1] The Campbell Family Institute for Breast Cancer Research, University Health Network, 620 University Avenue, Toronto, Ontario M5G 2C1, Canada. [2].
Nat Rev Drug Discov. 2013 Dec;12(12):931-47. doi: 10.1038/nrd4002.
The regulation of oxidative stress is an important factor in both tumour development and responses to anticancer therapies. Many signalling pathways that are linked to tumorigenesis can also regulate the metabolism of reactive oxygen species (ROS) through direct or indirect mechanisms. High ROS levels are generally detrimental to cells, and the redox status of cancer cells usually differs from that of normal cells. Because of metabolic and signalling aberrations, cancer cells exhibit elevated ROS levels. The observation that this is balanced by an increased antioxidant capacity suggests that high ROS levels may constitute a barrier to tumorigenesis. However, ROS can also promote tumour formation by inducing DNA mutations and pro-oncogenic signalling pathways. These contradictory effects have important implications for potential anticancer strategies that aim to modulate levels of ROS. In this Review, we address the controversial role of ROS in tumour development and in responses to anticancer therapies, and elaborate on the idea that targeting the antioxidant capacity of tumour cells can have a positive therapeutic impact.
氧化应激的调节是肿瘤发生发展及其对癌症治疗反应的重要因素。许多与肿瘤发生相关的信号通路也可以通过直接或间接的机制来调节活性氧(ROS)的代谢。高水平的 ROS 通常对细胞有害,癌细胞的氧化还原状态通常与正常细胞不同。由于代谢和信号异常,癌细胞表现出升高的 ROS 水平。观察到这种情况通过增加抗氧化能力来平衡,这表明高 ROS 水平可能构成肿瘤发生的障碍。然而,ROS 也可以通过诱导 DNA 突变和致癌信号通路来促进肿瘤形成。这些矛盾的作用对旨在调节 ROS 水平的潜在抗癌策略具有重要意义。在这篇综述中,我们探讨了 ROS 在肿瘤发生发展及其对癌症治疗反应中的争议性作用,并详细阐述了靶向肿瘤细胞抗氧化能力可能产生积极治疗效果的观点。