期刊
NUCLEAR MEDICINE AND BIOLOGY
卷 33, 期 4, 页码 575-580出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2006.01.011
关键词
sodium iodide symporter (NIS); Tc-99m-pertechnetate; uptake; hepatoma; tissue-specific expression
The sodium iodide symporter (NIS) gene could be used as an ideal reporter gene as well as a promising therapeutic gene. Tc-99m-pertechnetate has proven to be more advantageous than I-131-iodide with respect to image quality, procedure and radiation dose ill examination of thyroid uptake and scintigraphy. Herein, we investigated the feasibility of monitoring human sodium iodide symporter (hNIS) gene expression with Tc-99m-pertechnetate in hepatoma cells (MH3924A) following tissue-specific expression. Methods: MH3924A cells were stably transfected with the recombinant retroviral vector, in which hNIS cDNA was driven by murine albumin enhancer/promoter (mAlb) and coupled to hygromycin resistance gene using an internal ribosomal entry site. Functional NIS expression in hepatoma cells was confirmed by an I-125(-) uptake assay. The dynamic uptake and efflux of Tc-99m-pertechnetate was determined both in vitro and in vivo. Results: The Tc-99m-pertechnetate was up to 254-fold higher in stably transfected MH3924A cells than in wild-type cells. However, the in vitro efflux of Tc-99m-pertechnetate out of recombinant cells was rapid with a half-life of less than 2 min. Further, the in vivo Studies yielded clear images and quantitative data of mAlbhNIS-infected tumor xenografts using Tc-99m-pertechnetate and gamma camera. Conclusion: The current study demonstrates enhanced Tc-99m-pertechnetate uptake in hepatoma cells in vitro and in vivo following tissue-specific gene transfer using a recombinant retrovirus with the albumin enhancer/promoter and the hNIS gene. It is feasible to monitor hNIS gene expression noninvasively and quantitatively using conventional gamma camera and Tc-99m-pertechnetate. (c) 2006 Elsevier Inc. All rights reserved.
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