋白质结合能力,并将其与甾体激素的蛋白质结合能力进行比较。DES与蛋白质的结合程度最高,雌二醇的结合量略低于DES。氢化可的松、睾酮和孕酮与蛋白质的结合程度低于DES和雌二醇。未检测到蜕皮激素与细胞蛋白质的明显结合。