McKinnon Peter J
Department of Genetics and Tumor Cell Biology, St Jude Children's Research Hospital, 332 N.Lauderdale, Memphis, Tennessee 38105, USA.
EMBO Rep. 2004 Aug;5(8):772-6. doi: 10.1038/sj.embor.7400210.
Ataxia telangiectasia (AT) has long intrigued the biomedical research community owing to the spectrum of defects that are characteristic of the disease, including neurodegeneration, immune dysfunction, radiosensitivity and cancer predisposition. Following the identification of mutations in ATM (ataxia telangiectasia, mutated) as the underlying cause of the disease, biochemical analysis of this protein kinase has shown that it is a crucial nexus for the cellular response to DNA double-stranded breaks. Many ATM kinase substrates are important players in the cellular responses that prevent cancer. Accordingly, AT is a disease that results from defects in the response to specific types of DNA damage. Thus, although it is a rare neurodegenerative disease, understanding the biology of AT will lead to a greater understanding of the fundamental processes that underpin cancer and neurodegeneration.
共济失调毛细血管扩张症(AT)长期以来一直吸引着生物医学研究界,因为该疾病具有一系列典型缺陷,包括神经退行性变、免疫功能障碍、放射敏感性和癌症易感性。在确定ATM(共济失调毛细血管扩张症突变基因)突变是该疾病的根本原因之后,对这种蛋白激酶的生化分析表明,它是细胞对DNA双链断裂反应的关键枢纽。许多ATM激酶底物在预防癌症的细胞反应中起着重要作用。因此,AT是一种由对特定类型DNA损伤反应缺陷导致的疾病。所以,尽管它是一种罕见的神经退行性疾病,但了解AT的生物学特性将有助于更深入地理解支撑癌症和神经退行性变的基本过程。