A Novel Method of Boron Delivery Using Sodium Iodide Symporter for Boron Neutron Capture Therapy
Author(s) -
Sanath Kumar,
Svend O. Freytag,
Kenneth Barton,
Jay Burmeister,
Michael C. Joiner,
Bijan Sedghi,
Benjamin Movsas,
Peter J. Binns,
Jae Ho Kim,
Stephen L. Brown
Publication year - 2010
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.10036
Subject(s) - sodium iodide symporter , boron , transfection , glioma , symporter , sodium iodide , chemistry , cancer research , neutron capture , iodine , radiochemistry , microbiology and biotechnology , medicine , biology , biochemistry , organic chemistry , transporter , gene
Boron Neutron Capture Therapy (BNCT) effectiveness depends on the preferential sequestration of boron in cancer cells relative to normal tissue cells. We present a novel strategy for sequestering boron using an adenovirus expressing the sodium iodide symporter (NIS). Human glioma grown subcutaneously in athymic mice and orthotopic rat brain tumors were transfected with NIS using a direct tumor injection of adenovirus. Boron bound as sodium tetrafluoroborate (NaBF(4)) was administered systemically several days after transfection. Tumors were excised hours later and assessed for boron concentration using inductively coupled plasma atomic emission spectroscopy. In the human glioma transfected with NIS, boron concentration was more than 10 fold higher with 100 mg/kg of NaBF(4), compared to tumor not transfected. In the orthotopic tumor model, the presence of NIS conferred almost 4 times the boron concentration in rat tumors transfected with human virus compared with contralateral normal brain not transfected. We conclude that adenovirus expressing NIS has the potential to be used as a novel boron delivery agent and should be explored for future clinical applications.
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