Department of Pharmacodynamics and Biopharmacy, Faculty of Pharmacy, University of Szeged, P.O. Box: 0000-000, Szeged, Hungary.
Anticancer Agents Med Chem. 2018;18(5):652-666. doi: 10.2174/1871520617666171114111721.
Research of steroidal compounds as anticancer agents started almost 50 years ago. During the past decades, several innovative new steroids, like cyproterone, finasteride, estramustin, exemestane and fulvestrant have successfully become a part of routine clinical practice. Meanwhile, a vast amount of new information have accumulated about the functions of the endogenous steroid system (including the characterization of enzymes, receptors, transcription pathways, etc.) and about the role of steroids in carcinogenesis. Therefore, it is regularly required to review the latest published results, focusing on a well-defined part within this research field that has definitely developed into a highly diversified speciality by now. Herein, we make an attempt to summarize the most recent results reported about anticancer agents of estrane backbone, focusing on their mechanisms of action and their structure-activity relationships. Due to the vast number and various accessibilities of scientific publications, neither other reviews nor this one can be considered as absolutely exhaustive. In spite of these restrictive factors, the current review makes a good opportunity to define the recent scientific trends in the field of estradiol-related anticancer agents.
甾体化合物作为抗癌药物的研究始于近 50 年前。在过去的几十年中,几种创新的新型甾体药物,如环丙孕酮、非那雄胺、雌莫司汀、依西美坦和氟维司群,已成功成为常规临床实践的一部分。同时,关于内源性甾体系统的功能(包括酶、受体、转录途径等的特征)以及甾体在致癌作用中的作用,积累了大量新信息。因此,需要定期审查最新发表的结果,重点关注该研究领域内一个已经发展成为高度多样化专业领域的明确部分。在这里,我们尝试总结最近报道的甾体骨架抗癌药物的最新结果,重点关注它们的作用机制和结构-活性关系。由于科学出版物的数量众多且种类繁多,因此其他评论和本文都不能被认为是绝对详尽的。尽管存在这些限制因素,但本次综述为确定与雌二醇相关的抗癌药物领域的最新科学趋势提供了一个很好的机会。