Focal Therapy for Prostate Cancer: A Molecular Biology Approach with TRAIL View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2017

AUTHORS

Vikram Narayan , Badrinath R. Konety , Thomas S. Griffith

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. More... »

PAGES

347-354

Book

TITLE

Imaging and Focal Therapy of Early Prostate Cancer

ISBN

978-3-319-49910-9
978-3-319-49911-6

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-319-49911-6_26

DOI

http://dx.doi.org/10.1007/978-3-319-49911-6_26

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53 schema:description 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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