Jenkins Tabitha, Gouge Jerome
Institute of Structural and Molecular Biology, Birkbeck College, University of London, London WC1E 7HX, UK.
Antioxidants (Basel). 2021 Jun 25;10(7):1030. doi: 10.3390/antiox10071030.
Reactive oxygen species (ROS) play an important role in cell proliferation and differentiation. They are also by-products of aerobic living conditions. Their inherent reactivity poses a threat for all cellular components. Cells have, therefore, evolved complex pathways to sense and maintain the redox balance. Among them, Nrf2 (Nuclear factor erythroid 2-related factor 2) plays a crucial role: it is activated under oxidative conditions and is responsible for the expression of the detoxification machinery and antiapoptotic factors. It is, however, a double edge sword: whilst it prevents tumorigenesis in healthy cells, its constitutive activation in cancer promotes tumour growth and metastasis. In addition, recent data have highlighted the importance of Nrf2 in evading programmed cell death. In this review, we will focus on the activation of the Nrf2 pathway in the cytoplasm, the molecular basis underlying Nrf2 binding to the DNA, and the dysregulation of this pathway in cancer, before discussing how Nrf2 contributes to the prevention of apoptosis and ferroptosis in cancer and how it is likely to be linked to detoxifying enzymes containing selenium.
活性氧(ROS)在细胞增殖和分化中发挥着重要作用。它们也是有氧生活条件下的副产物。其固有的反应活性对所有细胞成分构成威胁。因此,细胞进化出了复杂的途径来感知和维持氧化还原平衡。其中,Nrf2(核因子红细胞2相关因子2)起着关键作用:它在氧化条件下被激活,并负责解毒机制和抗凋亡因子的表达。然而,它是一把双刃剑:虽然它能防止健康细胞发生肿瘤发生,但其在癌症中的组成性激活会促进肿瘤生长和转移。此外,最近的数据突出了Nrf2在逃避程序性细胞死亡中的重要性。在这篇综述中,我们将重点关注细胞质中Nrf2途径的激活、Nrf2与DNA结合的分子基础以及该途径在癌症中的失调,然后讨论Nrf2如何有助于预防癌症中的细胞凋亡和铁死亡,以及它可能如何与含硒解毒酶相关联。