Manni A, Pontari M, Wright C
Endocrinology. 1985 Nov;117(5):2040-3. doi: 10.1210/endo-117-5-2040.
Evidence obtained in human breast cancer cell lines in culture suggests that estradiol stimulates the synthesis of secretory proteins which may, in turn, mediate its mitogenic effect. We questioned whether a similar mechanism could mediate the growth-promoting effect of PRL in the N-nitrosomethylurea-induced rat mammary tumor grown in soft agar, where PRL exerts a dose-dependent colony-stimulating effect. Conditioned medium obtained from PRL-treated tumors, but not from control tumors, was found to exert a significant dose-dependent colony-stimulating effect when added to N-nitrosomethylurea-induced mammary tumors plated in soft agar under serum-free medium conditions. The growth-promoting action of conditioned medium from PRL-treated tumors was abolished by pretreatment with heat, trypsin, and Concanavalin-A, suggesting the possible glycoprotein nature of the oPRL-induced growth factor(s). These results provide support for the novel hypothesis that estradiol and PRL may support the growth of hormone-responsive breast cancer through a similar mechanism.
在培养的人乳腺癌细胞系中获得的证据表明,雌二醇刺激分泌蛋白的合成,而这些分泌蛋白反过来可能介导其促有丝分裂作用。我们质疑在软琼脂中生长的N-亚硝基甲基脲诱导的大鼠乳腺肿瘤中,类似的机制是否可以介导催乳素的促生长作用,在该肿瘤中催乳素发挥剂量依赖性的集落刺激效应。发现从经催乳素处理的肿瘤获得的条件培养基,而不是对照肿瘤的条件培养基,在无血清培养基条件下添加到接种在软琼脂中的N-亚硝基甲基脲诱导的乳腺肿瘤时,会产生显著的剂量依赖性集落刺激效应。经催乳素处理的肿瘤的条件培养基的促生长作用在经过热、胰蛋白酶和伴刀豆球蛋白A预处理后被消除,提示oPRL诱导的生长因子可能具有糖蛋白性质。这些结果为雌二醇和催乳素可能通过类似机制支持激素反应性乳腺癌生长这一新假说提供了支持。