Eggler Aimee L, Savinov Sergey N
Department of Chemistry, Villanova University, 215a Mendel Science Hall, 800 Lancaster Avenue, Villanova, PA 19085.
Purdue University Center for Cancer Research, West Lafayette, Indiana, 47907.
Recent Adv Phytochem. 2013;43:121-155. doi: 10.1007/978-3-319-00581-2_7. Epub 2013 Dec 3.
Plants are an incredibly rich source of compounds that activate the Nrf2 transcription factor, leading to upregulation of a battery of cytoprotective genes. This perspective surveys established and proposed molecular mechanisms of Nrf2 activation by phytochemicals with a special emphasis on a common chemical property of Nrf2 activators: the ability as "soft" electrophiles to modify cellular thiols, either directly or as oxidized biotransformants. In addition, the role of reactive oxygen/nitrogen species as secondary messengers in Nrf2 activation is discussed. While the uniquely reactive C151 of Keap1, an Nrf2 repressor protein, is highlighted as a key target of cytoprotective phytochemicals, also reviewed are other stress-responsive proteins, including kinases, which play non-redundant roles in the activation of Nrf2 by plant-derived agents. Finally, the perspective presents two key factors accounting for the enhanced therapeutic windows of effective phytochemical activators of the Keap1-Nrf2 axis: enhanced selectivity toward sensor cysteines and reversibility of addition to thiolate molecules.
植物是激活Nrf2转录因子的化合物的极其丰富的来源,这会导致一系列细胞保护基因的上调。本文综述了已确立的和提出的植物化学物质激活Nrf2的分子机制,特别强调了Nrf2激活剂的一种常见化学性质:作为“软”亲电试剂直接或作为氧化生物转化产物修饰细胞硫醇的能力。此外,还讨论了活性氧/氮物种作为Nrf2激活中的二级信使的作用。虽然Nrf2阻遏蛋白Keap1独特的反应性C151被强调为细胞保护植物化学物质的关键靶点,但也综述了其他应激反应蛋白,包括激酶,它们在植物衍生剂激活Nrf2中发挥非冗余作用。最后,本文提出了两个关键因素,解释了Keap1-Nrf2轴有效植物化学激活剂治疗窗口扩大的原因:对传感器半胱氨酸的选择性增强以及与硫醇盐分子加成的可逆性。