Nemeth M A, Wilson M R, Fidler I J, Pathak S
Department of Cell Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Cancer Genet Cytogenet. 1997 Oct 15;98(2):119-25. doi: 10.1016/s0165-4608(96)00421-9.
The purpose of these studies was to demonstrate causal effects of abnormalities induced in mouse chromosome 14 on tumorigenicity and metastasis using the K-1735 murine melanoma cell line. Because anomalies in chromosome 14 have previously been associated with increases in metastatic potential, we induced chromosome 14 anomalies in a nonmetastatic K-1735 clone 10 cells initially containing two normal copies of chromosome 14 by treatment with mitomycin C. Clone 10-M1, in which a small population of cells (approximately 4%) contained translocations involving chromosome 14, was isolated and injected into athymic nude mice. Unlike the parental C-10 cells, C-10 M1 cells produced experimental lung metastases. Chromosomal analysis of cell cultures established from both subcutaneous tumors and lung metastases indicated that approximately 35% of the cell population contained chromosome 14 anomalies suggesting that this chromosome may play a role in tumor growth and metastasis.
这些研究的目的是利用K-1735小鼠黑色素瘤细胞系,证明小鼠14号染色体诱导的异常对肿瘤发生和转移的因果效应。由于先前已发现14号染色体异常与转移潜能增加有关,我们通过丝裂霉素C处理,在最初含有两个正常14号染色体拷贝的非转移性K-1735克隆10细胞中诱导14号染色体异常。分离出克隆10-M1,其中一小部分细胞(约4%)含有涉及14号染色体的易位,并将其注射到无胸腺裸鼠体内。与亲代C-10细胞不同,C-10 M1细胞产生了实验性肺转移。对皮下肿瘤和肺转移灶建立的细胞培养物进行染色体分析表明,约35%的细胞群体含有14号染色体异常,这表明该染色体可能在肿瘤生长和转移中起作用。