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In-Vitro Inhibition of Human Melanoma (BLM) Cell Growth by Progesterone Receptor Antagonist RU-486 (Mifepristone)

机译:孕激素受体拮抗剂RU-486(米非司酮)对人黑素瘤(BLM)细胞生长的体外抑制

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RU-486 is an abortifacient which is used to terminate early pregnancy. It acts by blocking progesterone receptor. In our earlier study with progesterone, RU-486 was used as a progesterone receptor antagonist to find out the mechanism of progesterone action on melanoma cells. Results indicated that the effect of progesterone was not mediated through progesterone receptor. In the course of experiments, it was observed that RU-486 by itself inhibited mouse melanoma cell growth. Further research work with RU-486 showed a dose dependent inhibition of human melanoma cell growth. The mechanism of inhibition of cell growth was due to apoptosis and this effect of RU-486 was neither mediated through progesterone receptor nor glucocorticoid receptor. This in-vitro study suggested that melanoma also could be a target for RU-486 action, apart from breast, ovary and prostate cancers.
机译:RU-486是一种堕胎药,用于终止早孕。它通过阻断孕激素受体起作用。在我们对孕激素的早期研究中,RU-486被用作孕激素受体拮抗剂,以了解孕激素作用于黑色素瘤细胞的机制。结果表明,孕激素的作用不是通过孕激素受体介导的。在实验过程中,观察到RU-486本身抑制小鼠黑素瘤细胞生长。 RU-486的进一步研究表明对人黑素瘤细胞的生长具有剂量依赖性抑制作用。抑制细胞生长的机制是由于细胞凋亡,RU-486的这种作用既不是通过孕激素受体也不是糖皮质激素受体介导的。这项体外研究表明,除乳腺癌,卵巢癌和前列腺癌外,黑色素瘤也可能是RU-486作用的靶标。

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