首页> 外文期刊>Journal of pineal research >Melatonin modulates aromatase activity in MCF-7 human breast cancer cells.
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Melatonin modulates aromatase activity in MCF-7 human breast cancer cells.

机译:褪黑素调节MCF-7人乳腺癌细胞中的芳香化酶活性。

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Most of the current knowledge about the mechanisms by which melatonin inhibits the growth of breast cancer cells point to an interaction of melatonin with estrogen-responsive pathways, thus behaving as an antiestrogenic hormone. However, a possible effect of melatonin on the local synthesis of estrogens had not been examined. The objective of this work was to study whether melatonin may modify the aromatase activity in MCF-7 breast cancer cells thus modulating the local estrogen biosynthesis. In MCF-7 cells cultured with testosterone in estradiol-free media, melatonin (1 nM) counteracts the testosterone-induced cell proliferation dependent on the local biosynthesis of estrogens from testosterone by the aromatase activity of the cells. We found that melatonin reduces the aromatase activity (measured by the tritiated water release assay) of MCF-7 cells both at basal conditions and when aromatase activity was stimulated by cAMP or cortisol. The greatest inhibition of the aromatase activity was obtained with 1 nm melatonin, the same concentration that gives the highest antiproliferative and anti-invasive effects of MCF-7 cells. Finally, by RT-PCR, we found that melatonin downregulates aromatase expression at the transcriptional level in the MCF-7 cells. We conclude that melatonin, at physiological concentrations, decreases aromatase activity and expression in MCF-7 cells. This aromatase inhibitory effect of melatonin, together with its already known antiestrogenic properties interacting with the estrogen-receptor, makes this indoleamine an interesting tool to be considered in the prevention and treatment of hormone-dependent mammary neoplasias.
机译:当前关于褪黑素抑制乳腺癌细胞生长的机制的大多数知识都表明褪黑激素与雌激素反应性途径的相互作用,因此表现为一种抗雌激素激素。但是,尚未研究褪黑激素对雌激素局部合成的可能作用。这项工作的目的是研究褪黑激素是否可以改变MCF-7乳腺癌细胞中的芳香酶活性,从而调节局部雌激素的生物合成。在不含雌二醇的培养基中用睾丸激素培养的MCF-7细胞中,褪黑激素(1 nM)会通过细胞的芳香化酶活性来抵消睾丸激素诱导的细胞增殖,而后者依赖于睾丸激素从雌激素的局部生物合成。我们发现褪黑素在基础条件下以及cAMP或皮质醇刺激芳香酶活性时均会降低MCF-7细胞的芳香酶活性(通过by水释放测定法测量)。用1 nm褪黑激素可最大程度地抑制芳香化酶活性,该浓度与MCF-7细胞具有最高的抗增殖和抗侵袭作用的浓度相同。最后,通过RT-PCR,我们发现褪黑素在MCF-7细胞的转录水平上下调了芳香化酶的表达。我们得出的结论是,褪黑激素在生理浓度下会降低芳香化酶活性和MCF-7细胞中的表达。褪黑激素的这种芳香化酶抑制作用,以及与雌激素受体相互作用的已知抗雌激素特性,使得这种吲哚胺成为预防和治疗激素依赖性乳腺肿瘤的重要工具。

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