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The systemic delivery of an oncolytic adenovirus expressing decorin inhibits bone metastasis in a mouse model of human prostate cancer.

Abstract
In an effort to develop a new therapy for prostate cancer (PCa) bone metastases, we have created Ad.dcn, a recombinant oncolytic adenovirus carrying the human decorin gene. Infection of PC-3 and DU-145, the human prostate tumor cells, with Ad.dcn or a non-replicating adenovirus Ad(E1-).dcn resulted in decorin expression; Ad.dcn produced high viral titers and cytotoxicity in human prostate tumor cells. Adenoviral-mediated decorin expression inhibited Met, the Wnt/β-catenin signaling axis, vascular endothelial growth factor A, reduced mitochondrial DNA levels and inhibited tumor cell migration. To examine the antitumor response of Ad.dcn, PC-3-luc cells were inoculated in the left heart ventricle to establish bone metastases in nude mice. Ad.dcn, in conjunction with control replicating and non-replicating vectors were injected via tail vein. The real-time monitoring of mice, once a week, by bioluminescence imaging and X-ray radiography showed that Ad.dcn produced significant inhibition of skeletal metastases. Analyses of the mice at the terminal time point indicated a significant reduction in the tumor burden, osteoclast number, serum tartrate-resistant acid phosphatase 5b levels, osteocalcin levels, hypercalcemia, inhibition of cancer cachexia and an increase in the animal survival. Based on these studies, we believe that Ad.dcn can be developed as a potential new therapy for PCa bone metastasis.
AuthorsW Xu, T Neill, Y Yang, Z Hu, E Cleveland, Y Wu, R Hutten, X Xiao, S R Stock, D Shevrin, K Kaul, C Brendler, R V Iozzo, P Seth
JournalGene therapy (Gene Ther) Vol. 22 Issue 3 Pg. 247-56 (Mar 2015) ISSN: 1476-5462 [Electronic] England
PMID25503693 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Decorin
Topics
  • Animals
  • Bone Neoplasms (secondary, therapy)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Decorin (genetics, metabolism, pharmacology)
  • Disease Models, Animal
  • Gene Transfer Techniques
  • Humans
  • Male
  • Mice, Nude
  • Oncolytic Virotherapy
  • Oncolytic Viruses (genetics, metabolism)
  • Prostatic Neoplasms (therapy)

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