Hyperthermia and gene therapy: Potential use of MicroPET imaging Journal Article


Authors: Li, G. C.; He, F.; Ling, C. C.
Article Title: Hyperthermia and gene therapy: Potential use of MicroPET imaging
Abstract: In recent years, both hyperthermia and gene-therapy have been evaluated as approaches to improve cancer radiotherapy. In addition, potential exists to combine these approaches to increase the overall therapeutic efficacy. For example, it has been reported that adenovirus-mediated heat-inducible gene expression may reduce the normal tissue toxicity associated with constitutively controlled expression of therapeutic genes. In our laboratory, we have shown that adenovirus-mediated, heat-activated antisense Ku70 expression radiosensitizes tumor cells in vitro and in vivo, suggesting a novel approach to use heat-activated gene-radiotherapy to radiosensitize human tumors. However, to optimize the application of heat-activated gene-radiotherapy in the clinic, we need to develop techniques to improve the delivery of the therapeutic adenovirus and to verify/monitor the delivery non-invasively. In an ongoing study we test the effect of mild hyperthermia in improving adenovirus-medicated vector delivery in a mouse tumor model. In addition, we evaluate the use of non-invasive microPET imaging to monitor the spread of the adenoviral vector. Our preliminary results show that (1) microPET imaging can be used to monitor non-invasively the viral vector delivery and dissemination, and (2) mild heat shock leads to significantly improved viral vector distribution, in other words, a wider spatial spread, in vivo. Here, we will present a short review on the current status of hyperthermia and heat-activated gene-radiotherapy, and the potential use of PET imaging in gene therapy. © 2006 Taylor & Francis.
Keywords: nonhuman; conference paper; cancer radiotherapy; combined modality therapy; positron emission tomography; neoplasms; monitoring; animals; mice; dna repair; melanoma; gene expression; green fluorescent protein; in vivo study; in vitro study; diagnostic imaging; viral gene delivery system; genetic vectors; double stranded dna; positron-emission tomography; tumor cell; gene therapy; pet imaging; thymidine kinase; heat shock protein 70; adenovirus vector; hyperthermic therapy; hyperthermia; hyperthermia, induced; ku antigen; fluorine 18; non invasive procedure; interleukin 12; radiosensitization; heat shock; adenoviridae; 5 ethyl 2' fluorouracil arabinoside; dna dependent protein kinase
Journal Title: International Journal of Hyperthermia
Volume: 22
Issue: 3
ISSN: 0265-6736
Publisher: Taylor & Francis Group  
Date Published: 2006-05-01
Start Page: 215
End Page: 221
Language: English
DOI: 10.1080/02656730600784677
PUBMED: 16754341
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 10" - "Export Date: 4 June 2012" - "CODEN: IJHYE" - "Source: Scopus"
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  1. Gloria C Li
    132 Li
  2. Fuqiu He
    24 He
  3. C Clifton Ling
    331 Ling