Steeg P S
Laboratory of Pathology, National Cancer Institute, Bethesda, Md.
Invasion Metastasis. 1989;9(6):351-9.
Cell fusion experiments have predicted the existence of cancer metastasis suppressor genes. The E1a gene of Adenovirus 2 has been demonstrated to suppress c-Ha-ras induction of experimental metastatic potential in rat embryo fibroblasts. Another approach to the identification of candidate metastasis suppressor genes has utilized differential or subtraction hybridizations to clone genes which are downregulated as cells become highly metastatic. To date, three such genes have been identified: nm23, WDNM1, and fibronectin. With regard to nm23, downregulation of nm23 RNA levels in high metastatic potential cells has been demonstrated in a wide variety of rodent metastasis systems, including K-1735 murine melanoma cell lines, nitrosomethylurea-induced rat mammary tumors, MMTV-induced mouse mammary tumors, and ras +/- E1a transfected rat embryo fibroblasts. Whether the expression of the nm23 gene, and other down-regulated genes in tumor metastasis, correlates with changes in metastatic potential, or actually has suppressive activity, will require transfection experiments.
细胞融合实验预测了癌症转移抑制基因的存在。腺病毒2的E1a基因已被证明可抑制大鼠胚胎成纤维细胞中c-Ha-ras诱导的实验性转移潜能。另一种鉴定候选转移抑制基因的方法是利用差异杂交或消减杂交来克隆随着细胞变得高度转移而下调的基因。迄今为止,已鉴定出三个这样的基因:nm23、WDNM1和纤连蛋白。关于nm23,在多种啮齿动物转移系统中,包括K-1735小鼠黑色素瘤细胞系、亚硝基甲基脲诱导的大鼠乳腺肿瘤、MMTV诱导的小鼠乳腺肿瘤以及ras+/-E1a转染的大鼠胚胎成纤维细胞中,已证明高转移潜能细胞中nm23 RNA水平下调。nm23基因以及肿瘤转移中其他下调基因的表达是否与转移潜能的变化相关,或者实际上是否具有抑制活性,将需要进行转染实验。