Introduction of metastatic heterogeneity by short‐term in vivo passage of a cloned transformed cell line

作者：James E. Talmadge, Jean R. Starkey, William C. Davis, Arthur L. Cohen · 发表于：Journal of Supramolecular Structure · 年份：1979 · DOI：10.1002/jss.400120208 · 被引用次数：53 · 研究领域：Cancer Genomics and Diagnostics、Cancer Cells and Metastasis、Cancer Research and Treatments

An experimental system for the study of metastasis has been developed using an epithelioid cell line of hepatic origin which had previously been chemically transformed in vitro. These metastatic cells were studied in the syngeneic rat strain. The cloned parent cell line metastasizes only to the lungs following intravenous, subcutaneous, or intraperitoneal injection. The metastatic phenotype is stable during in vitro passage, and subclones from the parent clone have a metastatic capacity statistically similar to that of the parent clone. Following ascites passage of the parent cell line, the cell population obtained exhibits the same metastatic ability as the parent clone. However, subclones obtained from the ascites-passaged population exhibit metastatic heterogeneity. This heterogeneity is introduced by the host passage and not by in vitro culture or subcloning. In the case of the two metastatic variants examined, the difference in the metastatic phenotype is found not to be due to differences in arrest or trapping of the cells but appears to be related to long-term survival and proliferation of the tumor cells following their arrest in the lungs. Morphologically the variants are very similar, and growth of the metastatic foci provokes a vigorous inflammatory response by the host.