INCREASED METASTATIC CAPACITY OF LEWIS LUNG-TUMOR CELLS BY INVIVO SELECTION PROCEDURE
- 1 January 1983
- journal article
- research article
- Vol. 3 (3) , 174-182
Abstract
Lewis [mouse] lung tumors cells from liver metastases originally obtained from an intrasplenic tumor, and lung metastases obtained from an i.m. transplant, were repeatedly passaged in the corresponding transplantion sites (spleen, intramuscular). Cells from liver metastases injected into the spleen gained an increased metastatic capacity. The same phenomenon was observed with lung metastatic cells injected i.m., but to a lesser degree. In all passages metastases occurred only in the organs receiving the veous blood from the primary site. The enhanced metastasis formation may be a result of a selection of tumor cells resistant to host cytotoxic cells and/or of selection of tumor cells seeding successfully in target organs.This publication has 9 references indexed in Scilit:
- Experimental model for liver metastasis formation using lewis lung tumorZeitschrift für Krebsforschung und Klinische Onkologie, 1982
- High-frequency generation of new immunoresistant tumor variants during metastasis of a cloned murine tumor line (ESb)International Journal of Cancer, 1982
- Distinct lung-colonizing and lung-metastasizing cell populations in B16 mouse melanomaNature, 1981
- METASTATIC BEHAVIOR OF A MURINE RETICULUM-CELL SARCOMA EXHIBITING ORGAN-SPECIFIC GROWTH1981
- Murine melanoma: a model for intracranial metastasisBritish Journal of Cancer, 1980
- Effect of combined surgical and chemotherapeutic treatment on Lewis lung carcinomaZeitschrift für Krebsforschung und Klinische Onkologie, 1980
- Liver‐colonizing melanoma cells selected from B‐16 melanomaInternational Journal of Cancer, 1979
- Mechanisms of metastasisBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1979
- Selection of malignant melanoma variant cell lines for ovary colonizationJournal of Supramolecular Structure, 1979