Department of Environmental Toxicology, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan.
Department of Clinical Research, National Hospital Organization Takasaki General Medical Center, 36 Takamatsu-cho, Takasaki, Gunma 370-0829, Japan.
Pharmacol Ther. 2023 Aug;248:108477. doi: 10.1016/j.pharmthera.2023.108477. Epub 2023 Jun 15.
Nuclear receptors (NR) collectively regulate several biological functions in various organs. While NRs can be characterized by activation of the transcription of their signature genes, they also have other diverse roles. Although most NRs are directly activated by ligand binding, which induces cascades of events leading to gene transcription, some NRs are also phosphorylated. Despite extensive investigations, primarily focusing on unique phosphorylation of amino acid residues in different NRs, the role of phosphorylation in the biological activity of NRs in vivo has not been firmly established. Recent studies on the phosphorylation of conserved phosphorylation motifs within the DNA- and ligand-binding domains confirmed has indicated the physiologically relevance of NR phosphorylation. This review focuses on estrogen and androgen receptors, and highlights the concept of phosphorylation as a drug target.
核受体 (NR) 共同调节各种器官的多种生物学功能。虽然 NR 可以通过其特征基因的转录激活来表征,但它们也具有其他不同的作用。虽然大多数 NR 可被配体结合直接激活,该激活诱导一系列导致基因转录的事件,但一些 NR 也可被磷酸化。尽管进行了广泛的研究,主要集中在不同 NR 中氨基酸残基的独特磷酸化上,但磷酸化在 NR 体内生物学活性中的作用尚未得到确定。最近关于 DNA 和配体结合域内保守磷酸化模体的磷酸化研究表明,NR 磷酸化具有生理相关性。这篇综述重点介绍了雌激素和雄激素受体,并强调了磷酸化作为药物靶点的概念。