Abstract
Gene therapy is defined as the alteration of the genetic material of a cell with resultant benefit to a patient. Gene transfer has two broad categories: one in which a therapeutic gene is delivered to the cells with the aim of treating a disease; and another where a marker gene is delivered to label a cell type to determine the fate of a cell or the marker gene. Gene therapy is now becoming a rapidly developing therapeutic modality for experimental treatment of some cancers and diseases that have no alternative treatment (1,2).
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
Anderson, W. F. (1992) Human gene therapy. Science 256, 808–813.
Friedman, T. and Roblin, R. (1972) Gene therapy for human genetic diseases. Science 175, 949–955.
Blaese, R. M. (1992) Gene therapy using suicide genes, in Biologic Therapy of Cancer (DeVita Jr., V. T., Hellman, S., and Rosenberg, S. A., eds.), J. B. Lippincot, Philadelphia, PA, pp. 746–750.
Freeman, S. M., McCune, C. S., Abboud, C. N., and Abraham G. N. (1992) Treatment of ovarian cancer using HSV-tK gene-modified cells. Hum. Gene Ther. 3, 342–349.
Moolten, F. L. (1986) Tumor chemosensitivity conferred by inserted herpes thymidine kinase genes: paradigm for a prospective cancer control strategy. Cancer Res. 46, 5276–5281.
Elion, G. B. (1980) The chemotherapeutic exploitation of virus specified enzymes. Adv. Enzyme Regul. 18, 53–60.
Elion, G. B., Furman, P. A., Fyfe, J. A., deMiranda, P., Beauchamp, L., and Schaeffer, H. J. (1977) Selectivity of action of an antiherpetic agent, 9-(2-hydroxyethoxymethyl) guanine. Proc. Natl. Acad. Sci. USA 74, 5716–5720.
Shepp, D. H., Dandliker, P., deMiranda, P., Burnette, T. C., Cederberg, D. M., Kirk, L. E., and Meyer, J. D. (1985). Activity of 9-[2-hydroxymethyl) ethoxymethyl guanine in the treatment of cytomegalovirus penumonia. Ann. Intern. Med. 103, 368–373.
Moolten, F. L. (1990a) Mosaicism induced by gene insertion as a means of improving chemotherapeutic selectivity. Crit. Rev. Immunol. 10, 203–233.
Moolten, F. and Wells, J. M. (1990b) Curability of tumors bearing herpes thymidine kinase genes transferred by retroviral vectors. J.Natl. Cancer Inst. 82, 297–300.
Freeman, S. M., Whartenby, K. A., Koeplin, D. S., Moolten, F. L., Abboud, C. N., and Abraham, G. N. (1992b) Tumor regression when a fraction of the tumor mass contains the HSV-tK gene. J. Cell Biochem. 16F (abstr. 47).
Freeman, S. M., Abboud, C. N., Whartenby, K. A., Packman, C. H., Koeplin, D. S., Moolten, F. L., and Abraham, G. N. (1993) The Bystander effect: tumor regression when a fraction of the tumor mass is genetically modified. Cancer Res. 53, 5274–5283.
Bi, W. L., Parysek, L. M., Warnick, R., and Stambrook, P. J. (1993) In vitro evidence that metabolic cooperation is responsible for the Bystander Effect observed with HSV-tK retroviral gene therapy. Hum. Gene Ther. 4, 725–731.
Mesnil, M., Piccoli, C., Tiraby, G., Willecke, K., and Yamasaki, H. (1996) Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins. Proc. Natl. Acad. Sci. USA 93, 1831–1835.
Freeman, S. M., Ramesh, R., Shastri, M., Munshi, A., Jensen, A., and Marrogi, A. J. (1995) The role of cytokines in mediating the bystander effect usingHSV-tK xenogeneic cells.Cancer Lett. 92, 167–174.
Barba, D., Hardin, J., Ray, J., and Gage, F. H. (1993) Thymidine kinase mediated killing of rat brain tumors. J. Neurosurg. 79, 729–735.
Culver, K. W., Ram, Z., Oldfield, E. H., and Blaese, M. (1992) Regression of brain tumors using gene-modified cells. Science 256, 1550–1552.
Ram, Z., Culver, K. W., Walbridge, S. W., Blaese, R. M., and Oldfield, E. H. (1993) In situ retroviral-mediated gene transfer for the treatment of brain tumors. Cancer Res. 53, 83–88.
Ezzedine, Z. D., Martuza, R. L., Platika, D., Short, M. P., Malick, T., Choi, B., et al. (1991) Selective killing of glioma cells in culture and in vivo by retrovirus transfer of the Herpes Simplex thymidine kinase gene. New Biol. 3, 608–614.
Freeman, S. M., McCune, C., Robinson, W., Abboud, C. N., Angel, C., Abraham G. N., et al. (1995) Treatment of ovarian cancer using a gene-modified vaccine. Hum. Gene Ther. 6, 927–939.
Freeman, S. M., Ramesh, R., Munshi, A., Abboud, C. N., and Marrogi, A. J. (1995) Enhanced tumor recognition and killing using the HSV-tK suicide gene. Cancer Gene Ther. 2, 240–241.
Ramesh, R., Marrogi, A. J., Munshi, A., Abboud, C. N., and Freeman, S. M. (1996) In-vivo analysis of the “Bystander effect”: a cytokine cascade. Exp. Hematol. 24, 829–838.
Gagandeep, S., Brew, R., Green, B., Christmas, S. E., Klatzman, D., Poston, G. J., and Kinsella, A. R. (1996) Prodrug activated gene therapy. Involvement of an immunological component in the bystander effect. Cancer Gene Ther. 3, 83–88.
Boring, C. C., Squires, T. S., and Tong, T. (1993) Cancer statistics, 1993. CA Cancer J. Clin. 43, 7–26.
Cornetta, K. and Anderson, W. F. (xxxx) Protamine sulfate as an effective alternative to polybrene in retroviral-mediated gene-transfer: implications for human gene therapy. J.Virol. 23, 187–194.
Aaronson, S. A., Bassin, R. H., and Weaver, C. (1972) Comparison of the murine sarcoma viruses in non-producer and S+/L−transformed cells. J.Virol. 9, 701–704.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2000 Humana Press Inc., Totowa, NJ
About this protocol
Cite this protocol
Ramesh, R., Munshi, A., J. Marrogi, A., M. Freeman, S. (2000). Retroviral Transfer of the Herpes Simplex Virus-Thymidine Kinase (HSV-tK) Gene for the Treatment of Cancer. In: Walther, W., Stein, U. (eds) Gene Therapy of Cancer. Methods in Molecular Medicine™, vol 35. Humana Press. https://doi.org/10.1385/1-59259-086-1:479
Download citation
DOI: https://doi.org/10.1385/1-59259-086-1:479
Publisher Name: Humana Press
Print ISBN: 978-0-89603-714-4
Online ISBN: 978-1-59259-086-5
eBook Packages: Springer Protocols