小干扰RNA技术在细胞色素P450基因调控中的应用。

IF 4.4 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Metabolism and Disposition Pub Date : 2025-03-01 Epub Date: 2025-01-21 DOI:10.1016/j.dmd.2025.100040
Wenzhao Jiang, Ruoyao Sang, Cai Zhang, Runting Yin, Zhen Ouyang, Yuan Wei
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引用次数: 0

摘要

细胞色素P450在内源性和外源性化学物质(包括药物和环境污染物)的生物转化中起着关键作用。p450的抑制和下调可以起到治疗作用,和/或调节药物代谢。p450在很大程度上被小分子抑制;然而,这种策略往往受到内在毒性和药物-药物相互作用的阻碍。此外,小分子要表现出高选择性和抑制效率是具有挑战性的。最近,小干扰RNA (siRNA)技术已经证明了P450调制的潜力。本文综述了sirna在P450基因调控中的最新应用实例。讨论了siRNA技术的必要性及其作为P450调节剂的优势,并对当前的障碍进行了回顾,并对未来的进展进行了展望。意义声明:本文综述了小干扰RNA技术在细胞色素P450基因调控中的应用研究。通过与小分子药物的比较,表明了siRNA方法的必要性及其作为P450调节剂的益处。此外,还审查了目前限制广泛实施本专题的挑战,并提出了对未来发展的展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of small interfering RNA technology in cytochrome P450 gene modulation.

Cytochrome P450 plays key roles in the biotransformation of endogenous and exogenous chemicals including drugs and environmental pollutants. The inhibition and downregulation of P450s can have therapeutic effects, and/or modulate drug metabolism. P450s are largely inhibited by small molecules; however, this strategy is often hampered by intrinsic toxicity and drug-drug interactions. Furthermore, it is challenging for small molecules to exhibit high selectivity and inhibitory efficiencies. Recently, small interfering RNA (siRNA) technology has demonstrated the potential for P450 modulation. Examples of recent applications of siRNAs in P450 gene modulation, in vitro and in vivo, are highlighted in this review. The necessity of siRNA techniques and their advantages as P450 modulators are discussed, along with a review of current obstacles and a perspective on future advancements. SIGNIFICANCE STATEMENT: This article reviews studies on the application of small interfering RNA technology to cytochrome P450 gene modulation. The necessity of siRNA methods and the benefits of their use as P450 modulators have been suggested by comparison with small-molecule drugs. Additionally, the challenges that presently limit the broader implementation of this topic are examined, and a perspective for future developments is proposed.

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来源期刊
CiteScore
6.50
自引率
12.80%
发文量
128
审稿时长
3 months
期刊介绍: An important reference for all pharmacology and toxicology departments, DMD is also a valuable resource for medicinal chemists involved in drug design and biochemists with an interest in drug metabolism, expression of drug metabolizing enzymes, and regulation of drug metabolizing enzyme gene expression. Articles provide experimental results from in vitro and in vivo systems that bring you significant and original information on metabolism and disposition of endogenous and exogenous compounds, including pharmacologic agents and environmental chemicals.
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