Blankenstein M A, Henkelman M S, Klijn J G
Eur J Cancer Clin Oncol. 1985 Dec;21(12):1493-9. doi: 10.1016/0277-5379(85)90244-5.
The effect of the LHRH agonist Buserelin on the MCF-7 human breast cancer cell line was studied. Cells were cultured in medium containing 10% untreated foetal calf serum or 10% steroid-depleted serum. In both media the DNA and protein content of cultures kept for 3-5 days in the presence of 80-800 nM Buserelin and 1 nM oestradiol were 8-27% lower than those of flasks cultured in the presence of oestradiol alone (P less than 0.05). LHRH itself (400 nM) also displayed an antiproliferative effect on the MCF-7 cultures. At an equimolar concentration, the LHRH antagonist ORG 30093D abolished the antiproliferative effect of Buserelin. MCF-7 cells did not specifically take up radioiodinated LHRH. Our data are the first to indicate that LHRH analogues may inhibit the growth of MCF-7 cells to a limited extent. The antitumour activity of these compounds in vivo may, then, be due to the main pituitary and gonadal effects, resulting in a decrease of the concentration of oestrogen in the circulation and, in addition, a direct effect at the target cell level.
研究了促黄体生成素释放激素(LHRH)激动剂布舍瑞林对MCF - 7人乳腺癌细胞系的作用。细胞在含有10%未处理胎牛血清或10%类固醇去除血清的培养基中培养。在这两种培养基中,在80 - 800 nM布舍瑞林和1 nM雌二醇存在下培养3 - 5天的培养物的DNA和蛋白质含量比仅在雌二醇存在下培养的培养瓶低8 - 27%(P小于0.05)。LHRH本身(400 nM)对MCF - 7培养物也显示出抗增殖作用。在等摩尔浓度下,LHRH拮抗剂ORG 30093D消除了布舍瑞林的抗增殖作用。MCF - 7细胞不会特异性摄取放射性碘化LHRH。我们的数据首次表明LHRH类似物可能在一定程度上抑制MCF - 7细胞的生长。这些化合物在体内的抗肿瘤活性可能归因于主要的垂体和性腺作用,导致循环中雌激素浓度降低,此外,还归因于在靶细胞水平的直接作用。