Enhanced antiproliferative activity by metastatic RAW117 lymphoma cells View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1991-01

AUTHORS

S. S. Joshi, S. J. O'connor, D. D. Weisenburger, J. G. Sharp, H. M. Gharpure, K. W. Brunson

ABSTRACT

The highly malignant/metastatic murine large cell lymphoma cell line RAW117-H10 forms 100-200 times more liver metastatic tumors than its parental counterpart cell line RAW117-P. RAW117-H10 cells, but not the less malignant/metastatic parental cells, significantly inhibited the mitogen-induced proliferation of normal syngeneic Balb/c and allogeneic ICRC mouse spleen cells. Such an inhibition also occurred when mitomycin-C treated metastatic lymphoma cells were added 24 h after initiation of culture, indicating that no competition with mitogen binding sites on the lymphocytes was necessary for inhibition of proliferation. 'Antiproliferative' cell surface molecules were extracted non-cytolytically from the RAW117-H10 cells using butanol. The butanol extracts from the metastatic RAW117-H10 cells also inhibited the mitogen-induced proliferation and natural killer (NK) cell-mediated cytotoxicity of normal spleen cells. Our results indicate that these 'antiproliferative' cell surface molecules of metastatic murine RAW117-H10 lymphoma cells may have important role(s) in tumor-mediated host immunosuppression. More... »

PAGES

27-37

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01831707

DOI

http://dx.doi.org/10.1007/bf01831707

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014273060

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2015714


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