Adams E F, Newton C J, Tait G H, Braunsberg H, Reed M J, James V H
Department of Chemical Pathology, St. Mary's Hospital Medical School, London, UK.
Int J Cancer. 1988 Jul 15;42(1):119-22. doi: 10.1002/ijc.2910420122.
We have previously shown that a stroma-associated paracrine influence may occur in the human breast. In particular, human breast fibroblasts secrete a factor which stimulates reductive 17 beta-oestradiol dehydrogenase (HSD) activity, thereby regulating tissue concentrations of 17 beta-oestradiol. We report here the results of experiments designed to establish the nature of the enzyme activity stimulating factor. In vitro cell culture techniques were used, in which human breast fibroblast-conditioned medium was used to grow the human breast cancer cell line, MCF-7, for 6 days, after which the reductive HSD activity of the monolayers was assessed. The fibroblastic reductive HSD stimulating factor was found to be a trypsin-sensitive polypeptide. The polypeptide eluted from a Sephadex G-75 column as a peak corresponding to a molecular weight of about 50 kDa. The polypeptide exerts its effects by altering the Vmax of 2 of the cytosolic forms of HSD within MCF-7 cells. This is achieved by a protein-synthesis-dependent but calmodulin-independent mechanism. These results provide further evidence of a paracrine effect by stromal tissue within the human breast and have important implications with respect to the aetiology and treatment of breast cancer.
我们之前已经表明,人乳腺中可能存在一种与基质相关的旁分泌影响。具体而言,人乳腺成纤维细胞分泌一种因子,该因子可刺激还原型17β-雌二醇脱氢酶(HSD)的活性,从而调节组织中17β-雌二醇的浓度。我们在此报告旨在确定这种酶活性刺激因子性质的实验结果。采用体外细胞培养技术,用人乳腺成纤维细胞条件培养基培养人乳腺癌细胞系MCF-7 6天,之后评估单层细胞的还原型HSD活性。发现成纤维细胞还原型HSD刺激因子是一种对胰蛋白酶敏感的多肽。该多肽从Sephadex G-75柱上洗脱下来时呈现出一个对应分子量约为50 kDa的峰。该多肽通过改变MCF-7细胞内两种胞质形式HSD的Vmax发挥作用。这是通过一种依赖蛋白质合成但不依赖钙调蛋白的机制实现的。这些结果为人类乳腺中基质组织的旁分泌作用提供了进一步证据,并且对乳腺癌的病因学和治疗具有重要意义。