Aleksandrova S A, Shvemberger I N
Institute of Cytology, Russian Academy of Sciences, St. Petersburg.
Vopr Onkol. 2003;49(3):347-50.
The viability and genetic variability of mouse hepatoma MH-22a were studied by RAPD-PCR method using 3 primers, and the genetic structure of the tumor hepatocyte population based on the number of clonal fingerprint rearrangements was identified: 56% of hepatocytes made up clones with 0-3 rearrangements (the stem line of the population); 32%--the variable part with 4-7 rearrangements per clone and 12%--the aberrant part with 8-12 rearrangements per clone. The stem line appeared the most viable featuring zero or least genetic variability while the clones characterized by the greatest genetic variability were least viable.
采用随机扩增多态性DNA聚合酶链反应(RAPD-PCR)方法,使用3种引物研究了小鼠肝癌MH-22a的活力和遗传变异性,并根据克隆指纹重排数量确定了肿瘤肝细胞群体的遗传结构:56%的肝细胞构成了重排数为0至3的克隆(群体的主干系);32%为可变部分,每个克隆有4至7次重排;12%为异常部分,每个克隆有8至12次重排。主干系表现出最强的活力,遗传变异性为零或最小,而遗传变异性最大的克隆活力最低。