Muschel R J
Department of Pathology, University of Pennsylvania, Philadelphia 19104.
Cancer Res. 1990 Sep 1;50(17):5581-6.
The ras oncogene has been shown to induce metastatic potential in a wide variety of cells. However, one cell line, C127, when transformed by ras (HC127), proved to be an exception in that the transformed cells gained the ability to form tumors in nude mice, but these tumors did not form spontaneous metastases. Because C127 cells do not metastasize after ras transfection, these cells can be used to identify other factors which contribute to the development of metastatic potential. Specifically, these cells can be used as recipients in DNA transfer experiments utilizing DNA from other cells in which H-ras has been used to induce the metastatic phenotype, thus allowing the search for genes in addition to ras itself which may be necessary for metastasis. A system utilizing genomic DNA transfer into C127 cells transformed by ras has been developed. These cells were used as the recipient for genomic DNA in cotransfection with pSV2neo followed by selection both in the experimental i.v. assay and in the spontaneous metastasis assay in nude mice. DNA from two lines with metastatic potential (both transformed by ras genes) gave rise to metastatic clones, whereas DNA from the recipient cells, HC127, NIH 3T3 cells, and two human tumor cell lines, CHP126 and A2058, failed to give rise to transfectants which could metastasize. The metastases after the first cycle were put into culture, and DNA was extracted from these cells and used in a second cycle of transfection. The capacity to metastasize was also transferred in the second cycle. Of seven metastatic clones examined, four showed no detectable rearrangements of the transfected v-H-ras gene, but in three of these clones, there were rearrangements of this gene, which was originally present in the recipient cell, HC127. This indicates that in a subset of the selected clones there may have been selection for rearrangements of the host genome rather than introduction of foreign DNA sequences, and that such effects must be considered in gene transfer experiments. It is also possible that the transfer of particular genomic DNAs are leading to genetic instability in these experiments. mRNA levels were compared in the metastatic variants and the parental cells; H-ras-specific RNA was raised from 4- to 22-fold in the metastatic cell lines, regardless of rearrangement of the v-H-ras gene.
ras癌基因已被证明能在多种细胞中诱导转移潜能。然而,有一种细胞系C127,当被ras基因转化(HC127)后,却成为了一个例外,即转化后的细胞获得了在裸鼠体内形成肿瘤的能力,但这些肿瘤并不会自发转移。由于C127细胞在ras转染后不会转移,因此这些细胞可用于鉴定其他有助于转移潜能发展的因素。具体而言,这些细胞可作为DNA转移实验的受体,利用来自其他细胞的DNA,在这些细胞中H-ras已被用于诱导转移表型,从而能够寻找除ras自身之外可能对转移必不可少的基因。一种利用基因组DNA转移到被ras转化的C127细胞中的系统已被开发出来。这些细胞在与pSV2neo共转染时用作基因组DNA的受体,随后在实验性静脉注射试验和裸鼠自发转移试验中进行筛选。来自两个具有转移潜能的细胞系(均由ras基因转化)的DNA产生了转移克隆,而来自受体细胞HC127、NIH 3T3细胞以及两个人类肿瘤细胞系CHP126和A2058的DNA未能产生能够转移的转染子。将第一轮转移后的细胞进行培养,从这些细胞中提取DNA并用于第二轮转染。转移能力在第二轮中也得以传递。在检测的七个转移克隆中,四个未检测到转染的v-H-ras基因重排,但在其中三个克隆中,存在该基因的重排,该基因最初存在于受体细胞HC127中。这表明在一部分选定的克隆中,可能是对宿主基因组重排进行了选择,而非引入了外源DNA序列,并且在基因转移实验中必须考虑到这种影响。在这些实验中,特定基因组DNA的转移也有可能导致遗传不稳定。对转移变体和亲本细胞中的mRNA水平进行了比较;无论v-H-ras基因是否重排,转移细胞系中H-ras特异性RNA升高了4至22倍。