Abstract
Gene therapy represents a strategy using transfer of genetic information to modify a population of target cells for therapeutic purposes. The transferred genetic material has typically included double-stranded deoxyribonucleic acid (DNA), but occasionally single-stranded DNA and even ribonucleic acid (RNA). Gene therapy represents one of the many novel “targeted” antineoplastic treatment approaches with the goal to inhibit the growth of tumor cells and spare normal cells. The use of gene therapy relevant to cancer treatment includes the in vivo genetic modification of tumors or the tumor-bearing host, as well as the ex vivo genetic manipulation of cell populations, which are then administered to the tumor-bearing host.
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Korst, R.J., Crystal, R.G. (2005). Cancer-Related Gene Therapy Clinical Trials. In: Curiel, D.T., Douglas, J.T. (eds) Cancer Gene Therapy. Contemporary Cancer Research. Humana Press. https://doi.org/10.1007/978-1-59259-785-7_28
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