Sánchez-Barceló Emilio J, Cos Samuel, Mediavilla Dolores, Martínez-Campa Carlos, González Alicia, Alonso-González Carolina
Department of Physiology and Pharmacology, School of Medicine, University of Cantabria, Santander, Spain.
J Pineal Res. 2005 May;38(4):217-22. doi: 10.1111/j.1600-079X.2004.00207.x.
In this article, we review the experimental data supporting an oncostatic role of melatonin on hormone-dependent mammary tumors. Beginning with the evidence on the role of estrogens in breast cancer etiology and mammary tumor growth, we summarize the actual therapeutic strategies with estrogens as a target. Additionally, we demonstrate that melatonin fulfills all the requirements to be considered as an antiestrogenic drug which shares properties with drugs of the two main pharmacological groups of substances which interact with the estrogen-signaling pathways such as: (i) drugs that act through the estrogen receptor interfering with the effects of endogenous estrogens; and (ii) drugs that interfere with the synthesis of estrogens by inhibiting the enzymes controlling the interconversion from their androgenic precursors. Furthermore, melatonin decreases circulating levels of estradiol. These three antiestrogenic mechanisms suggest that melatonin may have an important role in the prevention and treatment of hormone-dependent mammary cancer.
在本文中,我们回顾了支持褪黑素对激素依赖性乳腺肿瘤具有抑癌作用的实验数据。从雌激素在乳腺癌病因和乳腺肿瘤生长中的作用证据开始,我们总结了以雌激素为靶点的实际治疗策略。此外,我们证明褪黑素满足被视为抗雌激素药物的所有要求,它与与雌激素信号通路相互作用的两大类主要药理物质的药物具有共同特性,例如:(i)通过雌激素受体起作用、干扰内源性雌激素作用的药物;以及(ii)通过抑制控制雄激素前体相互转化的酶来干扰雌激素合成的药物。此外,褪黑素可降低雌二醇的循环水平。这三种抗雌激素机制表明褪黑素可能在激素依赖性乳腺癌的预防和治疗中发挥重要作用。