Abstract
AS1411, a 26-base guanine-rich oligonucleotide aptamer, has high affinity to nucleolin, mainly on tumor cell surfaces. In this study, a modified AS1411 was labeled with 99mTc and evaluated as a potential tumor-targeting agent for imaging. The AS1411 aptamer was conjugated with HYNIC and labeled with 99mTc in the presence a co-ligand. Radiochemical purity and stability testing of the 99mTc–HYNIC–AS1411 aptamer were carried out with thin layer chromatography and a size-exclusion column in normal saline and human serum. Cellular nucleolin-specific binding, cellular internalization in DU-145 cells, as high levels of nucleolin expression, were performed. Additionally, biodistribution in normal mice and DU-145 tumour-bearing mice was assessed. Radiolabeling of the aptamer resulted in a reasonable yield and radiochemical purity after purification. The aptamer was stable in normal saline and human serum, and cellular experiments demonstrated specific binding of the AS1411 aptamer to the nucleolin protein. Based on biodistribution assessment of 99mTc–HYNIC–AS1411, rapid blood clearance was seen after injection and it appears that the excretion route was via the urinary system at 1 h post-injection. Tumours also showed a higher accumulation of radioactivity with this labeled aptamer. 99mTc–AS1411 can be a potential tool for the molecular imaging of nucleolin-overexpressing cancers.
Declaration of interest
The authors declared no potential conflict of interest with respect to the authorship, and/or publication of this review.
This study was supported by a grant from Mazandaran University of Medical Sciences, Sari, Iran (ID#9217). This research was the subject of a PhD thesis of Zohreh Noaparast as a student of Mazandaran University of Medical Sciences.