Alitalo K, Schwab M, Lin C C, Varmus H E, Bishop J M
Proc Natl Acad Sci U S A. 1983 Mar;80(6):1707-11. doi: 10.1073/pnas.80.6.1707.
Two human neuroendocrine tumor cell lines derived from a colon carcinoma contain either numerous double minute chromosomes (COLO 320 DM) or a homogeneously staining marker chromosome (COLO 320 HSR). We found amplification and enhanced expression of the cellular oncogene c-myc in both COLO 320 DM and HSR cells, and we were able to show that the homogeneously staining regions of the COLO 320 HSR marker chromosome contain amplified c-myc. From previous and present karyotypes, it appears that the homogeneously staining regions reside on a distorted X chromosome. Therefore, amplification of c-myc has been accompanied by translocation of the gene from its normal position on chromosome 8 (8q24). Because double minute chromosomes were features of primary cultures from the original tumor, it seems reasonable to suspect that amplification of c-myc may have contributed to tumorigenesis.
源自结肠癌的两个人类神经内分泌肿瘤细胞系,一个含有大量双微体染色体(COLO 320 DM),另一个含有一条均匀染色的标记染色体(COLO 320 HSR)。我们发现细胞癌基因c-myc在COLO 320 DM和HSR细胞中均有扩增和表达增强,并且我们能够证明COLO 320 HSR标记染色体的均匀染色区域含有扩增的c-myc。从既往和目前的核型来看,均匀染色区域似乎位于一条畸变的X染色体上。因此,c-myc的扩增伴随着该基因从其在8号染色体(8q24)上的正常位置发生易位。由于双微体染色体是原始肿瘤原代培养物的特征,所以怀疑c-myc的扩增可能促成了肿瘤发生似乎是合理的。