Shikata I, Maehara Y, Fujiyoshi T, Endo H
Oncology. 1987;44(3):192-8. doi: 10.1159/000226475.
We isolated a cDNA clone, pAH1005, originating from the 6.8-kilobases mRNA of the rat ascites hepatoma cell line, AH60C. The sequence was highly expressed in various tumor tissues and tumor lines in rats, mice and humans. In rats, the expression of the sequence was also observed in fetal liver of 7 and 10 days of gestation, to some extent in the regenerating liver, yet was sparse in normal adult tissues. Additionally, this expression was induced when adult rat hepatocytes in primary monolayer cultures proliferated by the addition of epidermal growth factor and insulin. Southern blot analysis showed no major gene amplification and rearrangement between DNAs from hepatoma and normal liver of the same species. In addition, in vitro nuclear transcription assay revealed that a genomic clone corresponding to the pAH1005 hybridized to the nascent RNA from isolated nuclei of AH60C but not from those of normal rat liver. All these observations suggest that the expression of the conserved sequence we isolated is closely associated with cell growth and is regulated at the transcriptional level.
我们从大鼠腹水肝癌细胞系AH60C的6.8千碱基mRNA中分离出一个cDNA克隆pAH1005。该序列在大鼠、小鼠和人类的各种肿瘤组织及肿瘤细胞系中高度表达。在大鼠中,该序列在妊娠7天和10天的胎肝中也有表达,在再生肝中有一定程度的表达,但在正常成年组织中表达稀少。此外,当原代单层培养的成年大鼠肝细胞通过添加表皮生长因子和胰岛素而增殖时,这种表达会被诱导。Southern印迹分析表明,同一物种肝癌组织和正常肝组织的DNA之间没有主要基因扩增和重排。另外,体外核转录分析显示,与pAH1005对应的基因组克隆与AH60C分离核的新生RNA杂交,但不与正常大鼠肝分离核的新生RNA杂交。所有这些观察结果表明,我们分离出的保守序列的表达与细胞生长密切相关,并在转录水平受到调控。