Funasaka Y, Mishima Y, Ichihashi M, Sugiyama T
Department of Dermatology, Kobe University School of Medicine, Japan.
Dermatologica. 1988;177(4):200-11. doi: 10.1159/000248565.
We have established nonmetastatic mouse B16 melanoma clone, C1-2, and metastatic variant, C4-1, by subcloning the 30th passage of nonmetastatic W1-4 cells. We have investigated oncogene expression and chromosomal abnormalities to see whether there is some correlation with tumor progression and phenotypic diversification in melanoma cells. Not only metastatic C4-1 but also nonmetastatic C1-2 showed similarly high expression of c-Ha-ras and c-myc oncogenes by Northern blotting method. The chromosome numbers of both clones were distributed mainly within the range of 48-52. C1-2 had about 20 biarmed chromosomes and C4-1 had 13 or 14, which made real ploidy of C1-2 and C4-1, hypotetraploidy and triploidy, respectively. 21 marker chromosomes were commonly observed, while 9 marker chromosomes peculiar to C1-2 and 4 peculiar to C4-1 were constantly recognized. In partial accordance with a previous report, chromosomes 4, 5, 6, 8, 10, 13, 18, 19, and X were additionally observed in nonmetastatic C1-2 cells, compared with metastatic C4-1 cells. Furthermore, in our study, the increase of chromosomes 1, 15, and 16 was found to be greater in metastatic C4-1.
我们通过对非转移性W1-4细胞的第30代进行亚克隆,建立了非转移性小鼠B16黑色素瘤克隆C1-2和转移性变体C4-1。我们研究了癌基因表达和染色体异常,以观察它们是否与黑色素瘤细胞的肿瘤进展和表型多样化存在某种关联。通过Northern印迹法,转移性C4-1和非转移性C1-2均显示出相似的高表达的c-Ha-ras和c-myc癌基因。两个克隆的染色体数目主要分布在48-52范围内。C1-2有大约20条双臂染色体,C4-1有13或14条,这使得C1-2和C4-1的实际倍性分别为亚四倍体和三倍体。共观察到21条标记染色体,同时持续识别出9条C1-2特有的标记染色体和4条C4-1特有的标记染色体。与之前的报道部分一致,与转移性C4-1细胞相比,在非转移性C1-2细胞中额外观察到了染色体4、5、6、8、10、13、18、19和X。此外,在我们的研究中,发现转移性C4-1中染色体1、15和16的增加更为明显。