Boccuzzi G, Brignardello E, Di Monaco M, Gatto V, Leonardi L, Pizzini A, Gallo M
Department of Clinical Pathophysiology, University of Turin, Italy.
Br J Cancer. 1994 Dec;70(6):1035-9. doi: 10.1038/bjc.1994.444.
Adrenal androgens show a dual and apparently opposite effect on the growth of oestrogen-responsive breast cancer: they stimulate growth on their own, but counteract the growth-stimulatory effect of oestrogens. Focusing on the inhibitory action we have studied the effects of 5-en-androstene-3 beta,17 beta-diol (ADIOL) on the growth of oestrogen-responsive MCF-7 breast cancer cells in the presence of oestrogens (oestradiol and diethylstilboestrol), antiestrogens (tamoxifen) and antiandrogens (hydroxyflutamide). The inhibition of oestrogen-stimulated growth, attained with nanomolar concentrations of ADIOL, was not modified by increasing concentrations of diethylstilboestrol up to 100 nM. This inhibition was counteracted by antiandrogens, which were unable to block the ADIOL stimulatory effect in steroid-free medium. On the other hand, in the presence of tamoxifen ADIOL showed an additive antiproliferative activity also in steroid-free medium, rather than the usual stimulatory effect. These results suggest that ADIOL stimulates breast cancer cell growth via oestrogen receptors, but inhibits oestrogen-stimulated growth via androgen receptors.
它们自身可刺激生长,但会抵消雌激素的生长刺激作用。针对其抑制作用,我们研究了5-烯-雄甾烯-3β,17β-二醇(ADIOL)在存在雌激素(雌二醇和己烯雌酚)、抗雌激素(他莫昔芬)和抗雄激素(羟基氟他胺)的情况下,对雌激素反应性MCF-7乳腺癌细胞生长的影响。用纳摩尔浓度的ADIOL实现的对雌激素刺激生长的抑制,在己烯雌酚浓度增加至100 nM时未发生改变。这种抑制作用可被抗雄激素抵消,而抗雄激素在无类固醇培养基中无法阻断ADIOL的刺激作用。另一方面,在存在他莫昔芬的情况下,ADIOL在无类固醇培养基中也表现出相加的抗增殖活性,而非通常的刺激作用。这些结果表明,ADIOL通过雌激素受体刺激乳腺癌细胞生长,但通过雄激素受体抑制雌激素刺激的生长。