Evidence that intravenously derived murine pulmonary melanoma metastases can originate from the expansion of a single tumor cell.

The purpose of these studies was to determine whether hematogenous clonal pulmonary melanoma metastases originate from the expansion of a single cell and if so, by extrapolation, metastasis can be considered a cloning process. Three different cell lines of murine K-1735 melanoma with different metastatic properties and unique karyotypes were injected i.v. into syngeneic C3H/HeN mice as multicell aggregates of individual cell lines or combinations of cell lines. Resultant solitary lung metastases were isolated in culture as individual lines and then karyotyped. Even when heterogeneous clumps of tumor cells were injected, the individual metastases exhibited a karyotype unique to one metastatic cell type. Furthermore, when cellular aggregates were composed of metastatic cells admixed with cells that were tumorigenic but nonmetastatic, the resultant metastases exhibited only the karyotype of the metastatic cells. This finding suggests that the presence of metastatic cells did not change the inability of nonmetastatic cells to proliferate in a distant organ. Collectively, the results indicate that the resultant metastases were of clonal origin owing to the expansion of a single metastatic tumor cell in the lung parenchyma.

[1]  I. Fidler,et al.  Development of biological diversity and susceptibility to chemotherapy in murine cancer metastases. , 1984, Cancer research.

[2]  I. Fidler,et al.  The cellular heterogeneity of malignant neoplasms: implications for adjuvant chemotherapy. , 1985, Seminars in oncology.

[3]  L. Foulds The experimental study of tumor progression: a review. , 1954, Cancer research.

[4]  I. Fidler,et al.  Enhanced metastatic potential of tumor cells harvested from spontaneous metastases of heterogeneous murine tumors. , 1982, Journal of the National Cancer Institute.

[5]  I. Fidler,et al.  Metastasis: Quantitative Analysis of Distribution and Fate of Tumor Emboli Labeled With 125I-5-Iodo-2′ -deoxyuridine , 1970 .

[6]  I. Fidler,et al.  The pathogenesis of cancer metastasis , 1980, Nature.

[7]  J. Till,et al.  Cytological Demonstration of the Clonal Nature of Spleen Colonies Derived from Transplanted Mouse Marrow Cells , 1963, Nature.

[8]  G. Poste,et al.  Comparison of the metastatic properties of B16 melanoma clones isolated from cultured cell lines, subcutaneous tumors, and individual lung metastases. , 1982, Cancer research.

[9]  J E Talmadge,et al.  Evidence for the clonal origin of spontaneous metastases. , 1982, Science.

[10]  I. Fidler,et al.  Increasing metastatic potential is associated with increasing genetic instability of clones isolated from murine neoplasms. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[11]  I. Fidler,et al.  Metastasis results from preexisting variant cells within a malignant tumor. , 1977, Science.

[12]  I. Fidler,et al.  Biological and experimental consequences of the zonal composition of solid tumors. , 1981, Cancer research.

[13]  I. Fidler,et al.  Development and progression of karyotypic variability in melanoma K1735 following X-irradiation. , 1985, Cancer research.

[14]  R. Lotan,et al.  Low colony formation in vivo and in culture as exhibited by metastatic melanoma cells selected for reduced homotypic aggregation. , 1983, Cancer research.

[15]  G Poste,et al.  Evolution of tumor cell heterogeneity during progressive growth of individual lung metastases. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[16]  I. Fidler,et al.  Cancer metastasis is selective or random depending on the parent tumour population , 1982, Nature.

[17]  V. Schirrmacher,et al.  High‐frequency generation of new immunoresistant tumor variants during metastasis of a cloned murine tumor line (ESb) , 1982, International journal of cancer.

[18]  P. Nowell The clonal evolution of tumor cell populations. , 1976, Science.

[19]  L. Liotta,et al.  The significance of hematogenous tumor cell clumps in the metastatic process. , 1976, Cancer research.

[20]  F. Miller Tumor subpopulation interactions in metastasis. , 1983, Invasion & metastasis.

[21]  G. Heppner Tumor heterogeneity. , 1984, Cancer research.

[22]  M. Kripke,et al.  Speculations on the role of ultraviolet radiation in the development of malignant melanoma. , 1979, Journal of the National Cancer Institute.

[23]  V. Ling,et al.  Metastatic variants are generated spontaneously at a high rate in mouse KHT tumor. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D. Dexter,et al.  Tumor heterogeneity and drug resistance. , 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[25]  I. Fidler,et al.  Biological diversity in metastatic neoplasms: origins and implications. , 1982, Science.

[26]  I. Fidler,et al.  Metastatic behavior of a murine reticulum cell sarcoma exhibiting organ-specific growth. , 1981, Cancer research.