糖皮质激素受体作为经典和新型抗炎治疗的靶点。

Andrew C B Cato, Heike Schäcke, Wolfram Sterry, Khusru Asadullah
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引用次数: 18

摘要

糖皮质激素以其有效的抗炎和免疫抑制作用而闻名。由于严重的副作用,它们的临床用途仍然有限,因此需要寻找提高其收益风险比的方法。从机制上讲,糖皮质激素通过与细胞内受体(糖皮质激素受体)相互作用发挥作用,糖皮质激素受体是一种配体调节的转录因子,可以积极或消极地改变特定基因的表达。虽然人们普遍认为,这种受体的独特负调节作用形成了糖皮质激素预期的抗炎作用的基础,但对这种受体的功能导致其副作用知之甚少。许多细胞代谢控制基因受到糖皮质激素的正调控,这一事实使得基因表达的正调控成为抑制不良反应的一种有吸引力的作用方式。然而,糖皮质激素对基因表达的正向调节是通过不同的机制和细胞类型特异性的方式发生的,因此很难在一个单一的分析过程中预测其可能的生物学效应。在受体分子作用方面的最新进展逐渐揭示了不同的测定方法和重要特征,这些特征可以放在一起确定糖皮质激素受体不同转激活功能的生理后果。这些将为寻找具有有效抗炎但副作用较小的糖皮质激素受体激动剂提供宝贵的信息来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The glucocorticoid receptor as target for classic and novel anti-inflammatory therapy.
Glucocorticoids are well known for their potent anti-inflammatory and immune-suppressive actions. Their clinical usefulness remains limited due to serious side effects that have necessitated a search for ways of improving their benefit-risk ratios. Mechanistically, glucocorticoids function by interacting with an intracellular receptor, the glucocorticoid receptor, a ligand-regulated transcription factor that positively or negatively alters the expression of specific genes. While it is well accepted that distinct negative regulatory action of this receptor forms the basis of the desired anti-inflammatory effects of glucocorticoids, not much is known about the function of the receptor that contributes to its side effects. The fact that a number of cellular metabolic control genes are positively regulated by glucocorticoids makes positive regulation of gene expression an attractive mode of action for the adverse effects. Positive regulation of gene expression by glucocorticoids, however, occurs through different mechanisms and in cell-type specific manner making it difficult to predict its possible biological effects in one single assay procedure. Recent advances in the molecular action of the receptor are gradually revealing different assays and important characteristics that can be put together in determining the physiological consequences of the different transactivation functions of the glucocorticoid receptor. These will provide invaluable source of information for the search of glucocorticoid receptor agonists with potent anti-inflammatory but reduced side effects.
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