A preclinical large animal model of adenovirus-mediated expression of the sodium-iodide symporter for radioiodide Imaging and therapy of locally recurrent prostate cancer

被引:47
作者
Dwyer, RM
Schatz, SM
Bergert, ER
Myers, RM
Harvey, ME
Classic, KL
Blanco, MC
Frisk, CS
Marler, RJ
Davis, BJ
O'Connor, MK
Russell, SJ
Morris, JC
机构
[1] Mayo Clin Rochester, Dept Endocrinol & Internal Med, Rochester, MN 55905 USA
[2] Mayo Clin Rochester, Dept Endocrinol, Rochester, MN 55905 USA
[3] Mayo Clin Rochester, Dept Urol, Rochester, MN 55905 USA
[4] Mayo Clin Rochester, Program Mol Med, Rochester, MN 55905 USA
[5] Mayo Clin Rochester, Dept Comparat Med, Rochester, MN 55905 USA
[6] Mayo Clin Rochester, Div Radiat Oncol, Rochester, MN 55905 USA
[7] Mayo Clin Rochester, Dept Radiol, Rochester, MN 55905 USA
[8] Mayo Clin Scottsdale, Dept Mol Pharmacol & Expt Therapeut, Scottsdale, AZ 85259 USA
关键词
sodium iodide symporter; gene therapy; adenovirus; radioiodine; prostate cancer;
D O I
10.1016/j.ymthe.2005.05.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The sodium-iodide symporter (NIS) is primarily a thyroid protein, providing for the accumulation of iodide for biosynthesis of thyroid hormones. Native NIS expression has made possible the use of radioactive iodide to image and treat thyroid disease successfully. The current study, using adult male beagle dogs, was carried out in preparation for a Phase I clinical trial of adenovirus-mediated NIS gene (approved symbol SLC5A5) therapy for prostate cancer. Direct intraprostatic injection of virus (Ad5/CMV/NS) was followed by iv injection of 3 mCi I-123 and serial image acquisition. The dogs were then given a therapeutic dose of I-131 (116 mCi/m(2)) and observed for 7 days. SPECT/CT fusion imaging revealed clear images of the NIS-transcluced prostates. Dosimetry calculations revealed an average absorbed dose to the prostate of 23 +/- 42 cGy/mCi I-131, with acceptably low radiation doses to other organs. This study demonstrated the successful introduction of localized NIS expression in the prostate gland of dogs, with no vector-related toxicity observed. None of the animals experienced any surgical complications, and serum chemistry panels showed no significant change following therapy. The results presented provide further evidence of the safety and efficacy of NIS as a therapeutic gene and support translation of this work into the clinical setting.
引用
收藏
页码:835 / 841
页数:7
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