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Pretargeting in tumored mice with radiolabeled morpholino oligomer showing low kidney uptake

  • Molecular Imaging
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European Journal of Nuclear Medicine and Molecular Imaging Aims and scope Submit manuscript

Abstract

We have recently shown that accumulation in mouse kidneys of technetium-99m labeled phosphorodiamidate morpholinos (MORFs) increases with the number of cytosines in the base sequence. To improve tumor/kidney ratios in tumored mice, pretargeting studies were performed with a cytosine-free MORF. An 18-mer MORF (5′-TCTTCTACTTCACAACTA) was conjugated to the anti-CEA antibody MN14 (Immunomedics) and administered to nude mice bearing LS174T tumors. Thereafter, the 99mTc-labeled cytosine-free cMORF (5′-TAGTTGTGAAGTAGAAGA-amide-MAG3) was administered. For comparison, the identical study was repeated but with our original pair of 18-mer MORFs (5′-GGGTGTACGTCACAACTA-conjugated MN14 and 99mTc-labeled 5′-TAGTTGTGACGTACACCC-amide-MAG3). Surface plasmon resonance was used to show that the hybridization affinities of the original and the modified pair of MORFs were essentially equal. Hybridization of the cytosine-free cMORF-99mTc to MN14-MORF was demonstrated in vitro by size-exclusion high-performance liquid chromatography. At 3 h, kidney levels in normal mice were 2.0%ID/organ for the modified cMORF vs. 4.1%ID/organ for the original cMORF sequence, while at 24 h, these values were 0.9% vs 1.8%ID/organ. Pretargeting studies in tumored mice receiving 25 μg of conjugated antibody, 0.5 μg of labeled cMORF 48 h later, followed by imaging and sacrifice at 3 h showed that kidney levels were reduced using the cytosine-free cMORF. Moreover, tumor accumulation was about 3.6%ID/g and was independent of sequence. The whole-body images clearly reflected the improved tumor to kidney ratios. By choosing a cytosine-free base sequence for pretargeting studies, kidney accumulation of cMORF-99mTc was reduced without adversely influencing tumor accumulation. The lowering of kidney radioactivity levels in this way may be important to reduce toxicity to this organ in connection with pretargeting radiotherapy studies.

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Acknowledgements

The authors are grateful to Dr. Gary L. Griffiths of Immunomedics (Morris Plains, NJ) for providing the MN14 and to Dr. James Summerton (Philomath, OR) for useful discussion concerning MORF modification. We also thank Loretta Lee of the UMMS Tissue Culture Center for maintaining the LS174T tumor cells. Financial support for this investigation was provided in part by the National Institutes of Health (CA79507 and CA94994).

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Correspondence to Donald J Hnatowich.

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Liu, G., He, J., Dou, S. et al. Pretargeting in tumored mice with radiolabeled morpholino oligomer showing low kidney uptake. Eur J Nucl Med Mol Imaging 31, 417–424 (2004). https://doi.org/10.1007/s00259-003-1393-9

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  • DOI: https://doi.org/10.1007/s00259-003-1393-9

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