Metastatic Murine and Human Neoplasms Gene in Clonal Populations

The purpose of this study was to determine whether nm23 steadystate mRNA expression levels correlate with metastatic potential of mouse K-1735 melanoma cells, human KM 12 colon cancer cells, and human SN12 renal cancer cells. Since neoplasms are heterogeneous and contain subpopulations of cells with different metastatic potentials, we analyzed multiple sets of nonmetastatic and metastatic clones isolated from each neoplasm. In addition, we also examined nine somatic cell hybrids produced by the fusion of nonmetastatic and metastatic K-1735 clones. In the mouse melanoma, we found heterogeneity in nm23-l steady-state expression levels among the clones and hybrids that did not correlate with their metastatic phenotype. Clones isolated from human colon or renal carcinomas expressed similar levels of nm23-HI regard less of metastatic potential in nude mice. All of the human tumor cells were heterozygous for the nm^J-///-$pecific allelic DNA fragments, with no allelic deletions or gross alterations detected. Since the failure of tumor cells to produce metastasis can be due to multiple deficiencies, these data stress the importance of using independent clones with dif ferent metastatic potentials for the analysis of gene regulation of this process.