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芳香化酶抑制剂:乳腺癌治疗的过去、现在与未来

Aromatase inhibitors: past, present and future in breast cancer therapy.

作者信息

Dutta Udayan, Pant Kartikeya

机构信息

Department of Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Med Oncol. 2008;25(2):113-24. doi: 10.1007/s12032-007-9019-x. Epub 2007 Nov 1.

Abstract

Estrogen has been implicated in promoting breast cancer in a majority of women. Endocrine therapy controlling estrogen production has been the guiding principle in treating breast cancer for more than a century. A greater understanding of this disease at a molecular level has led to the development of molecules that inhibit estrogen production by inhibiting the aromatase enzyme, that is the primary source of estrogen in postmenopausal women. This review examines the evolution of aromatase inhibitor (AI) based therapies over the past three decades. The third generation aromatase inhibitors (anastrozole, letrozole and exemestane), which have been found to be extremely specific and effective in an adjuvant/neoadjuvant/extended adjuvant setting are discussed from a biochemical and clinical perspective. A comprehensive discussion of the past, present, and future of aromatase inhibitors is conducted in this review.

摘要

雌激素被认为在大多数女性乳腺癌的发生发展中起作用。控制雌激素产生的内分泌治疗在乳腺癌治疗中作为指导原则已逾一个多世纪。对这种疾病在分子水平上的更深入了解促使了一些分子的研发,这些分子通过抑制芳香化酶来抑制雌激素的产生,芳香化酶是绝经后女性雌激素的主要来源。本综述探讨了过去三十年中基于芳香化酶抑制剂(AI)的治疗方法的演变。从生化和临床角度讨论了第三代芳香化酶抑制剂(阿那曲唑、来曲唑和依西美坦),它们在辅助/新辅助/延长辅助治疗环境中已被发现具有极高的特异性和有效性。本综述对芳香化酶抑制剂的过去、现在和未来进行了全面讨论。

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