Kniazev P G, Schafer R, Willecke K, Pluzhnikova G F, Serova O M
Mol Biol (Mosk). 1986 Sep-Oct;20(5):1236-43.
DNA from human breast carcinoma (SK-BR-3) and neuroblastoma (LA-N-1) cell lines are capable of inducing foci of transformed NIH 3T3 cells after DNA-mediated gene transfer. The blot hybridization analysis of DNA from primary and secondary NIH 3T3 transformants identified additional sequences homologous to the c-Ha-ras 1 oncogene, and revealed amplification of nucleotide sequences homologous to the v-myc oncogene. Restriction fragments of the amplified myc-related sequences correspond to c-myc (SK-BR-3) and N-myc (LA-N-1) loci of the human genome. The results show that active Ha-ras oncogenes can coexist with altered myc oncogenes in breast carcinomas and neuroblastomas. This suggests that a multi-step mechanism involves both ras and myc genes and their cooperation in the development of these tumors.
人乳腺癌(SK-BR-3)和神经母细胞瘤(LA-N-1)细胞系的DNA在DNA介导的基因转移后能够诱导NIH 3T3转化细胞形成集落。对原代和二代NIH 3T3转化体的DNA进行印迹杂交分析,鉴定出与c-Ha-ras 1癌基因同源的其他序列,并揭示了与v-myc癌基因同源的核苷酸序列的扩增。扩增的myc相关序列的限制性片段对应于人类基因组的c-myc(SK-BR-3)和N-myc(LA-N-1)位点。结果表明,活性Ha-ras癌基因可与乳腺癌和神经母细胞瘤中改变的myc癌基因共存。这表明多步骤机制涉及ras和myc基因及其在这些肿瘤发生发展中的协同作用。