Gene therapy for cancer /

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Bibliographic Details
Imprint:Totowa, N.J. : Humana Press, c2007.
Description:1 online resource (xi, 469 p.) : ill. (some col.)
Language:English
Series:Cancer drug discovery and development
Cancer drug discovery and development.
Subject:Cancer -- Gene therapy.
Neoplasms -- genetics.
Neoplasms -- therapy.
Gene Therapy -- methods.
Cancer -- Gene therapy.
Electronic books.
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/8884173
Hidden Bibliographic Details
Other authors / contributors:Hunt, Kelly K.
Vorburger, Stephan A.
Swisher, Stephen G.
ISBN:9781597452229
159745222X
1588294722 (alk. paper)
9781588294722 (alk. paper)
Notes:Includes bibliographical references and index.
Description based on print version record.
Other form:Print version: Gene therapy for cancer. Totowa, N.J. : Humana Press, c2007 1588294722 9781588294722
Description
Summary:The possibility of treating cancer, a disease defined by genetic defects, by introducing genes targeting these very alterations has led to an immense interest in gene therapy for cancer. Although incremental successes have been realized, enthusiasm for gene therapy has declined due to an increasing number of obstacles. These obstacles include vector systems that do not reach systemic metastases, therapeutic genes with redundant mec- nisms allowing for cellular resistance, and toxicities in clinical trials leading to premature closure of these studies. Different tactics to overcome or circumvent these obstacles have catalyzed the development of a wide range of gene therapy approaches. Thus far, almost two-thirds of gene therapy trials have focused on cancer. This reflects the concept that gene therapy approaches for the treatment of cancer do not necessarily require long-term expression of the gene as is necessary for the treatment of primary genetic defects like hemophilia or juvenile diabetes. Unlike the treatment of genetic defects, where expr- sion of the corrected gene needs to be strong, permanent and, sometimes regulated, tactics to treat tumors can be based on temporary and locally limited effects. In addition, cancer cells have different properties than normal cells and this allows for targeting gene therapy to specific cells, a major advantage over current antitumor therapies, which are also toxic to normal cells and tissues.
Physical Description:1 online resource (xi, 469 p.) : ill. (some col.)
Bibliography:Includes bibliographical references and index.
ISBN:9781597452229
159745222X
1588294722 (alk. paper)
9781588294722 (alk. paper)