Potential of miRNA as Imaging Targets for PET

被引:1
作者
Zientek, Simon H. [1 ]
Thompson, Stephen [1 ]
Aigbirhio, Franklin I. [1 ]
Sephton, Selena Milicevic [1 ]
机构
[1] Univ Cambridge, Dept Clin Neurosci, Mol Imaging Chem Lab, Cambridge Biomed Campus,West Forvie Bldg, Cambridge CB2 0SZ, England
关键词
miRNA; PET imaging; neuroinflammation; TSPO; radiolabelling; MICRORNA BINDING DOMAIN; 18 KDA TSPO; OPTIMIZED PREPARATION; OLIGONUCLEOTIDE; BIOGENESIS; MECHANISM; DELIVERY; IMPROVES; RNA;
D O I
10.1002/hlca.202400014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Positron Emission Tomography (PET) is an important part of the medical imaging field which is continually exploring novel biological targets as exemplified by PET imaging of neuroinflammation. Due to limitations stemming from either sub-optimal biological targets or a lack of available selective radiotracers, alternative biomarkers and PET imaging agent candidates are considered. One such possible target is microRNA (miRNA) and herein, we discuss the potential of miRNA for PET imaging. With the aim of addressing key strategies for imaging miRNA with PET, we identify three distinct approaches as follows: small molecules directly targeting miRNA, small molecules indirectly targeting Argonaute 2 (AGO2)-protein complexes, and direct chemical modification of antisense oligonucleotides. The radiosynthetic approaches are based on the methods of direct radiolabelling of respective antisense oligonucleotides and several examples are described herein, showcasing the potential of miRNA in PET imaging. Whilst these approaches offer different radiolabelling strategies, application of these radiolabelled molecules towards PET imaging of miRNA are scarce with only one, limited example applied to bone remodeling reported in the literature. image
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页数:18
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