Aitken S C, Lippman M E
Cancer Res. 1985 Apr;45(4):1611-20.
The effect of estrogens and antiestrogens is examined on three enzymes the activities of which are known to correlate with cell growth. Estrogen treatment increases thymidylate synthetase binding sites up to 4-fold over controls. The extent of induction is dependent on incubation time and the basal rate of cell growth in untreated cells. Amount of active enzyme generally shows a positive correlation with rates of DNA synthesis and cell growth. Thymidine kinase activity and the number of dihydrofolate reductase binding sites are similarly induced by estrogen treatment. Conversely, the effect of antiestrogens on MCF-7 cells is exceedingly complex in that responses in enzyme activities and several generally accepted indices of cell growth (cell number, protein content, rate of DNA synthesis) are dissimilar. Dose response, magnitude of response, and direction of response (increase or decrease) are distinct for each enzyme and for each measure of cell growth with each antiestrogen tested. These results suggest that specific cellular activities are modulated independently by estrogens and antiestrogens and that changes in ligand-receptor complex cannot be the sole explanation for the specificity of estrogen and antiestrogen action. Some degree of specificity and heterogeneity may reside at the level of receptor interaction with the various genes subject to estrogenic modulation.
研究了雌激素和抗雌激素对三种酶的作用,已知这三种酶的活性与细胞生长相关。雌激素处理使胸苷酸合成酶结合位点比对照增加高达4倍。诱导程度取决于孵育时间和未处理细胞中的基础细胞生长速率。活性酶的量通常与DNA合成速率和细胞生长速率呈正相关。雌激素处理同样诱导胸苷激酶活性和二氢叶酸还原酶结合位点的数量。相反,抗雌激素对MCF - 7细胞的作用极其复杂,因为酶活性的反应以及几种普遍接受的细胞生长指标(细胞数量、蛋白质含量、DNA合成速率)都不相同。对于每种酶以及每种抗雌激素测试的每种细胞生长测量指标,剂量反应、反应幅度和反应方向(增加或减少)都是不同的。这些结果表明,雌激素和抗雌激素独立调节特定的细胞活性,并且配体 - 受体复合物的变化不能作为雌激素和抗雌激素作用特异性的唯一解释。某种程度的特异性和异质性可能存在于受体与受雌激素调节的各种基因相互作用的水平。