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FAM129B-dependent activation of NRF2 promotes an invasive phenotype in BRAF mutant melanoma cells.FAM129B 依赖性激活 NRF2 促进 BRAF 突变黑色素瘤细胞的侵袭表型。
Mol Carcinog. 2021 May;60(5):331-341. doi: 10.1002/mc.23295. Epub 2021 Mar 8.
2
Mild Oxidative Stress Reduces NRF2 SUMOylation to Promote // Mutant Lung Adenocarcinoma Cell Migration and Invasion.轻度氧化应激可减少 NRF2 的 SUMOylation 从而促进 // 突变型肺腺癌细胞的迁移和侵袭。
Oxid Med Cell Longev. 2020 Nov 24;2020:6240125. doi: 10.1155/2020/6240125. eCollection 2020.
3
Epigenetic Regulation of NRF2/KEAP1 by Phytochemicals.植物化学物质对NRF2/KEAP1的表观遗传调控
Antioxidants (Basel). 2020 Sep 14;9(9):865. doi: 10.3390/antiox9090865.
4
Activation of NRF2 by topical apocarotenoid treatment mitigates radiation-induced dermatitis.局部类胡萝卜素处理激活 NRF2 可减轻辐射诱导的皮炎。
Redox Biol. 2020 Oct;37:101714. doi: 10.1016/j.redox.2020.101714. Epub 2020 Sep 4.
5
Molecular Mechanisms Underlying Hepatocellular Carcinoma Induction by Aberrant NRF2 Activation-Mediated Transcription Networks: Interaction of NRF2-KEAP1 Controls the Fate of Hepatocarcinogenesis.异常 NRF2 激活介导的转录网络导致肝细胞癌发生的分子机制:NRF2-KEAP1 相互作用控制肝癌发生的命运。
Int J Mol Sci. 2020 Jul 29;21(15):5378. doi: 10.3390/ijms21155378.
6
Chronic arsenic exposure enhances metastatic potential via NRF2-mediated upregulation of SOX9.慢性砷暴露通过 NRF2 介导的 SOX9 上调增强转移潜能。
Toxicol Appl Pharmacol. 2020 Sep 1;402:115138. doi: 10.1016/j.taap.2020.115138. Epub 2020 Jul 17.
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Oxidative Stress in Cancer.癌症中的氧化应激。
Cancer Cell. 2020 Aug 10;38(2):167-197. doi: 10.1016/j.ccell.2020.06.001. Epub 2020 Jul 9.
8
Enhanced p62-NRF2 Feedback Loop due to Impaired Autophagic Flux Contributes to Arsenic-Induced Malignant Transformation of Human Keratinocytes.增强的 p62-NRF2 反馈环归因于自噬通量受损,导致人类角质形成细胞砷诱导的恶性转化。
Oxid Med Cell Longev. 2019 Oct 30;2019:1038932. doi: 10.1155/2019/1038932. eCollection 2019.
9
Regulation of Nrf2 Signaling.Nrf2信号通路的调控
React Oxyg Species (Apex). 2019 Nov;8(24):312-322.
10
A Comparative Assessment Study of Known Small-Molecule Keap1-Nrf2 Protein-Protein Interaction Inhibitors: Chemical Synthesis, Binding Properties, and Cellular Activity.已知小分子 Keap1-Nrf2 蛋白-蛋白相互作用抑制剂的比较评估研究:化学合成、结合特性和细胞活性。
J Med Chem. 2019 Sep 12;62(17):8028-8052. doi: 10.1021/acs.jmedchem.9b00723. Epub 2019 Aug 27.

NRF2 调控在癌症中的复杂性。

The intricacies of NRF2 regulation in cancer.

机构信息

Deparment of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA.

Deparment of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA; University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.

出版信息

Semin Cancer Biol. 2021 Nov;76:110-119. doi: 10.1016/j.semcancer.2021.05.016. Epub 2021 May 18.

DOI:10.1016/j.semcancer.2021.05.016
PMID:34020028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8599504/
Abstract

The complex role of NRF2 in the context of cancer continues to evolve. As a transcription factor, NRF2 regulates various genes involved in redox homeostasis, protein degradation, DNA repair, and xenobiotic metabolism. As such, NRF2 is critical in preserving cell function and viability, particularly during stress. Importantly, NRF2 itself is regulated via a variety of mechanisms, and the mode of NRF2 activation often dictates the duration of NRF2 signaling and its role in either preventing cancer initiation or promoting cancer progression. Herein, different modes of NRF2 regulation, including oxidative stress, autophagy dysfunction, protein-protein interactions, and epigenetics, as well as pharmacological modulators targeting this cascade in cancer, are explored. Specifically, how the timing and duration of these different mechanisms of NRF2 induction affect tumor initiation, progression, and metastasis are discussed. Additionally, progress in the discovery and development of NRF2 inhibitors for the treatment of NRF2-addicted cancers is highlighted, including modulators that inhibit specific NRF2 downstream targets. Overall, a better understanding of the intricate nature of NRF2 regulation in specific cancer contexts should facilitate the generation of novel therapeutics designed to not only prevent tumor initiation, but also halt progression and ultimately improve patient wellbeing and survival.

摘要

NRF2 在癌症中的复杂作用仍在不断发展。作为一种转录因子,NRF2 调节涉及氧化还原稳态、蛋白质降解、DNA 修复和外来物代谢的各种基因。因此,NRF2 对于维持细胞功能和活力至关重要,特别是在应激期间。重要的是,NRF2 本身通过多种机制进行调节,NRF2 的激活方式通常决定了 NRF2 信号的持续时间及其在预防癌症发生或促进癌症进展中的作用。本文探讨了 NRF2 调节的不同模式,包括氧化应激、自噬功能障碍、蛋白-蛋白相互作用和表观遗传学,以及针对癌症中这一级联反应的药理学调节剂。具体而言,讨论了这些不同的 NRF2 诱导机制的时间和持续时间如何影响肿瘤的起始、进展和转移。此外,还强调了发现和开发用于治疗 NRF2 成瘾性癌症的 NRF2 抑制剂的进展,包括抑制特定 NRF2 下游靶标的调节剂。总的来说,更好地了解 NRF2 在特定癌症环境中的复杂调节性质应有助于生成旨在不仅预防肿瘤起始,而且阻止进展并最终改善患者的健康状况和生存的新型治疗方法。