Lavin Martin F
Radiation Biology and Oncology Laboratory, Queensland Institute of Medical Research, Brisbane, QLD 4029, Australia.
Nat Rev Mol Cell Biol. 2008 Oct;9(10):759-69. doi: 10.1038/nrm2514.
First described over 80 years ago, ataxia-telangiectasia (A-T) was defined as a clinical entity 50 years ago. Although not encountered by most clinicians, it is a paradigm for cancer predisposition and neurodegenerative disorders and has a central role in our understanding of the DNA-damage response, signal transduction and cell-cycle control. The discovery of the protein A-T mutated (ATM) that is deficient in A-T paved the way for rapid progress on understanding how ATM functions with a host of other proteins to protect against genome instability and reduce the risk of cancer and other pathologies.
共济失调毛细血管扩张症(A-T)在80多年前首次被描述,50年前被定义为一种临床实体。尽管大多数临床医生并未遇到过这种疾病,但它是癌症易感性和神经退行性疾病的范例,在我们对DNA损伤反应、信号转导和细胞周期控制的理解中起着核心作用。A-T中缺失的蛋白质——共济失调毛细血管扩张症突变蛋白(ATM)的发现,为快速深入了解ATM如何与许多其他蛋白质协同作用以防止基因组不稳定、降低癌症和其他疾病风险铺平了道路。