Development and classification of RNA aptamers for therapeutic purposes: an updated review with emphasis on cancer

Today, RNA aptamers are being considered promising theranostic tools against a wide variety of disorders. RNA aptamers can fold into complex shapes and bind to diverse nanostructures, macromolecules, cells, and viruses. It is possible to isolate RNA aptamers from a vast pool of nucleic acids via the...

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Veröffentlicht in:Molecular and cellular biochemistry 2023-07, Vol.478 (7), p.1573-1598
Hauptverfasser: Razlansari, Mahtab, Jafarinejad, Somayeh, rahdar, Abbas, Shirvaliloo, Milad, Arshad, Rabia, Fathi-Karkan, Sonia, Mirinejad, Shekoufeh, Sargazi, Saman, Sheervalilou, Roghayeh, Ajalli, Narges, Pandey, Sadanand
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Sprache:eng
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Zusammenfassung:Today, RNA aptamers are being considered promising theranostic tools against a wide variety of disorders. RNA aptamers can fold into complex shapes and bind to diverse nanostructures, macromolecules, cells, and viruses. It is possible to isolate RNA aptamers from a vast pool of nucleic acids via the Systematic Evolution of Ligands by Exponential Enrichment (SELEX) method. As therapeutics, aptamers have great potential because of their ability to bind to proteins and selectively limit their activities with negligible side effects. Several RNA aptamers with potential implications in cancer diagnosis are known to confer a great affinity for single-stranded DNA molecules, long non-coding RNAs, circulating tumor cells, vascular endothelial growth factors, and tissue and sera-derived exosomes in patients with different malignancies. Furthermore, clinical investigations have revealed the efficacy of RNA aptamer-based agents in imaging modalities. This review seeks to deliver new insights into the development, classification, nanomerization, and modification of RNA aptamers, as well as their applications in cancer theranostics. The aptamers’ mechanism of action and their interest to clinical trials as theranostic agents are also discussed. Graphical Abstract
ISSN:0300-8177
1573-4919
DOI:10.1007/s11010-022-04614-x