Navigating a plethora of progesterone receptors: Comments on the safety/risk of progesterone supplementation in women with a history of breast cancer or at high-risk for developing breast cancer

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Caroline H. Diep , Laura J. Mauro , Carol A. Lange
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引用次数: 0

Abstract

Progesterone and progestin agonists are potent steroid hormones. There are at least three major types of progesterone receptor (PR) families that interact with and respond to progesterone or progestin ligands. These receptors include ligand-activated transcription factor isoforms (PR-A and PR-B) encoded by the PGR gene, often termed classical or nuclear progesterone receptor (nPR), membrane-spanning progesterone receptor membrane component proteins known as PGRMC1/2, and a large family of progestin/adipoQ receptors or PAQRs (also called membrane PRs or mPRs). Cross-talk between mPRs and nPRs has also been reported. The complexity of progesterone actions via a plethora of diverse receptors warrants careful consideration of the clinical applications of progesterone, which primarily include birth control formulations in young women and hormone replacement therapy following menopause. Herein, we focus on the benefits and risk of progesterone/progestin supplementation. We conclude that progesterone-only supplementation is considered safe for most reproductive-age women. However, women who currently have ER + breast cancer or have had such cancer in the past should not take sex hormones, including progesterone. Women at high-risk for developing breast or ovarian cancer, either due to their family history or known genetic factors (such as BRCA1/2 mutation) or hormonal conditions, should avoid exogenous sex hormones and proceed with caution when considering using natural hormones to mitigate menopausal symptoms and/or improve quality of life after menopause. These individuals are urged to consult with a qualified OB-GYN physician to thoroughly assess the risks and benefits of sex hormone supplementation. As new insights into the homeostatic roles and specificity of highly integrated rapid signaling and nPR actions are revealed, we are hopeful that the benefits of using progesterone use may be fully realized without an increased risk of women’s cancer.

驾驭过多的黄体酮受体:对有乳腺癌症病史或患癌症高危女性补充黄体酮的安全性/风险的评论。
孕激素和孕激素激动剂是强效类固醇激素。至少有三种主要类型的黄体酮受体家族与黄体酮或孕激素配体相互作用并对其作出反应。这些受体包括由PGR基因编码的配体激活的转录因子亚型(PR-A和PR-B),通常称为经典或核孕激素受体(nPR),称为PGRMC1/2的跨膜孕激素受体膜组分蛋白,以及一大家族的孕激素/脂肪Q受体或PAQRs(也称为膜PRs或mPRs)。还报道了mPR和nPR之间的串扰。黄体酮通过大量不同受体发挥作用的复杂性,需要仔细考虑黄体酮的临床应用,其中主要包括年轻女性的节育配方和更年期后的激素替代疗法。在此,我们关注补充黄体酮/孕激素的益处和风险。我们得出的结论是,仅补充黄体酮被认为对大多数育龄妇女是安全的。然而,目前患有ER的女性 + 癌症或曾患过此类癌症者,不应服用性激素,包括孕酮。由于家族史或已知遗传因素(如BRCA1/2突变)或激素状况,患有乳腺癌或卵巢癌癌症的高危女性应避免使用外源性激素,并在考虑使用天然激素缓解更年期症状和/或改善更年期后的生活质量时谨慎行事。敦促这些人咨询合格的OB-GYN医生,以彻底评估补充性激素的风险和益处。随着对高度整合的快速信号传导和nPR作用的稳态作用和特异性的新见解的揭示,我们希望使用孕酮的好处可以完全实现,而不会增加女性癌症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Steroids
Steroids 医学-内分泌学与代谢
CiteScore
5.10
自引率
3.70%
发文量
120
审稿时长
73 days
期刊介绍: STEROIDS is an international research journal devoted to studies on all chemical and biological aspects of steroidal moieties. The journal focuses on both experimental and theoretical studies on the biology, chemistry, biosynthesis, metabolism, molecular biology, physiology and pharmacology of steroids and other molecules that target or regulate steroid receptors. Manuscripts presenting clinical research related to steroids, steroid drug development, comparative endocrinology of steroid hormones, investigations on the mechanism of steroid action and steroid chemistry are all appropriate for submission for peer review. STEROIDS publishes both original research and timely reviews. For details concerning the preparation of manuscripts see Instructions to Authors, which is published in each issue of the journal.
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