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2-甲氧基雌二醇与女性生殖组织疾病

2-methoxyestradiol and disorders of female reproductive tissues.

作者信息

Pinto Mauricio P, Medina Rodolfo A, Owen Gareth I

机构信息

Departamento de Fisiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

Horm Cancer. 2014 Oct;5(5):274-83. doi: 10.1007/s12672-014-0181-2. Epub 2014 Apr 25.

Abstract

2-Methoxyestradiol (2ME) is an endogenous metabolite of 17β-estradiol. Once thought of as a mere degradation product, 2ME has gained attention as an important component of reproductive physiology and as a therapeutic agent in reproductive pathologies such as preeclampsia, endometriosis, infertility, and cancer. In this review, we discuss the involvement of 2ME in reproductive pathophysiology and summarize its known mechanisms of action: microtubule disruption, inhibition of angiogenesis and stimulation of apoptosis. Currently, the clinical uses of 2ME as a single agent are limited due to its poor water solubility and thus low bioavailability; however, 2ME analogs and derivatives have been recently developed and tested as cancer treatments. Despite some isolated success stories and ongoing research, 2ME derivatives have not yet provided the expected results. The adjuvant use of 2ME derivatives with chemotherapeutic agents is hindered by their intrinsic toxicity confounding the unwanted secondary effects of chemotherapy. However, due to the well-tested tolerance of the body to high doses of native 2ME, it may the combination of native 2ME with conventional treatments that will offer novel clinically relevant regimens for cancer and other reproductive disorders.

摘要

2-甲氧基雌二醇(2ME)是17β-雌二醇的内源性代谢产物。2ME曾一度被认为仅仅是一种降解产物,如今却作为生殖生理学的重要组成部分以及子痫前期、子宫内膜异位症、不孕症和癌症等生殖系统疾病的治疗药物而受到关注。在本综述中,我们讨论了2ME在生殖病理生理学中的作用,并总结了其已知的作用机制:微管破坏、血管生成抑制和细胞凋亡刺激。目前,2ME作为单一药物的临床应用受到其水溶性差因而生物利用度低的限制;然而,2ME类似物和衍生物最近已被开发并作为癌症治疗药物进行测试。尽管有一些个别成功案例且研究仍在进行,但2ME衍生物尚未取得预期效果。2ME衍生物与化疗药物的联合使用受到其内在毒性的阻碍,这种毒性会混淆化疗的不良副作用。然而,由于人体对高剂量天然2ME具有经过充分测试的耐受性,可能是天然2ME与传统治疗方法的联合使用将为癌症和其他生殖系统疾病提供新的具有临床相关性的治疗方案。

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