Kastan M B, Lim D S, Kim S T, Yang D
Department of Hematology-Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.
Acta Oncol. 2001;40(6):686-8. doi: 10.1080/02841860152619089.
Ataxia-telangiectasia is a rare clinical disorder manifesting a variety of different abnormalities, including progressive neurodegeneration, increased cancer incidence, immune deficiency, sterility, and extreme radiosensitivity. Recent studies have demonstrated that the defective gene product in this disease, ATM, is a protein kinase. The identification of several different substrates for this kinase is beginning to explain the wide array of different physiologic abnormalities that occur when this gene product is dysfunctional. Since the ATM protein is a critical signaling molecule in the cellular response to ionizing irradiation, the identification of these substrates also results in elucidation of the steps involved in a number of different cellular signaling pathways initiated by irradiation. Such insights also result in the identification of potential new targets for enhancing the efficacy of radiation therapy.
共济失调毛细血管扩张症是一种罕见的临床病症,表现出多种不同异常,包括进行性神经退行性变、癌症发病率增加、免疫缺陷、不育以及极高的放射敏感性。最近的研究表明,这种疾病中存在缺陷的基因产物ATM是一种蛋白激酶。对该激酶几种不同底物的鉴定,开始解释了当这种基因产物功能失调时所出现的一系列不同生理异常。由于ATM蛋白是细胞对电离辐射反应中的关键信号分子,这些底物的鉴定也有助于阐明由辐射引发的许多不同细胞信号通路所涉及的步骤。这些见解还促成了对提高放射治疗疗效潜在新靶点的鉴定。