靶向Keap1/Nrf2轴在癌症中的作用:分子机制和药理干预。

IF 2.7 3区 医学 Q2 ONCOLOGY
Yangchen Xia, Ziyang Xu, Xun Yuan, Qian Chu
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引用次数: 0

摘要

转录因子核因子-红细胞2相关因子2 (Nrf2)是多种细胞保护途径的一线调节因子,如炎症、氧化还原代谢和蛋白质静止。除了在氧化应激中的保护作用外,最近的一些进展表明Nrf2途径广泛参与癌症的发病机制,并赋予生存优势和恶性转化。因此,Nrf2的药理抑制是一种潜在的治疗与氧化应激和炎症相关的癌症的方法。本文首先介绍Nrf2的分子调控机制及其在肿瘤中的生物学功能。然后,我们讨论了阻断Nrf2活性的最新进展,包括新的化学分子,以及癌症治疗的临床前或临床试验的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting the Keap1/Nrf2 axis in cancer: molecular mechanisms and pharmacological interventions.

The transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) is the first-line regulator of a plethora of cytoprotective pathways, such as inflammation, redox metabolism, and proteostasis. Besides its protective role in oxidative stress, several recent advances suggested that the Nrf2 pathway is extensively involved in cancer pathogenesis and confers a survival advantage and malignant transformation. Therefore, pharmacological inhibition of Nrf2 is a potential therapeutic approach for cancer that is related to oxidative stress and inflammation. In this review, we first describe the molecular regulatory mechanisms of Nrf2 and its biological function in cancer. Then, we discuss the recent progress of blocking Nrf2 activity, comprising novel chemical molecules, and the advance in preclinical or clinical trials in cancer therapy.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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