# Advances in DNAzyme Selection, Molecular Engineering and Biomedical Applications

**Authors:** Li Yan, Jingjing Tian, Hongyu Yang, Shuai Liu, Zaihui Du, Chen Li, Hongtao Tian

PMC · DOI: 10.3390/ijms27041833 · 2026-02-14

## TL;DR

This paper reviews recent advances in DNAzyme development and their biomedical applications, focusing on improved design and clinical potential.

## Contribution

A novel conceptual framework for DNAzyme development integrating selection, engineering, and clinical application is introduced.

## Key findings

- A continuous iteration workflow improves DNAzyme performance in biological settings.
- Engineering strategies like XNA substitution and structure-guided design enhance stability and controllability.
- DNAzymes show promise in biosensing, imaging, and treating diseases like cancer and inflammation.

## Abstract

DNAzymes are catalytically active single-stranded DNAs that fold into metal-ion-assisted architectures to mediate diverse reactions. Addressing the performance gap in biological settings, we establish a novel conceptual framework based on a continuous iteration workflow of selection, enhancement, and application. This paradigm integrates selection constraints, molecular engineering, and clinical context into a unified cycle. We summarize the evolution of SELEX toward application-driven selection incorporating functional/environmental constraints, deep-sequencing-enabled high-throughput activity readouts, droplet compartmentalization and structure- and computation-guided design. We further consolidate engineering strategies to improve stability, kinetics and controllability, including 2′-sugar modifications and XNA substitution, backbone and nucleobase functionalization, arm and secondary-structure engineering for switchable or split architectures and multivalent organization on nanocarriers or nucleic acid scaffolds to enhance local concentration, protection and targeted delivery. Finally, we survey applications in ultrasensitive biosensing and portable diagnostics, activatable and multimodal in vivo imaging, and therapies for cancer, inflammatory diseases and airway disorders, and outline translational priorities: data-driven design, next-generation delivery, standardized safety/PK-PD evaluation and scalable manufacturing, ultimately for clinical and point-of-care deployment.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, MPRIP (myosin phosphatase Rho interacting protein) [NCBI Gene 23164] {aka M-RIP, MRIP, RHOIP3, RIP3, p116Rip}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, CMTR1 (cap methyltransferase 1) [NCBI Gene 23070] {aka FTSJD2, KIAA0082, MTr1, hMTr1}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}
- **Diseases:** COPD (MESH:D029424), hematologic tumor (MESH:D019337), airway disorders (MESH:D000402), inflammation (MESH:D007249), neurodegeneration (MESH:D019636), injury to (MESH:D014947), asthmatic (MESH:D013224), ophthalmic and (MESH:C535922), respiratory diseases (MESH:D012140), cancer (MESH:D009369), vascular lesions (MESH:D014652), asthma (MESH:D001249), breast cancer (MESH:D001943), neointimal hyperplasia (MESH:D006965), TB (MESH:D014390), infectious (MESH:D003141), rheumatoid arthritis (MESH:D001172), atherosclerosis (MESH:D050197), cardiovascular and metabolic diseases (MESH:D002318), infection (MESH:D007239), cytotoxicity (MESH:D064420), vascular injury (MESH:D057772)
- **Chemicals:** imidazole (MESH:C029899), amide (MESH:D000577), nucleotide (MESH:D009711), Li+ (MESH:D008094), V (MESH:D014639), oligonucleotide (MESH:D009841), iron oxide (MESH:C000499), Ce (MESH:D002563), Au (MESH:D006046), metal (MESH:D008670), PN/PG (MESH:C059200), Phosphate (MESH:D010710), PS (MESH:D010758), sugar (MESH:D000073893), triazole (MESH:D014230), AP (MESH:D000667), nucleosides (MESH:D009705), lipid (MESH:D008055), H (MESH:D006859), DMSO (MESH:D004121), S (MESH:D013455), 2'-OMe (-), oxime (MESH:D010091), Na+ (MESH:D012964), phosphoramidate (MESH:C011067), 1-MT (MESH:C525396), L-phenylalanine (MESH:D010649)
- **Species:** Human rhinovirus sp. (species) [taxon 169066], Homo sapiens (human, species) [taxon 9606]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940319/full.md

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Source: https://tomesphere.com/paper/PMC12940319