Development and classification of RNA aptamers for therapeutic purposes: an updated review with emphasis on cancer
- PMID: 36434145
- DOI: 10.1007/s11010-022-04614-x
Development and classification of RNA aptamers for therapeutic purposes: an updated review with emphasis on cancer
Abstract
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.
Keywords: Aptamers; Cancer; Diagnostics; Drug delivery; Imaging; Nucleic acid; RNA; SELEX.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Similar articles
-
Chimeric aptamers in cancer cell-targeted drug delivery.Crit Rev Biochem Mol Biol. 2011 Dec;46(6):459-77. doi: 10.3109/10409238.2011.614592. Epub 2011 Sep 28. Crit Rev Biochem Mol Biol. 2011. PMID: 21955150 Free PMC article. Review.
-
Nucleic Acid Aptamers as Emerging Tools for Diagnostics and Theranostics.Methods Mol Biol. 2019;2054:201-221. doi: 10.1007/978-1-4939-9769-5_14. Methods Mol Biol. 2019. PMID: 31482458
-
DNA and RNA aptamers: from tools for basic research towards therapeutic applications.Comb Chem High Throughput Screen. 2006 Sep;9(8):619-32. doi: 10.2174/138620706778249695. Comb Chem High Throughput Screen. 2006. PMID: 17017882 Review.
-
DNA and RNA aptamers as modulators of protein function.Med Chem. 2005 Mar;1(2):199-208. doi: 10.2174/1573406053175274. Med Chem. 2005. PMID: 16787315 Review.
-
Selection and Application of Aptamers and Intramers.Adv Exp Med Biol. 2016;917:241-58. doi: 10.1007/978-3-319-32805-8_11. Adv Exp Med Biol. 2016. PMID: 27236559 Review.
Cited by
-
Targeted self-assembled anti-NFκB AuNCs-aptamer nanoplatform for precise theranostics via tailored follicle regeneration.Mater Today Bio. 2025 Apr 17;32:101774. doi: 10.1016/j.mtbio.2025.101774. eCollection 2025 Jun. Mater Today Bio. 2025. PMID: 40290889 Free PMC article.
-
Aptamer-targeted anti-miR RNA construct based on 3WJ as a new approach for the treatment of chronic kidney disease in an experimental model.Gene Ther. 2025 Jul;32(4):359-375. doi: 10.1038/s41434-025-00544-7. Epub 2025 Jun 14. Gene Ther. 2025. PMID: 40514411 Free PMC article.
-
Aptamers' Potential to Fill Therapeutic and Diagnostic Gaps.Pharmaceuticals (Basel). 2024 Jan 12;17(1):105. doi: 10.3390/ph17010105. Pharmaceuticals (Basel). 2024. PMID: 38256938 Free PMC article.
-
Potential roles of FGF5 as a candidate therapeutic target in prostate cancer.Am J Clin Exp Urol. 2023 Dec 15;11(6):452-466. eCollection 2023. Am J Clin Exp Urol. 2023. PMID: 38148937 Free PMC article. Review.
-
Targeting lncRNAs of colorectal cancers with natural products.Front Pharmacol. 2023 Jan 9;13:1050032. doi: 10.3389/fphar.2022.1050032. eCollection 2022. Front Pharmacol. 2023. PMID: 36699052 Free PMC article. Review.
References
-
- Hathout L et al (2021) A multi-institutional analysis of adjuvant chemotherapy and radiation sequence in women with stage IIIC endometrial cancer. IntJ Radiat Oncol Biol Phys 110(5):1423–1431 - DOI
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials