Mendelsohn M L
Lawrence Livermore National Laboratory, Biomedical Sciences Division, Livermore, CA 94550.
Health Phys. 1990 Jul;59(1):23-8. doi: 10.1097/00004032-199007000-00002.
Methods for measuring somatic mutation and chromosome aberration in humans are currently advancing and provide important new opportunities for biologic dosimetry of nuclear workers. Methods to test somatic mutation in four human genes (hprt, hla-a, glycophorin A, and beta globin) are reviewed briefly and evaluated for their applicability to biological radiation dosimetry of nuclear workers. Two somatic mutation tests can be currently recommended: an HPRT method applied to recently exposed workers and the glycophorin A method applied to workers exposed over their working lifetime. A new method of chromosome analysis using DNA hybridization with chromosome-specific gene libraries allows one to paint single or multiple chromosome pairs in standard metaphase preparations. This method is ideal for rapid and reliable detection of reciprocal translocations, the key lesion for the evaluation of long-term radiation exposure. Both mutational and aberrational approaches should be fostered in the expectation that they will complement other forms of dosimetry and will improve our ability to clarify whether or not significant health effects are dosimetrically related.
目前,用于测量人体体细胞突变和染色体畸变的方法正在不断发展,为核工业工作者的生物剂量测定提供了重要的新机遇。本文简要回顾了检测人类四个基因(次黄嘌呤磷酸核糖转移酶、人类白细胞抗原A、血型糖蛋白A和β珠蛋白)中体细胞突变的方法,并对其在核工业工作者生物辐射剂量测定中的适用性进行了评估。目前可以推荐两种体细胞突变检测方法:一种是应用于近期受照工作者的次黄嘌呤磷酸核糖转移酶方法,另一种是应用于整个工作期间受照工作者的血型糖蛋白A方法。一种利用与染色体特异性基因文库进行DNA杂交的染色体分析新方法,能够在标准中期制备物中对单条或多条染色体对进行染色。该方法非常适合快速、可靠地检测相互易位,这是评估长期辐射暴露的关键损伤。应同时推动突变检测和畸变检测方法的发展,以期它们能与其他剂量测定形式相互补充,并提高我们明确重大健康效应是否与剂量相关的能力。