Schwab M, Varmus H E, Bishop J M
Nature. 1985;316(6024):160-2. doi: 10.1038/316160a0.
Proto-oncogenes represent a group of eukaryotic genes whose activated forms are implicated in the development of cancer. We have recently identified a human gene, N-myc, that is distantly related to the proto-oncogene c-myc. N-myc is expressed at abnormally high levels consequent to amplification in numerous human neuroblastoma cell lines and metastatic neuroblastoma tumours. In addition, enhanced expression of N-myc, often a result of amplification, has been found in retinoblastoma cell lines and tumours (refs 5, 7 and M.S., unpublished data) and in cell lines derived from small-cell carcinomas of the lung. Here, we show that enhanced expression of N-myc subsequent to co-transfections of an N-myc expression vector and the mutant c-Ha-ras-1(EJ) (from the human bladder carcinoma cell line EJ) is a factor in tumorigenic conversion of secondary rat embryo cells. The transformed cells elicit tumours in athymic mice and isogeneic rats. The ability of N-myc to contribute to neoplastic transformation of cultured mammalian cells raises the possibility that enhanced expression consequent to amplification of N-myc may be a factor in the aetiology of human neuroblastoma.
原癌基因是一组真核基因,其激活形式与癌症的发生发展有关。我们最近鉴定出一个人类基因N-myc,它与原癌基因c-myc有较远的亲缘关系。在众多人类神经母细胞瘤细胞系和转移性神经母细胞瘤肿瘤中,N-myc因扩增而异常高水平表达。此外,在视网膜母细胞瘤细胞系和肿瘤(参考文献5、7以及M.S.,未发表数据)以及源自肺小细胞癌的细胞系中,也发现了N-myc的表达增强,这通常是扩增的结果。在此,我们表明,在共转染N-myc表达载体和突变型c-Ha-ras-1(EJ)(来自人类膀胱癌细胞系EJ)后,N-myc表达增强是导致二代大鼠胚胎细胞致瘤转化的一个因素。转化后的细胞在无胸腺小鼠和同基因大鼠中引发肿瘤。N-myc促成培养的哺乳动物细胞发生肿瘤转化的能力,增加了N-myc扩增导致其表达增强可能是人类神经母细胞瘤病因的一个因素的可能性。