Competitive and compensatory effects of androgen signaling and glucocorticoid signaling

Naoki Harada, H. Inui, R. Yamaji
{"title":"Competitive and compensatory effects of androgen signaling and glucocorticoid signaling","authors":"Naoki Harada, H. Inui, R. Yamaji","doi":"10.14800/RCI.785","DOIUrl":null,"url":null,"abstract":"Androgens and glucocorticoids have competitive and compensatory effects in several physiological and pathophysiological processes.  Although blood androgen levels affect blood glucocorticoid levels and vice versa, it does not fully explain the relationship between the effects of androgens and glucocorticoids.  Androgens and glucocorticoids exert their functions through binding to androgen receptor (AR) and glucocorticoid receptor (GR), respectively.  AR homodimer and GR homodimer bind to the androgen response element (ARE) and glucocorticoid response element (GRE), respectively, where they positively or negatively regulate transcription.  AR/GR heterodimer can also form but whether it has a physiological role is unclear.  Notably, some ARE/GRE sites are recognized by both AR and GR.  This review focuses on the functional interventions between androgen signaling and glucocorticoid signaling in target cells that are involved in muscle atrophy, lipid metabolism in adipocytes and hepatocytes, and pancreatic β-cell death.  Androgens and glucocorticoids exert opposite effects by differentially regulating key genes ( e.g. , insulin-like growth factor-1, atrogin-1, and thioredoxin-interacting protein) involved in these physiological processes.  We also review functional compensation between these steroids in the development of castration-resistant prostate cancer in which glucocorticoids compensate for the castration-induced loss of AR function by activating key genes ( e.g. , serum/glucocorticoid-regulated kinase 1).  The gene expressions regulated by androgens and glucocorticoids are regulated through at least three different mechanisms in target cells: (i) regulation of applicable ligand levels by modulation of steroid metabolite enzyme levels, (ii) regulation of each other's receptor levels, and (iii) competitive binding between AR and GR on ARE/GRE sites.  Recent findings shed light on the complicated relationship between androgen signaling and glucocorticoid signaling in various cellular processes.","PeriodicalId":20980,"journal":{"name":"Receptors and clinical investigation","volume":"60 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Receptors and clinical investigation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14800/RCI.785","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Androgens and glucocorticoids have competitive and compensatory effects in several physiological and pathophysiological processes.  Although blood androgen levels affect blood glucocorticoid levels and vice versa, it does not fully explain the relationship between the effects of androgens and glucocorticoids.  Androgens and glucocorticoids exert their functions through binding to androgen receptor (AR) and glucocorticoid receptor (GR), respectively.  AR homodimer and GR homodimer bind to the androgen response element (ARE) and glucocorticoid response element (GRE), respectively, where they positively or negatively regulate transcription.  AR/GR heterodimer can also form but whether it has a physiological role is unclear.  Notably, some ARE/GRE sites are recognized by both AR and GR.  This review focuses on the functional interventions between androgen signaling and glucocorticoid signaling in target cells that are involved in muscle atrophy, lipid metabolism in adipocytes and hepatocytes, and pancreatic β-cell death.  Androgens and glucocorticoids exert opposite effects by differentially regulating key genes ( e.g. , insulin-like growth factor-1, atrogin-1, and thioredoxin-interacting protein) involved in these physiological processes.  We also review functional compensation between these steroids in the development of castration-resistant prostate cancer in which glucocorticoids compensate for the castration-induced loss of AR function by activating key genes ( e.g. , serum/glucocorticoid-regulated kinase 1).  The gene expressions regulated by androgens and glucocorticoids are regulated through at least three different mechanisms in target cells: (i) regulation of applicable ligand levels by modulation of steroid metabolite enzyme levels, (ii) regulation of each other's receptor levels, and (iii) competitive binding between AR and GR on ARE/GRE sites.  Recent findings shed light on the complicated relationship between androgen signaling and glucocorticoid signaling in various cellular processes.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
雄激素信号和糖皮质激素信号的竞争和补偿作用
雄激素和糖皮质激素在一些生理和病理生理过程中具有竞争性和代偿性作用。虽然血液中的雄激素水平会影响血液中的糖皮质激素水平,反之亦然,但这并不能完全解释雄激素和糖皮质激素的作用之间的关系。雄激素和糖皮质激素分别通过与雄激素受体(AR)和糖皮质激素受体(GR)结合发挥作用。AR同型二聚体和GR同型二聚体分别与雄激素反应元件(ARE)和糖皮质激素反应元件(GRE)结合,在那里它们正向或负向调节转录。AR/GR异源二聚体也可形成,但其是否具有生理作用尚不清楚。值得注意的是,一些ARE/GRE位点同时被AR和GR识别。本文将重点讨论雄激素信号和糖皮质激素信号在参与肌肉萎缩、脂肪细胞和肝细胞脂质代谢以及胰腺β细胞死亡的靶细胞中的功能干预。雄激素和糖皮质激素通过不同地调节参与这些生理过程的关键基因(如胰岛素样生长因子-1、抗血小板激素-1和硫氧还蛋白相互作用蛋白)来发挥相反的作用。我们还回顾了这些类固醇在去势抵抗性前列腺癌发展过程中的功能补偿,其中糖皮质激素通过激活关键基因(例如血清/糖皮质激素调节的激酶1)来补偿去势诱导的AR功能丧失。雄激素和糖皮质激素调节的基因表达在靶细胞中至少通过三种不同的机制进行调节:(i)通过调节类固醇代谢物酶水平来调节适用的配体水平,(ii)相互调节受体水平,以及(iii) AR和GR在ARE/GRE位点上的竞争性结合。最近的研究结果揭示了雄激素信号和糖皮质激素信号在各种细胞过程中的复杂关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The role of leptin in the central nervous system remyelination 20 Years Anniversary for SORLA/SORL1 (1996-2016) Targeting sympathetic glia for treating cardiovascular diseases Computational analysis in Influenza virus HIF-1α promotes NSCs migration by modulating Slit2-Robo1 signaling after cerebral ischemia
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1