天然产物在慢性疾病治疗中的作用:调控KEAP1-NRF2通路的作用

IF 5.5
The American journal of Chinese medicine Pub Date : 2025-01-01 Epub Date: 2025-01-29 DOI:10.1142/S0192415X25500041
Yaling Li, Xijia Wang, Shuyue Li, Lei Wang, Ningning Ding, Yali She, Changtian Li
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引用次数: 0

摘要

氧化应激在许多慢性疾病的发病机制中起着关键作用。kelch样ech相关蛋白1-转录因子NF-E2 p45-相关因子2 (KEAP1-NRF2)通路在维持氧化还原稳态和调节多种生物过程如炎症、蛋白稳态和代谢稳态中起着至关重要的作用。在本文中,我们介绍了最近关于KEAP1-NRF2通路的研究发现,该通路在神经退行性疾病、心血管疾病、代谢性疾病、呼吸系统疾病、消化系统疾病和癌症等多种疾病中被异常调控并诱导氧化应激损伤。鉴于这些证据,靶向KEAP1-NRF2代表了开发慢性疾病治疗策略的一个非常有前途的途径,因此基于靶向NRF2途径开发适当的治疗策略已经成为一个重要的研究兴趣领域。本文综述了目前KEAP1-NRF2的调控策略,以及天然化合物和中药的最新研究进展,以期为靶向KEAP1-NRF2的药物发现和开发提供有意义的指导。此外,本文还讨论了利用NRF2作为治疗靶点所面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Effects of Natural Products in the Treatment of Chronic Diseases: The Role in Regulating KEAP1-NRF2 Pathway.

Oxidative stress represents a pivotal mechanism in the pathogenesis of numerous chronic diseases. The Kelch-like ECH-associated protein 1-transcription factor NF-E2 p45-related factor 2 (KEAP1-NRF2) pathway plays a crucial role in maintaining redox homeostasis and regulating a multitude of biological processes such as inflammation, protein homeostasis, and metabolic homeostasis. In this paper, we present the findings of recent studies on the KEAP1-NRF2 pathway, which have revealed that it is aberrantly regulated and induces oxidative stress injury in a variety of diseases such as neurodegenerative diseases, cardiovascular diseases, metabolic diseases, respiratory diseases, digestive diseases, and cancer. Given this evidence, targeting KEAP1-NRF2 represents a highly promising avenue for developing therapeutic strategies for chronic diseases, and thus the development of appropriate therapeutic strategies based on the targeting of the NRF2 pathway has emerged as a significant area of research interest. This paper highlights an overview of current strategies to modulate KEAP1-NRF2, as well as recent advances in the use of natural compounds and traditional Chinese medicine, with a view to providing meaningful guidelines for drug discovery and development targeting KEAP1-NRF2. Additionally, it discusses the challenges associated with harnessing NRF2 as a therapeutic target.

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