Pathak S, Staroselsky A N, Fidler I J
Department of Cell Biology, University of Texas M. D. Anderson Cancer Center, Houston.
Cancer Genet Cytogenet. 1991 Oct 15;56(2):209-21. doi: 10.1016/0165-4608(91)90173-r.
In this study we sought to identify specific cytogenetic defects associated with the metastatic phenotypes in clones isolated from the parental K-1735 murine melanoma. All nonmetastatic clones (C-3, C-10, and C-19) exhibited trisomy of chromosomes 1, 3, 12, and 15. The only structural defect present in these clones was an interstitial deletion in a chromosome 4. In contrast, the highly metastatic clones (C-4, M-2, BB1, and X-21) exhibited trisomy of chromosomes 1, 3, 12, and 15, plus structural abnormalities of chromosomes 4 and 14, with the net result of a deletion in both. Parental K-1735 cells and clone C-16 cells, which are intermediate in their metastatic potential, had some cells with 4 and 14 alterations and others with only a deletion of chromosome 4. Clone C-16 revealed other non-clonal structural abnormalities. Our results indicate that structural anomaly of chromosome 4 and numerical alterations of certain autosomes may be associated with tumorigenic properties. In addition, structural defect in chromosome 14 is associated with high metastatic potential of K-1735 melanoma cells.
在本研究中,我们试图鉴定与从亲本K - 1735小鼠黑色素瘤分离出的克隆中的转移表型相关的特定细胞遗传学缺陷。所有非转移性克隆(C - 3、C - 10和C - 19)均表现出染色体1、3、12和15三体性。这些克隆中存在的唯一结构缺陷是4号染色体的中间缺失。相比之下,高转移性克隆(C - 4、M - 2、BB1和X - 21)表现出染色体1、3、12和15三体性,以及4号和14号染色体的结构异常,最终结果是两者均有缺失。亲本K - 1735细胞和转移潜能处于中间水平的克隆C - 16细胞,一些细胞有4号和14号染色体改变,另一些细胞只有4号染色体缺失。克隆C - 16还显示出其他非克隆性结构异常。我们的结果表明,4号染色体的结构异常和某些常染色体的数目改变可能与致瘤特性有关。此外,14号染色体的结构缺陷与K - 1735黑色素瘤细胞的高转移潜能有关。