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类固醇在正常细胞和恶性细胞中缺乏选择性杀伤作用。

Lack of selective killing by steroids in normal and malignant cells.

作者信息

Weichselbaum R R, Little J B, Nove J, Hellman S, Piro A J

出版信息

J Cell Physiol. 1980 Jun;103(3):429-33. doi: 10.1002/jcp.1041030308.

Abstract

Using a colony formation assay, the cytotoxic effects of steroids and an anti-steroid on an established human breast tumor line and two human diploid fibroblast strains were studied. Experiments involving 17 a-estradiol, 17 beta-estradiol, dexamethasone, cortisone, dihydrotestosterone, and the anti-estrogen Tamoxifen showed no killing at concentrations below 10(-7)M following a 24-hour exposure to these agents. A maximum of 80% killing was observed at 10(-5)M with dexamethasone in one fibroblast strain and at the same dose of 17 beta-estradiol in the breast tumor line. The extent of killing observed is insufficient to account for many of the clinical remissions observed with steroid therapy. The data also suggest that at therapeutic doses, there is no selective killing of malignant cells by these agents.

摘要

采用集落形成试验,研究了类固醇和一种抗类固醇对一种已建立的人乳腺肿瘤细胞系和两种人二倍体成纤维细胞系的细胞毒性作用。涉及17α-雌二醇、17β-雌二醇、地塞米松、可的松、二氢睾酮和抗雌激素他莫昔芬的实验表明,在这些药物暴露24小时后,浓度低于10^(-7)M时没有杀伤作用。在一种成纤维细胞系中,地塞米松浓度为10^(-5)M时观察到最大80%的杀伤率,在乳腺肿瘤细胞系中,17β-雌二醇相同剂量时也观察到最大80%的杀伤率。观察到的杀伤程度不足以解释类固醇治疗中观察到的许多临床缓解情况。数据还表明,在治疗剂量下,这些药物不会选择性杀伤恶性细胞。

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