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抗雌激素在体外及异种移植模型中对雌激素受体阳性人卵巢癌的生长抑制作用

Growth inhibition of oestrogen receptor-positive human ovarian carcinoma by anti-oestrogens in vitro and in a xenograft model.

作者信息

Langdon S P, Crew A J, Ritchie A A, Muir M, Wakeling A, Smyth J F, Miller W R

机构信息

ICRF Medical Oncology Unit, Western General Hospital, Edinburgh, U.K.

出版信息

Eur J Cancer. 1994;30A(5):682-6. doi: 10.1016/0959-8049(94)90545-2.

Abstract

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.

摘要

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。

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