Duckworth-Rysiecki G, Taylor A M
Cancer Res. 1985 Jan;45(1):416-20.
The lymphocytes from some Fanconi's anemia patients appeared to be more radiosensitive than normal as measured by the number of X-ray-(or bleomycin-) induced chromosome aberrations seen following G2 treatment. Fibroblasts from the same patients, however, all showed the same degree of colony survival as normals following exposure to gamma-rays [Do, 1.13 +/- 0.072 (S.E.) Gy and 1.14 +/- 0.077 Gy for Fanconi's anemia and normal fibroblasts, respectively]. The lack of increased radiosensitivity in Fanconi's fibroblasts was also observed by the same degree of inhibition of DNA synthesis as seen in normals following gamma-irradiation. The results show clearly that there is no increase in radiosensitivity common to all cell types from Fanconi's patients, although an apparent increase in chromosomal radiosensitivity may be seen in the lymphocytes from an occasional patient.
通过G2期处理后观察到的X射线(或博来霉素)诱导的染色体畸变数量来衡量,一些范可尼贫血患者的淋巴细胞似乎比正常人对辐射更敏感。然而,来自相同患者的成纤维细胞在暴露于γ射线后,其集落存活率与正常人相同[范可尼贫血和成纤维细胞的Do分别为1.13±0.072(标准误)Gy和1.14±0.077 Gy]。γ射线照射后,范可尼贫血成纤维细胞中DNA合成的抑制程度与正常人相同,这也表明其对辐射的敏感性没有增加。结果清楚地表明,范可尼贫血患者并非所有细胞类型的辐射敏感性都增加,尽管偶尔有患者的淋巴细胞可能会出现明显的染色体辐射敏感性增加。