Immunoselection of tumor variants resistant to antibody-mediated cytotoxicity. Their immunologic and metastatic characterization
- PMID: 6965227
- PMCID: PMC11039299
- DOI: 10.1007/BF00200180
Immunoselection of tumor variants resistant to antibody-mediated cytotoxicity. Their immunologic and metastatic characterization
Abstract
The immunological characteristics of two series of metastatic variants of restricted genetic origin were related to their lung-colony-forming potential. A series of metastatic variants was isolated from a tumor-cell population in which heterogeneity appeared following short-term in vivo passage, while a second series of variants were immunoselected in vitro for resistance to antibody-complement-mediated cell lysis. In the case of the first series, the sensitivity of the individual variants to cell-mediated and antibody-complement-mediated cytotoxicity appeared to be partly determined by the number and rate of loss of antibody-binding sites on the cell surface. These characteristics also correlated with the efficiency of experimental metastasis in the animal. We compared the results reported herein with our previous studies of nonimmune parameters for this series of metastatic variants, and we conclude that immunological differences can be important to the efficiency of lung-colony formation. However, in the case of the second series of variants, despite selection in vitro for resistance to antibody-complement-mediated cell lysis, the behavior of these variants in the lung colony assay could not be predicted by the immunologic parameters examined.
Similar articles
-
Tumor progression in vitro: the paradoxical natural antibody and complement-selected phenotype.Nat Immun Cell Growth Regul. 1987;6(4):189-204. Nat Immun Cell Growth Regul. 1987. PMID: 3683415
-
Alterations in sensitivity to nonspecific cell-mediated lysis associated with tumor progression: characterization of activated macrophage- and natural killer cell-resistant tumor variants.J Natl Cancer Inst. 1984 Aug;73(2):483-91. doi: 10.1093/jnci/73.2.483. J Natl Cancer Inst. 1984. PMID: 6589440
-
Enhanced invasiveness and metastatic potential of epithelial cell lines cultured in the presence of dimethyl sulphoxide.Int J Cancer. 1990 Aug 15;46(2):251-7. doi: 10.1002/ijc.2910460218. Int J Cancer. 1990. PMID: 2384274
-
Tumor progression in metastasis: an experimental approach using lectin resistant tumor variants.Cancer Metastasis Rev. 1982;1(2):99-140. doi: 10.1007/BF00048223. Cancer Metastasis Rev. 1982. PMID: 6764377 Review.
-
Induction of tumor-immune responses and their interaction with the developing tumor.Contemp Top Mol Immunol. 1977;6:177-207. doi: 10.1007/978-1-4684-2841-4_6. Contemp Top Mol Immunol. 1977. PMID: 161526 Review. No abstract available.
Cited by
-
Changes in adhesive properties of tumor cells do not necessarily influence metastasizing capacity.Clin Exp Metastasis. 1989 Mar-Apr;7(2):227-42. doi: 10.1007/BF01787026. Clin Exp Metastasis. 1989. PMID: 2920476
-
Immunologic enhancement of experimental metastasis in the rat.Cancer Immunol Immunother. 1984;17(1):42-50. doi: 10.1007/BF00205496. Cancer Immunol Immunother. 1984. PMID: 6563943 Free PMC article.
References
-
- Bansal SC, Bansal BR, Boland JP. Blocking and unblocking serum factors in neoplasia. Curr Top Microbiol Immunol. 1976;75:45. - PubMed
-
- Brattain MG, Fine WD, Khaled FM, Thomson J, Brattain DE. Heterogeneity of malignant cells from a human colonic carcinoma. Cancer Res. 1981;41:1751. - PubMed
-
- Brown JP, Klitzman JM, Hellstrom KE. A microassay for antibody binding to tumor cell surface antigens using 125I-labelled protein A from Staphylococcus aureus. J Immunol Meth. 1977;15:57. - PubMed
-
- Buxbaum JN, Basch RS. Immunologic basis of resistance to RL ♂ 1 induced by immunoselected Thy-1.2 negative variants. J Immunol. 1980;125:673. - PubMed
-
- Byers VS, Johnston JO. Antigenic differences among osteogenic sarcoma tumor cells taken from different locations in human tumors. Cancer Res. 1977;37:3173. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources