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一种新型抗雌激素(类似物II)对人乳腺癌细胞的抗肿瘤活性。

Antitumor activity of a novel antiestrogen (Analog II) on human breast cancer cells.

作者信息

Jain P T, Rajah T T, Pento J T

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, University of Oklahoma, Oklahoma City 73190, USA.

出版信息

Anticancer Drugs. 1997 Nov;8(10):964-73. doi: 10.1097/00001813-199711000-00008.

Abstract

Analog II (1,1-dichloro-cis-2,3-diarylcyclopropane), previously shown to be a pure antiestrogen in mice, was examined for potential antitumor activity on human breast cancer cells in culture. In this study, Analog II produced a dose-related antiproliferative effect on the growth of estrogen receptor (ER)-positive MCF-7 human breast cancer cells over a concentration range of 10(-11) to 10(-5) M. Analog II increased the fraction of MCF-7 cells in the G2/M phase of the cell cycle. Further, this compound inhibited the growth of ER-negative MDA-MB-231 human breast cancer cells over a concentration range of 10(-9) to 10(-6) M. Using scanning electron microscopy to evaluate drug-induced changes in cellular morphology, it was observed that Analog II decreased the length and density of microvilli on both MCF-7 and MDA-MB-231 cells. The effects of Analog II on MCF-7 and MDA-MB-231 cell proliferation and morphology were not reversed in the presence of estradiol. In addition, the induction of estrogen-dependent genes in MCF-7 cells was not reversed by Analog II. It was observed that non-specific cytotoxicity may be responsible for part of the Analog II-induced inhibition on MCF-7 and MDA-MB-231 cell proliferation. However, the antitumor activity of this compound was found to be specific to human breast cancer cells since it did not alter the proliferation or viability of non-breast A-549 human lung cancer cells. In conclusion, these results indicate that Analog II is a potent antitumor agent, has a unique antitumor mechanism in breast cancer cells and may be effective in the treatment of breast cancer.

摘要

类似物II(1,1 - 二氯 - 顺式 - 2,3 - 二芳基环丙烷),先前已证明在小鼠中是一种纯抗雌激素药物,现对其在培养的人乳腺癌细胞上的潜在抗肿瘤活性进行研究。在本研究中,类似物II在10^(-11)至10^(-5) M的浓度范围内,对雌激素受体(ER)阳性的MCF - 7人乳腺癌细胞的生长产生了剂量相关的抗增殖作用。类似物II增加了处于细胞周期G2/M期的MCF - 7细胞比例。此外,该化合物在10^(-9)至10^(-6) M的浓度范围内抑制了ER阴性的MDA - MB - 231人乳腺癌细胞的生长。使用扫描电子显微镜评估药物诱导的细胞形态变化,观察到类似物II降低了MCF - 7和MDA - MB - 231细胞上微绒毛的长度和密度。在存在雌二醇的情况下,类似物II对MCF - 7和MDA - MB - 231细胞增殖及形态的影响并未逆转。此外,类似物II也未逆转MCF - 7细胞中雌激素依赖性基因的诱导。观察到非特异性细胞毒性可能是类似物II诱导的对MCF - 7和MDA - MB - 231细胞增殖抑制的部分原因。然而,发现该化合物的抗肿瘤活性对人乳腺癌细胞具有特异性,因为它不会改变非乳腺的A - 549人肺癌细胞的增殖或活力。总之,这些结果表明类似物II是一种有效的抗肿瘤药物,在乳腺癌细胞中具有独特的抗肿瘤机制,可能对乳腺癌治疗有效。

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