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比较雄激素受体和糖皮质激素受体的作用机制。

Comparing the rules of engagement of androgen and glucocorticoid receptors.

作者信息

Claessens Frank, Joniau Steven, Helsen Christine

机构信息

Molecular Endocrinology Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Campus GHB ON1, Herestraat 49, PO Box 901, 3000, Leuven, Belgium.

Department of Urology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.

出版信息

Cell Mol Life Sci. 2017 Jun;74(12):2217-2228. doi: 10.1007/s00018-017-2467-3. Epub 2017 Feb 6.

Abstract

Despite the diverse physiological activities of androgens and glucocorticoids, the corresponding receptors are very close members of the nuclear-receptor super family. Their action mechanisms show striking similarities, since both receptors recognize very similar DNA-response elements and recruit the same coactivators to their target genes. The specificity of the responses lies mainly in the tissue-specific expression of the receptors and in their ligand specificity. In cells, where both receptors are expressed, the mechanisms leading to the difference in target genes are less obvious. They lie in part in subtle variations of the DNA-binding sites, in cooperativity with other transcription factors and in differential allosteric signals from the DNA and ligand to other receptor domains. We will highlight the different suggestions that might explain the DNA sequence selectivity and will compare the possible allosteric routes between the response elements and the different functions in the transactivation process. The interplay of androgen and glucocorticoid receptors is also highly relevant in clinical settings, where both receptors are therapeutically targeted. We will discuss the possibility that the glucocorticoid and androgen receptors can play partially redundant roles in castration-resistant prostate cancer.

摘要

尽管雄激素和糖皮质激素具有多种生理活性,但相应的受体却是核受体超家族中关系非常密切的成员。它们的作用机制表现出惊人的相似性,因为这两种受体都识别非常相似的DNA反应元件,并将相同的共激活因子募集到其靶基因上。反应的特异性主要在于受体的组织特异性表达及其配体特异性。在同时表达这两种受体的细胞中,导致靶基因差异的机制不太明显。部分原因在于DNA结合位点的细微变化、与其他转录因子的协同作用以及来自DNA和配体到其他受体结构域的不同变构信号。我们将强调可能解释DNA序列选择性的不同观点,并比较反应元件与反式激活过程中不同功能之间可能的变构途径。雄激素和糖皮质激素受体的相互作用在临床环境中也高度相关,在临床中这两种受体都是治疗靶点。我们将讨论糖皮质激素受体和雄激素受体在去势抵抗性前列腺癌中可能发挥部分冗余作用的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9dd/11107546/82c529033a47/18_2017_2467_Fig1_HTML.jpg

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