靶向NRF2及其下游过程:机遇与挑战。

IF 11.2 1区 医学 Q1 PHARMACOLOGY & PHARMACY Annual review of pharmacology and toxicology Pub Date : 2022-01-06 Epub Date: 2021-09-09 DOI:10.1146/annurev-pharmtox-052220-104025
Laura Torrente, Gina M DeNicola
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引用次数: 49

摘要

转录因子NRF2协调大量细胞保护和代谢基因的表达,以响应各种应激输入,恢复细胞稳态。长期以来,NRF2在健康组织中的瞬时激活一直被认为是一种细胞防御机制,对于防止致癌物引发癌症至关重要。然而,癌细胞经常劫持NRF2的保护能力来维持氧化还原平衡并满足其增殖的代谢需求。此外,癌细胞中NRF2的异常激活使其对常用的化疗药物和放疗产生耐药性。在过去的十年中,许多研究小组试图阻断NRF2在肿瘤中的活性,以抵消癌细胞的生存和增殖优势,并逆转对治疗的耐药性。在这篇综述中,我们强调了NRF2在癌症进展中的作用,并讨论了过去和现在在肿瘤中禁用NRF2信号的方法。
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Targeting NRF2 and Its Downstream Processes: Opportunities and Challenges.

The transcription factor NRF2 coordinates the expression of a vast array of cytoprotective and metabolic genes in response to various stress inputs to restore cellular homeostasis. Transient activation of NRF2 in healthy tissues has been long recognized as a cellular defense mechanism and is critical to prevent cancer initiation by carcinogens. However, cancer cells frequently hijack the protective capability of NRF2 to sustain the redox balance and meet their metabolic requirements for proliferation. Further, aberrant activation of NRF2 in cancer cells confers resistance to commonly used chemotherapeutic agents and radiotherapy. During the last decade, many research groups have attempted to block NRF2 activity in tumors to counteract the survival and proliferative advantage of cancer cells and reverse resistance to treatment. In this review, we highlight the role of NRF2 in cancer progression and discuss the past and current approaches to disable NRF2 signaling in tumors.

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来源期刊
CiteScore
27.80
自引率
0.00%
发文量
53
期刊介绍: Since 1961, the Annual Review of Pharmacology and Toxicology has been a comprehensive resource covering significant developments in pharmacology and toxicology. The journal encompasses various aspects, including receptors, transporters, enzymes, chemical agents, drug development science, and systems like the immune, nervous, gastrointestinal, cardiovascular, endocrine, and pulmonary systems. Special topics are also featured in this annual review.
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