Identification of melanoma cell surface antigens immunogenic in mice.

Active immunization to B16 melanoma cells or vaccines induces anti-melanoma immune responses in syngeneic mice. The immunogenic antigens stimulating immunity to this tumor have not been identified. In this study we detected several B16 melanoma antigens immunogenic in syngeneic mice using as probes antimelanoma antibodies induced by immunization to B16 melanoma vaccines. These antigens were identified by SDS-PAGE and autoradiographic analysis of specific immunoprecipitates. They were cell-surface components with approximate molecular weights of 41, 46, 50, 75, 80, and 104 KD. All these antigens were expressed by syngeneic and xenogeneic melanomas and by some unrelated syngeneic tumors but not by normal syngeneic cells, xenogeneic melanocytes, or by B16 melanoma cells obtained from fresh tumors or grown in defined medium. The antigens were distinct from murine viral antigens expressed by B16 melanoma cells and from components of the culture medium used to grow cells for vaccine production. These results indicate that several B16 melanoma cell-surface antigens are immunogenic in syngeneic mice. Expression of these antigens appears to be related to malignant transformation as they were found on all melanomas studied, and some other cancers, but not on normal cells.

[1]  S. Orlow,et al.  Induction of B16 melanoma melanogenesis by a serum-free synthetic medium. , 1992, Experimental cell research.

[2]  J. Bystryn,et al.  Effect of cell wall skeleton and monophosphoryl lipid A adjuvant on the immunogenicity of a murine B16 melanoma vaccine. , 1991, Journal of the National Cancer Institute.

[3]  G. Nicolson,et al.  Differential expression of a Mr approximately 90,000 cell surface transferrin receptor-related glycoprotein on murine B16 metastatic melanoma sublines selected for enhanced brain or ovary colonization. , 1990, Cancer research.

[4]  A. Kimura,et al.  Poorly metastatic tumor cell variants as primary targets of syngeneic antibody responses against murine melanoma. , 1989, Cancer research.

[5]  M. Pittelkow,et al.  Growth of Normal Human Melanocytes in a Defined Medium , 1988 .

[6]  M. Taniguchi,et al.  Characterization of a melanoma antigen with a mouse-specific epitope recognized by a monoclonal antibody with antimetastatic ability. , 1988, Cancer research.

[7]  Z. L. Herd Suppression of B16 melanoma lung colonization by syngeneic monoclonal antibodies. , 1987, Cancer research.

[8]  J. Price,et al.  Phenotypic diversity of murine B16 melanoma detected by anti-B16 monoclonal antibodies. , 1987, Cancer research.

[9]  V. Hearing,et al.  Monoclonal antibody production to a B16 melanoma associated antigen , 1985, International journal of cancer.

[10]  J. Bystryn,et al.  Effect of tunicamycin on release of macromolecules and tumor antigens by human melanoma cells. , 1985, Cancer research.

[11]  R. E. Cunningham,et al.  Expression of a murine B16 melanoma-associated antigen analyzed by flow cytometry. , 1985, The Journal of surgical research.

[12]  M. Taniguchi,et al.  Syngeneic monoclonal antibodies against melanoma antigens with species specificity and interspecies cross-reactivity. , 1984, The Journal of investigative dermatology.

[13]  N. Smorodinsky,et al.  B16 melanoma development, NK activity cytostasis and natural antibodies in 3 and 12 month old mice. , 1984, British Journal of Cancer.

[14]  T. Irimura,et al.  Carbohydrate chain analysis by lectin binding to electrophoretically separated glycoproteins from murine B16 melanoma sublines of various metastatic properties. , 1984, Cancer research.

[15]  W. Birchmeier,et al.  Monoclonal antibodies that prevent adhesion of B 16 melanoma cells and reduce metastases in mice: crossreaction with human tumor cells. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. Cairncross,et al.  Surface antigens of melanocytes and melanomas. Markers of melanocyte differentiation and melanoma subsets , 1982, The Journal of experimental medicine.

[17]  M A Markwell,et al.  A new solid-state reagent to iodinate proteins. I. Conditions for the efficient labeling of antiserum. , 1982, Analytical biochemistry.

[18]  J. Marchalonis,et al.  Demonstration and isolation of murine melanoma-associated antigenic surface proteins. , 1979, Biochemical and biophysical research communications.

[19]  A. Kopf,et al.  Growth and immunogenicity of murine B-16 melanoma. , 1974, The Journal of investigative dermatology.

[20]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.