Drug regulation of microRNA

A. Abaturov, V. Babуch
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Abstract

The scientific review provides the mechanisms of drug regulation of microRNA in the human body. To write the article, information was searched using Scopus, Web of Science, MEDLINE, PubMed, Google Scholar, Embase, Global Health, The Cochrane Library databases. To restore the reduced functional activity of microRNAs, replacement therapy is used, with modified synthetic analogs of endogenous microRNAs, and drugs that enhance the production of the body’s own microRNAs. The authors state that numerous studies have confirmed the effectiveness of miRNA replacement therapy. It is known that there are several groups of drugs among miRNA inhibitors: anti-miRNA oligonucleotides, miRNA traps, miRNA mimics that prevent miRNA binding; peptide nucleic acids, small-molecule inhibitors. The authors suggest that the expression of drug-metabolizing enzymes is controlled by nuclear receptors and transcription factors, epigenetic regulation such as DNA methylation and histone acetylation, and post-translational modification. It is emphasized that ursodeoxycholic acid modulates the expression of some miRNAs. It is known that probiotic bacteria can modulate the expression level of miRNA genes. The use of probiotics is accompanied by a change in the expression of nume­rous genes of the body involved in the regulation of the inflammatory response, allergic reactions, metabolism and other biological processes. Thus, modern science is intensively studying the potential of using drugs that restore miRNA content or inhibit miRNA acti­vity for the therapy of miRNA-dependent conditions. The results of scientific research confirmed the therapeutic effect of ursodeoxycholic acid and probiotic preparations due to the effect on the acti­vity of miRNA generation in hepatobiliary diseases. Therefore, the introduction into clinical practice of drugs than can modulate the content and expression of specific miRNAs will certainly open new perspectives in the treatment of patients with hepatobiliary diseases.
药物对 microRNA 的调控
这篇科学综述介绍了人体内 microRNA 的药物调控机制。撰写本文时,使用了 Scopus、Web of Science、MEDLINE、PubMed、Google Scholar、Embase、Global Health、The Cochrane Library 等数据库进行信息检索。为了恢复功能减弱的 microRNAs 活性,人们使用了替代疗法,包括内源性 microRNAs 的改良合成类似物,以及提高人体自身 microRNAs 产量的药物。作者指出,许多研究已经证实了 miRNA 替代疗法的有效性。众所周知,miRNA 抑制剂中有几类药物:抗 miRNA 寡核苷酸、miRNA 陷阱、阻止 miRNA 结合的 miRNA 模拟物;肽核酸、小分子抑制剂。作者认为,药物代谢酶的表达受核受体和转录因子、DNA 甲基化和组蛋白乙酰化等表观遗传调控以及翻译后修饰的控制。有研究强调,熊去氧胆酸可调节某些 miRNA 的表达。众所周知,益生菌可以调节 miRNA 基因的表达水平。在使用益生菌的同时,体内许多参与调节炎症反应、过敏反应、新陈代谢和其他生物过程的基因的表达也会发生变化。因此,现代科学正在深入研究使用恢复 miRNA 含量或抑制 miRNA 活性的药物治疗 miRNA 依赖性疾病的潜力。科学研究结果证实,熊去氧胆酸和益生菌制剂对肝胆疾病中 miRNA 生成活性的影响具有治疗效果。因此,将能够调节特定 miRNA 含量和表达的药物引入临床实践,必将为肝胆疾病患者的治疗开辟新的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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