Trachootham Dunyaporn, Alexandre Jerome, Huang Peng
Department of Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Nat Rev Drug Discov. 2009 Jul;8(7):579-91. doi: 10.1038/nrd2803. Epub 2009 May 29.
Increased generation of reactive oxygen species (ROS) and an altered redox status have long been observed in cancer cells, and recent studies suggest that this biochemical property of cancer cells can be exploited for therapeutic benefits. Cancer cells in advanced stage tumours frequently exhibit multiple genetic alterations and high oxidative stress, suggesting that it might be possible to preferentially eliminate these cells by pharmacological ROS insults. However, the upregulation of antioxidant capacity in adaptation to intrinsic oxidative stress in cancer cells can confer drug resistance. Abrogation of such drug-resistant mechanisms by redox modulation could have significant therapeutic implications. We argue that modulating the unique redox regulatory mechanisms of cancer cells might be an effective strategy to eliminate these cells.
长期以来,人们在癌细胞中观察到活性氧(ROS)生成增加以及氧化还原状态改变,最近的研究表明,癌细胞的这种生化特性可用于治疗目的。晚期肿瘤中的癌细胞经常表现出多种基因改变和高氧化应激,这表明通过药理学ROS损伤可能优先消除这些细胞。然而,癌细胞为适应内在氧化应激而上调抗氧化能力可导致耐药性。通过氧化还原调节消除此类耐药机制可能具有重大治疗意义。我们认为,调节癌细胞独特的氧化还原调节机制可能是消除这些细胞的有效策略。