Metastasis-related cell functions in primary and metastatic tumor cells of AKR lymphoma

• Published in: Cancer letters 1996-03, Vol.101 (2), p.219-225
• Main Authors: Klein, O., Savion, N., Staroselsky, A., Donin, N., Huszar, M., Wollman, Y., Leibovici, J.
• Format: Article
• Language: English
• Subjects: AKR lymphoma; Animal tumors. Experimental tumors; Animals; Biological and medical sciences; Cell Adhesion; Cell Division; Cell Movement; Endothelium; Experimental malignant blood diseases; Extracellular Matrix; Female; Kidney Neoplasms - secondary; Lymphoma - pathology; Lymphoma - physiopathology; Medical sciences; Metastatic phenotype; Mice; Mice, Inbred AKR; Neoplasm Metastasis - physiopathology; Phenotype; Splenic Neoplasms - secondary; Tumor Cells, Cultured; Tumor progression model; Tumors
• ISSN: 0304-3835; 1872-7980
• DOI: 10.1016/0304-3835(96)04138-9

The metastatic phenotype is of extreme complexity. To complete all the stages of metastasis, the tumor cell must possess a whole series of functional abilities. Multiple biological markers are therefore needed to achieve a deeper understanding of the metastatic phenotype. In the present study we compared primary (PT) to metastatic tumor (MT) cells of two AKR lymphoma variants with respect to several cellular functions relevant to various steps of tumor dissemination. The MT cells of the TAU-44 variant had a higher capacity than the PT cells to attach to endothelial monolayers and ECM, exhibited a more elevated motility and a higher capacity to grow in the spleen as a metastatic target organ. However, the TAU-44-MT cells had a lower ability to grow in the kidney than the PT cells. The TAU-33-MT cells had a higher ability to attach to endothelial cells and to grow in both spleen and kidney but were less motile compared to PT cells. Metastatic cells showed, on the whole, higher ability to perform in most, but not all, stage-specific models than primary tumor cells.