Murray M J, Cunningham J M, Parada L F, Dautry F, Lebowitz P, Weinberg R A
Cell. 1983 Jul;33(3):749-57. doi: 10.1016/0092-8674(83)90017-x.
The oncogene of the HL-60 human promyelocytic leukemia cell line has been passed serially through NIH/3T3 mouse fibroblasts. Oncogene-specific probes prepared from the resulting tertiary transfectants by molecular cloning have been used to show that loss of the transfected oncogene from NIH/3T3 cells correlates with reversion to nontransformed morphology. Analysis of cells transfected by the oncogenes of other tumors and tumor cell lines indicates that the transforming gene of the HL-60 leukemia cell line is closely related to oncogenes of a Burkitt's lymphoma, an acute myelogenous leukemia, an adenocarcinoma of the colon, a neuroblastoma, and two sarcomas. This oncogene is distantly related to the viral oncogenes of Kirsten and Harvey sarcoma viruses. It has been termed N-ras. The active N-ras oncogene coexists with altered versions of the myc oncogene in the HL-60 and AW Ramos human tumors. This suggests a multistep mechanism involving both ras and myc genes in the creation of these tumors.
HL-60人早幼粒细胞白血病细胞系的癌基因已通过NIH/3T3小鼠成纤维细胞进行了连续传代。通过分子克隆从所得的三级转染子制备的癌基因特异性探针已用于表明NIH/3T3细胞中转染癌基因的丢失与向未转化形态的逆转相关。对由其他肿瘤和肿瘤细胞系的癌基因转染的细胞的分析表明,HL-60白血病细胞系的转化基因与伯基特淋巴瘤、急性髓性白血病、结肠腺癌、神经母细胞瘤和两种肉瘤的癌基因密切相关。该癌基因与柯斯顿和哈维肉瘤病毒的病毒癌基因有较远的关系。它被命名为N-ras。活性N-ras癌基因与HL-60和AW Ramos人肿瘤中myc癌基因的改变形式共存。这表明在这些肿瘤的发生过程中涉及ras和myc基因的多步骤机制。