Abstract
Definitive treatment of prostate cancer is limited to radical surgery or radiation therapy for localized or regional disease. Localized therapy of solid tumors has been successful in a number of settings, and the treatment of prostate cancer with local (intraprostatic) regimens, such as cryotherapy and brachytherapy, is a common practice. Gene transfer technology offers the potential for the development of new therapies for prostate cancer, with several experimental viral-based studies serving as current treatment options. Of the viral-based therapies, published data indicate minimal toxicity for adenovirus (Ad) injection into the prostate up to doses of 1011 plaque-forming units (pfu). Recombinant Ad vectors infect a wide range of proliferating and quiescent cell types, making this gene delivery system a suitable tool for studying diseases, vaccine therapy, and potential clinical use. Moreover, recombinant Ad is structurally stable and can be prepared and purified to high titers, and wild-type Ad infections are extremely common in the general population, giving Ad a well-documented safety record. Our group has been investigating the potential of a recombinant, replication-deficient adenoviral vector encoding the cDNA for the tumor necrosis factor (TNF) superfamily member TNF-related apoptosis-inducing ligand (Ad5-TRAIL) as a therapeutic agent for prostate cancer. Ad5-TRAIL infection results in the rapid transcription and translation of the transferred TRAIL cDNA into functional TRAIL protein that, when expressed on the cell surface, induces apoptotic death in TRAIL-sensitive prostate tumor cell targets but not normal prostate cells. This chapter outlines the use of Ad gene transfer technology as a novel focal therapy for prostate cancer.
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Narayan, V., Konety, B.R., Griffith, T.S. (2017). Focal Therapy for Prostate Cancer: A Molecular Biology Approach with TRAIL. In: Polascik, T. (eds) Imaging and Focal Therapy of Early Prostate Cancer. Current Clinical Urology. Springer, Cham. https://doi.org/10.1007/978-3-319-49911-6_26
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DOI: https://doi.org/10.1007/978-3-319-49911-6_26
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