Shaposhnikov Ia D, Kiselev O I, Gaĭtskhoki V S
Vopr Onkol. 1975;21(12):38-45.
The work was undertaken to estimate quantitatively the functional activity of tumor cell genome and possible variations in the relationship between nuclear genome and mitochondrial genetic determinants in tumor cell. For this purpose in mice C3HA tumors of hepatocellular origin were induced with N-nitroso-N-diethylamine, tissues of one of which were subjected to successive isologous transplantation during the period over 3 years. Normal hepatic tissues were taken for the control. As a result of a series of independent experiments (actinomycin D spectrophotometric titration, acridine orange binding, template activity, nuclear RNA/DNA hybridization) the results were obtained indicating a decrease in the amount of active loci in tumor hepatocytes genome. Hybridization data also indicate that in the tumor the derepression of chromosomal genes responsible for the genetic control over mitochondria and a non-regulated de-repression of mitochondrial genetic determinants take place.
开展这项工作是为了定量评估肿瘤细胞基因组的功能活性以及肿瘤细胞核基因组与线粒体遗传决定因素之间关系的可能变化。为此,用N-亚硝基-N-二乙胺诱导C3HA小鼠产生肝细胞源性肿瘤,其中一组肿瘤组织在3年多的时间里进行了连续的同系移植。取正常肝组织作为对照。通过一系列独立实验(放线菌素D分光光度滴定、吖啶橙结合、模板活性、核RNA/DNA杂交),结果表明肿瘤肝细胞基因组中活性位点的数量减少。杂交数据还表明,在肿瘤中,负责线粒体遗传控制的染色体基因去抑制以及线粒体遗传决定因素的非调节性去抑制发生。