Gebhart E, Neubauer S, Schmitt G, Birkenhake S, Dunst J
Institut für Humangenetik der Universität, Erlangen, Germany.
Radiat Res. 1996 Jan;145(1):47-52.
A three-color chromosome in situ suppression technique and classical cytogenetic analysis were compared for the detection of chromosomal aberrations in blood lymphocytes of 27 patients who had undergone radiation therapies from 1 month to 9 years ago. Depending on the respective regimens of therapy, a high variability was found in the aberration data. Aberration rates depended on the interval between exposure and scoring rather than on the locally applied radiation doses, which were rather uniform among most patients. Chromosome in situ suppression was found to be superior to classical cytogenetics with respect not only to the spectrum of detectable aberrations but also to the uncovering of long-term effects of irradiation. Of particular interest were the relative stability of the frequency of radiation-induced reciprocal translocations and the utility of chromosome in situ suppression to uncover complex rearrangements.
对27例在1个月至9年前接受过放射治疗的患者的血液淋巴细胞进行染色体畸变检测时,比较了三色染色体原位抑制技术和经典细胞遗传学分析。根据各自的治疗方案,在畸变数据中发现了高度变异性。畸变率取决于暴露与评分之间的间隔,而不是局部应用的辐射剂量,大多数患者的辐射剂量相当一致。发现染色体原位抑制不仅在可检测畸变的谱方面,而且在揭示辐射的长期效应方面都优于经典细胞遗传学。特别令人感兴趣的是辐射诱导的相互易位频率的相对稳定性以及染色体原位抑制在揭示复杂重排方面的效用。