Dynamic Heterogeneity: Rapid Generation of Metastatic Variants in Mouse B16 Melanoma Cells
- 1 June 1984
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 224 (4652) , 998-1001
- https://doi.org/10.1126/science.6719130
Abstract
The ability of clonally derived lines of B16F1 and B16F10 melanoma cells to form experimental metastases in C57BL mice after intravenous injection was examined. Luria- Delbruck fluctuation analysis was applied to the results obtained with parallel subclones grown to small population sizes before testing for metastatic ability. The analysis demonstrated that variant cells capable of forming experimental metastases were generated in B16F1 cell populations at an effective rate of about 1.3 X 10(-5) per cell per generation while in B16F10 cell populations the effective rate of production was about 5 X 10(-5) per cell per generation. These results are consistent with a dynamic heterogeneity model of tumor progression. They suggest that the majority of cells in both lines are effectively nonmetastatic and that the higher metastatic ability of the B16F10 population may be due in part to a higher rate of generation of metastatic variants.This publication has 20 references indexed in Scilit:
- Modulation of the Metastatic Capability in B16 Melanoma by Cell ShapeScience, 1983
- CELLULAR ONCOGENES AND RETROVIRUSESAnnual Review of Biochemistry, 1983
- Tumor heterogeneity: biological implications and therapeutic consequencesCancer and Metastasis Reviews, 1983
- Biological Diversity in Metastatic Neoplasms: Origins and ImplicationsScience, 1982
- Metastatic variants are generated spontaneously at a high rate in mouse KHT tumor.Proceedings of the National Academy of Sciences, 1982
- Amplified DNA sequences in Y1 mouse adrenal tumor cells: association with double minutes and localization to a homogeneously staining chromosomal region.Proceedings of the National Academy of Sciences, 1982
- The role of gene dosage and genetic transpositions in carcinogenesisNature, 1981
- The Clonal Evolution of Tumor Cell PopulationsScience, 1976
- Capacity for tumor cell implantation as a function of in vitro cell densityBiochemical and Biophysical Research Communications, 1974
- Selection of Successive Tumour Lines for MetastasisNature New Biology, 1973