64Cu and fluorescein labeled anti-miRNA peptide nucleic acids for the detection of miRNA expression in living cells

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作者
Stefania Croci
Alex Manicardi
Sara Rubagotti
Martina Bonacini
Michele Iori
Pier Cesare Capponi
Gianfranco Cicoria
Maria Parmeggiani
Carlo Salvarani
Annibale Versari
Roberto Corradini
Mattia Asti
机构
[1] Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia,Clinical Immunology, Allergy, and Advanced Biotechnologies Unit, Diagnostic Imaging and Laboratory Medicine Department
[2] University of Parma,Department of Chemistry, Live Sciences and Environmental Sustainability
[3] Parco Area delle Scienze,Nuclear Medicine Unit, Oncology and Advanced Technologies Department
[4] Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia,Medical Physics Department
[5] University Hospital “S. Orsola-Malpighi”,Department of Surgery, Medicine, Dentistry and Morphological Sciences with interest in Transplant, Oncology and Regenerative Medicine
[6] Rheumatology Unit,Organic and Biomimetic Chemistry Research Group, Department of Organic Chemistry, Faculty of Science
[7] Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia,undefined
[8] University of Modena and Reggio Emilia,undefined
[9] Ghent University,undefined
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MiRNAs are single stranded RNAs of 18–22 nucleotides. They are promising diagnostic and prognostic markers for several pathologies including tumors, neurodegenerative, cardiovascular and autoimmune diseases. In the present work the development and characterization of anti-miRNA radiolabeled probes based on peptide nucleic acids (PNAs) for potential non-invasive molecular imaging in vivo of giant cell arteritis are described. MiR-146a and miR-146b-5p were selected as targets because they have been found up-regulated in this disease. Anti-miR and scramble PNAs were synthesized and linked to carboxyfluorescein or DOTA. DOTA-anti-miR PNAs were then labelled with copper-64 (64Cu) to function as non-invasive molecular imaging tools. The affinity of the probes for the targets was assessed in vitro by circular dichroism and melting temperature. Differential uptake of fluorescein and 64Cu labeled anti-miRNA probes was tested on BCPAP and A549 cell lines, expressing different levels of miR-146a and -146b-5p. The experiments showed that the anti-miR-146a PNAs were more effective than the anti-miR-146b-5p PNAs. Anti-miR-146a PNAs could bind both miR-146a and miR-146b-5p. The uptake of fluorescein and 64Cu labeled anti-miR-146a PNAs was higher than that of the negative control scramble PNAs in miRNA expressing cells in vitro. 64Cu-anti-miR-146a PNAs might be further investigated for non-invasive PET imaging of miR-146 overexpressing diseases.
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