Abstract
The treatment of metastatic cancer remains the preeminent problem in neoplasia. Despite significant advances in our understanding of some of the molecular mechanisms in carcinogenesis and tumor progression, our ability to translate these findings into clinical treatment remains limited. While these molecular studies evolve, the more immediate need for new treatment modalities has led to a more intense evaluation of current approaches to therapy, including surgery, radiation and chemotherapy. In addition, we have also seen a resurgent interest in immunotherapy, which has led to promising approaches in some diseases. Unfortunately, the goal of developing specific systemic immunotherapy remains elusive. In this manuscript we will describe some ideas we have used in our attempt to treat established metastases in murine models.
Supported in part by PHS Grants 38853 and 41525 and The Sid Richardson Foundation
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References
Boon T, Kellerman O (1977) Rejection by syngeneic mice of cell variants obtained by mutagenesis of a malignant teratocarcinoma cell line. Proc Nati Acad Sci 74: 272–275
Boon T (1983) Antigenic tumor cell variants obtained with mutagens. Adv Cancer Res 39: 121–151
Carlow DA, Kerbel RS, Elliott BE (1989) Failure of expression of class I major histocompatibility antigens to alter tumor immunogenicity of a spontaneous murine carcinoma. J Nati Cancer Inst 81: 759–767
Dexter DL, Calabresi P (1982) Intraneoplastic diversity. Biochem Biophys Acta 695: 97–112
Esumi N, Hunt B, Itaya T, Frost P (1991) The reduced tumorigenicity of murine tumor cells secreting interferon gamma is due to non-specific host responses and is unrelated to class I MHC expression. Cancer Res 51: 1185–1189
Fearon ER, Itaya T, Hunt B, Vogelstein B, Frost P (1988) Induction in a murine tumor of immunogenic tumor variants by transfection with a foreign gene. Cancer Res 48: 2975–2980
Fearon ER, Pardoll DM, Itaya T, et al. (1990) Interleukin-2 production by tumor cells bypasses T helper function in the generation of an antitumor response. Cell 60: 397–403
Frost P, Kerbel R, Bauer E, Tartamella-Biondo R, Cefalu W (1978) Mutagen treatment as a means for selecting immunogenic variants from otherwise poorly immunogenic malignant tumors. Cancer Res 43: 125–132
Frost P, Liteplo RG, Donaghue TP, Kerbel RS (1984) Selection of strongly immunogenic “Tum” variants from tumors at high frequency using 5-azacytidine. J Exp Med 159: 1491–1501
Heppner GH (1984) Tumor heterogeneity. Cancer Res 44: 2259–2265
Itaya T, Hunt B, Frost P (1989) Retention of immunogenicity after X-irradiation of mouse colon tumor cells expression the transfected influenze virus hemagglutinin gene. Cancer Immunol Immunother 28: 248–252
Janis E, Kaufmann SE, Schwartz RH, Pardoll DM (1989) Activation of gamma/delta T cells in the primary immune response to Mycobacterium tuberculosis. Science 244: 713–716
Kerve JA, Foreman J (1982) Helper activity is required for the in vivo generation of cytotoxic T lymphocytes. J Exp Med 155: 768–782
Lake P, Mitchinson NA (1976) Associative control of the immune response to cell surface antigens. Immunol Commun 5: 795–805
Mory Y, Chernajovsky Y, Feinstein SI, et al. (1981) Synthesis of human interferon ß1 in Escherichia coli infected by a lambda phage recombinant containing a human genomic fragment. Eur J Biochem 120: 197–202
Sibille C, Chomez P, Wildmann C, et al. (1990) Structure of the gene of tum transplantation antigen P198: a point mutation generates a new antigenic peptide. J Exp Med 172: 35–45
Tanaka E, Isselbacher KS, Khoury G, Jay G (1985) Reversal of oncogenesis by the expression of a major histocompatibility complex class I gene. Science 228: 26–30
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© 1992 Springer-Verlag Berlin Heidelberg
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Frost, P. (1992). Alien Gene Transfection and the Immune Response to Tumors. In: Staehler, G., Pomer, S. (eds) Basic and Clinical Research on Renal Cell Carcinoma. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76863-7_13
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DOI: https://doi.org/10.1007/978-3-642-76863-7_13
Publisher Name: Springer, Berlin, Heidelberg
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