Evidence map›Paper›PMID 41783898›Full record

ArticleMedical review (2021)2026

Ribozyme biotechnology: emerging opportunities for medical applications in the RNA therapeutics era.

Jingjing Zhang, Zhiqin Xi, Ming Zhao, Jie Bai, Zhenzhen Li, Xuelin Zhan, Ying Zhang, Yijin Liu

Abstract read
In one paragraph

Article in Medical review (2021), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jingjing ZhangState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Zhiqin XiState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Ming ZhaoState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Jie BaiState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Zhenzhen LiState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.
Xuelin ZhanChina Regional Research Centre, International Centre for Genetic Engineering and Biotechnology, Taizhou, China.
Ying ZhangSchool of Medicine, University of St Andrews, St Andrews, UK.
Yijin LiuState Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, China.ORCID https://orcid.org/0000-0002-3643-8683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-based medicines have transformed modern therapeutics, exemplified by the clinical success of small interfering RNAs (siRNAs), antisense oligonucleotides (ASOs), and mRNA vaccines. Small self-cleaving ribozymes - compact catalytic RNA species capable of programmable cleavage and ligation - were among the earliest RNA drugs explored, yet their progress was initially hindered by instability, nuclease degradation, inefficient intracellular delivery, and immune activation. In this Perspective, we discuss how recent technological convergence has revived their potential. Comparative genomics has uncovered new catalytic classes, including Twister, Pistol, Hatchet, and Hovlinc ribozymes, thereby expanding the catalytic repertoire. High-resolution structural and computational studies have elucidated their reaction architectures, while chemical modifications and advanced nanocarrier systems - such as DNA nanostructures, spherical nucleic acids, and lipid nanoparticles - have markedly improved molecular stability and delivery efficiency. Emerging applications, from ligand-responsive aptazymes and ribozyme-SNA conjugates to the StitchR RNA trans-ligation platform, further illustrate the expanding biomedical versatility of catalytic RNA. Together, these advances are redefining the role of ribozymes in oncology, virology, and genetic medicine. No longer a dormant concept, ribozymes now stand as an evolving frontier - rationally engineered catalysts that continue to inspire technological creativity and renewed optimism in RNA therapeutics.

Indexed as

catalytic RNAnucleic acid drugribozymeRNA therapeuticsStitchR platform

Identifiers

PMID41783898
PMCPMC12955351

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.