Langdon S P, Crew A J, Ritchie A A, Muir M, Wakeling A, Smyth J F, Miller W R
ICRF Medical Oncology Unit, Western General Hospital, Edinburgh, U.K.
Eur J Cancer. 1994;30A(5):682-6. doi: 10.1016/0959-8049(94)90545-2.
This paper presents results of the in vitro and in vivo effects of anti-oestrogens on the growth of human ovarian cancer cells. Tamoxifen and the "pure" anti-oestrogens, ICI 164,384 and ICI 182,780, inhibited the oestrogen-stimulated growth of the oestrogen receptor (ER)-positive PE04 and PE01 cell lines grown in culture, the latter two compounds being more potent than tamoxifen. In the absence of 17 beta-oestradiol (E2), tamoxifen, but not the pure anti-oestrogens, produced a small degree of growth stimulation in the PE01 and PE04 lines at concentrations between 10((7) and 10(-9) M. In contrast, growth of the ER-negative PE014 line was unaffected by E2 and all three anti-oestrogens. The effects of tamoxifen and ICI 182,780 on PE04 cells grown as xenografts in nude mice were also studied. Both anti-oestrogens produce significant growth inhibitory effects. These results indicate that ovarian carcinoma cells may be sensitive to anti-oestrogens in vitro and in vivo, and support the view that anti-oestrogens merit further clinical studies in patients with ER-positive tumours.
本文介绍了抗雌激素对人卵巢癌细胞生长的体外和体内作用结果。他莫昔芬以及“纯”抗雌激素ICI 164,384和ICI 182,780抑制了培养中生长的雌激素受体(ER)阳性PE04和PE01细胞系的雌激素刺激生长,后两种化合物比他莫昔芬更有效。在不存在17β-雌二醇(E2)的情况下,他莫昔芬而非纯抗雌激素在10^(-7)至10^(-9) M的浓度下对PE01和PE04细胞系产生了一定程度的生长刺激。相比之下,ER阴性的PE014细胞系的生长不受E2和所有三种抗雌激素的影响。还研究了他莫昔芬和ICI 182,780对裸鼠体内作为异种移植物生长的PE04细胞的影响。两种抗雌激素均产生显著的生长抑制作用。这些结果表明,卵巢癌细胞在体外和体内可能对抗雌激素敏感,并支持抗雌激素值得对ER阳性肿瘤患者进行进一步临床研究的观点。