Scudiero D A
Cancer Res. 1980 Apr;40(4):984-90.
DNA repair synthesis and posttreatment colony-forming ability were measured in six human fibroblast cell strains derived from patients with the autosomal recessive disorder, ataxia telangiectasia (AT), and five cell strains from normal individuals. All 11 cell strains showed approximately equal levels of DNA repair synthesis after methyl methanesulfonate and ultraviolet light treatments assayed by the benzoylated naphthoylated diethylaminoethyl-cellulose method. Four AT cell strains exhibited 27 to 41% of the repair shown by normal cell strains after treatment with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Two AT cell strains had normal levels of repair synthesis after MNNG treatment. All the AT strains tested had normal survival after treatment with methyl methanesulfonate and ultraviolet light as assayed by posttreatment colony-forming ability. The six AT cell strains exhibited diminished survival after MNNG treatment. The inhibition of [3H]thymidine uptake as a function of MNNG concentration was similar for all the normal and AT cell strains tested.
对来自常染色体隐性疾病共济失调毛细血管扩张症(AT)患者的6株人成纤维细胞系和5株正常个体的细胞系进行了DNA修复合成及处理后集落形成能力的检测。通过苯甲酰化萘甲酰化二乙氨基乙基纤维素法检测发现,所有11株细胞系在甲磺酸甲酯和紫外线处理后的DNA修复合成水平大致相当。在用N-甲基-N'-硝基-N-亚硝基胍(MNNG)处理后,4株AT细胞系的修复水平为正常细胞系的27%至41%。2株AT细胞系在MNNG处理后的修复合成水平正常。通过处理后集落形成能力检测发现,所有检测的AT细胞系在甲磺酸甲酯和紫外线处理后的存活率正常。6株AT细胞系在MNNG处理后的存活率降低。对于所有检测的正常和AT细胞系,[3H]胸腺嘧啶核苷摄取的抑制作为MNNG浓度的函数是相似的。