Cancer Research-UK Labs, Department of Surgery and Cancer, Imperial College London, Hammersmith Campus, London, England, United Kingdom.
Antioxid Redox Signal. 2011 Feb 15;14(4):675-87. doi: 10.1089/ars.2010.3383. Epub 2010 Oct 20.
Forkhead box O (FOXO) transcription factors are at the center of an emerging paradigm that links longevity, cell fate, and tumor development. Key to these processes is the ability of FOXO to regulate, and be regulated by, oxidative stress. Perturbation of the mechanisms that tightly couple reactive oxygen species (ROS) production, oxidative stress signaling, and FOXO activity to the subsequent cellular response is a pivotal step in cancer development and progression. Consequently, the ROS-FOXO pathway is a major therapeutic target in cancer, not only as it mediates the cellular response to chemotherapy, but also because it underpins drug resistance. As the intimate and reciprocal relation between FOXO and ROS is being unravelled, new opportunities arise to develop more-effective cancer treatments that circumvent resistance to the conventional cytotoxic drugs.
叉头框 O (FOXO) 转录因子是一个新兴范式的核心,该范式将长寿、细胞命运和肿瘤发展联系起来。这些过程的关键是 FOXO 调节和被氧化应激调节的能力。扰乱将活性氧 (ROS) 产生、氧化应激信号和 FOXO 活性紧密偶联到随后的细胞反应的机制,是癌症发展和进展的关键步骤。因此,ROS-FOXO 途径是癌症的主要治疗靶点,不仅因为它介导了细胞对化疗的反应,还因为它是耐药性的基础。随着 FOXO 和 ROS 之间的密切和相互关系的揭示,出现了开发更有效的癌症治疗方法的新机会,这些方法可以规避对传统细胞毒性药物的耐药性。