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糖皮质激素抵抗的分子机制。

Molecular mechanisms of glucocorticoid resistance.

机构信息

The Fourth Hospital of Hebei Medical University, Hebei Medical University, Shijiazhuang, China.

出版信息

Eur J Clin Invest. 2023 Feb;53(2):e13901. doi: 10.1111/eci.13901. Epub 2022 Nov 23.

Abstract

BACKGROUND

As a powerful anti-inflammatory, immunosuppressive, and antiproliferative drug, glucocorticoid (GC) plays an important role in the treatment of various diseases. However, some patients may experience glucocorticoid resistance (GCR) in clinical, and its molecular mechanism have not been determined.

METHODS

The authors performed a review of the literature on GCR focusing on mutations in the NR3C1 gene and impaired glucocorticoid receptor (GR) signalling, using METSTR (2000 through May 2022) to identify original articles and reviews on this topic. The search terms included 'glucocorticoid resistance/insensitive', 'steroid resistance/insensitive', 'NR3C1', and 'glucocorticoid receptor'.

RESULTS

Primary GCR is mainly caused by NR3C1 gene mutation, and 31 NR3C1 gene mutations have been reported so far. Secondary GCR is caused by impaired GC signalling pathways, including decreased expression of GR, impaired nuclear translocation of GR, and impaired binding of GR to GC and GR to target genes. However, the current research is more on the expression level of GR, and there are relatively few studies on other mechanisms. In addition, methods for improving GC sensitivity are rarely reported.

CONCLUSION

The molecular mechanisms of GCR are complex and may differ in different diseases or different patients. In future studies, when exploring the mechanism of GCR, methods to improve GC sensitivity should also be investigated.

摘要

背景

作为一种强大的抗炎、免疫抑制和抗增殖药物,糖皮质激素(GC)在治疗各种疾病中发挥着重要作用。然而,一些患者在临床中可能会出现糖皮质激素抵抗(GCR),其分子机制尚未确定。

方法

作者使用 METSTR(2000 年至 2022 年 5 月)对关于 NR3C1 基因突变和糖皮质激素受体(GR)信号转导受损导致 GCR 的文献进行了综述,以确定关于该主题的原始文章和综述。搜索词包括“糖皮质激素抵抗/不敏感”、“类固醇抵抗/不敏感”、“NR3C1”和“糖皮质激素受体”。

结果

原发性 GCR 主要由 NR3C1 基因突变引起,迄今为止已报道了 31 种 NR3C1 基因突变。继发性 GCR 是由 GC 信号通路受损引起的,包括 GR 表达减少、GR 核转位受损以及 GR 与 GC 和 GR 与靶基因的结合受损。然而,目前的研究更多地集中在 GR 的表达水平上,对其他机制的研究相对较少。此外,很少有报道改善 GC 敏感性的方法。

结论

GCR 的分子机制复杂,在不同疾病或不同患者中可能存在差异。在未来的研究中,当探索 GCR 的机制时,也应该研究提高 GC 敏感性的方法。

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