Wilson George D
Department of Radiation Oncology, Barbara Ann Karmanos Cancer Institute, Hudson Webber Building, Room 816, 4100 John R, Wayne State University, Detroit, MI 48201-2013, USA.
Cancer Metastasis Rev. 2004 Aug-Dec;23(3-4):209-25. doi: 10.1023/B:CANC.0000031762.91306.b4.
The cell cycle has been inextricably linked to the cellular response to radiation for many years. However, it is only in the past decade that the concept of a coordinated DNA damage response integrating damage recognition, cell cycle checkpoints and DNA repair has begun to be elucidated. The ATM protein is emerging as a key orchestrator of the damage response activating a wide variety of effectors involved in cell cycle arrest and DNA repair to elicit a concerted effort to prevent genome instability caused by unwanted changes in DNA sequence. The key proteins involved in cell cycle checkpoints in different phases of the cell cycle, and their interaction, is a fertile and rapidly developing area of research. This review summarizes the current state of knowledge of cellular checkpoints in response to radiation-induced double-strand breaks in mammalian cells and how this impacts on radiosensitivity.
多年来,细胞周期一直与细胞对辐射的反应紧密相连。然而,直到过去十年,整合损伤识别、细胞周期检查点和DNA修复的协调DNA损伤反应概念才开始得到阐明。ATM蛋白正成为损伤反应的关键协调者,它激活多种参与细胞周期阻滞和DNA修复的效应器,共同努力防止由DNA序列意外变化导致的基因组不稳定。细胞周期不同阶段参与细胞周期检查点的关键蛋白及其相互作用,是一个活跃且快速发展的研究领域。本综述总结了哺乳动物细胞中对辐射诱导双链断裂的细胞检查点的当前知识状态,以及这如何影响放射敏感性。