Bravard A, Hoffschir F, Sabatier L, Ricoul M, Pinton A, Cassingena R, Estrade S, Luccioni C, Dutrillaux B
CEA/DSV/DPTE/LCG, Fontenay aux Roses, France.
Int J Cancer. 1992 Nov 11;52(5):797-801. doi: 10.1002/ijc.2910520521.
The expression of superoxide dismutases (SOD) 1 and 2 was studied in 4 clones of human fibroblasts after their infection by simian virus 40 (SV40), in parallel with the alterations of chromosomes 21 and chromosome 6q arms, carrying the genes that encode for SOD1 and SOD2 respectively. For all clones, a similar scheme with 2 main phases was observed for both chromosome and SOD variations. The first phase, defined as the pre-crisis phase, was characterized by chromosomal instability, but maintenance of normal numbers of chromosome 6q arms and chromosomes 21. The level of SOD2 mRNA was high, while SOD2 activity and immunoreactive protein were low. SOD1 protein and activity were decreased. In the second phase, defined as the post-crisis phase, the accumulation of clonal chromosomal rearrangements led to the loss of 6q arms, while the number of chromosomes 21 remained normal. SOD2 mRNA level was decreased and SOD2 immunoreactive protein and activity remained low. SOD1 protein and activity increased with passages, reaching values similar to those of control cells at late passages. As in established SV40-transformed human fibroblast cell lines, good correlation was found between SOD2 activity and the relative number of 6q arms. These results allow us to reconstruct the sequence of events leading to the decrease of SOD2, a possible tumor-suppressor gene, during the process of SV40-transformation of human fibroblasts.
在人成纤维细胞的4个克隆被猴病毒40(SV40)感染后,研究了超氧化物歧化酶(SOD)1和2的表达,并同时观察了分别携带编码SOD1和SOD2基因的21号染色体和6q染色体臂的变化。对于所有克隆,在染色体和SOD变异方面都观察到了一个有2个主要阶段的相似模式。第一阶段,定义为危机前阶段,其特征是染色体不稳定,但6q染色体臂和21号染色体的数量保持正常。SOD2 mRNA水平较高,而SOD2活性和免疫反应性蛋白水平较低。SOD1蛋白和活性降低。在第二阶段,定义为危机后阶段,克隆染色体重排的积累导致6q染色体臂丢失,而21号染色体的数量保持正常。SOD2 mRNA水平降低,SOD2免疫反应性蛋白和活性仍然较低。SOD1蛋白和活性随着传代次数增加,在传代后期达到与对照细胞相似的值。如同在已建立的SV40转化的人成纤维细胞系中一样,发现SOD2活性与6q染色体臂的相对数量之间存在良好的相关性。这些结果使我们能够重建在人成纤维细胞的SV40转化过程中导致可能的肿瘤抑制基因SOD2减少的一系列事件。