Review

A-to-I editing technologies: unlocking new avenues in cancer therapy

Number: 062 September 30, 2025

A-to-I editing technologies: unlocking new avenues in cancer therapy

Abstract

This review examines the critical role of adenosine-to-inosine (A-to-I) RNA editing in oncology, focusing on its molecular mechanisms, clinical relevance, and therapeutic applications. The ADAR family of enzymes mediates A-to-I editing, influencing RNA stability, translation efficiency, and immune modulation. Dysregulated ADAR activity has shown a relationship with multiple cancers, including glioma, hepatocellular carcinoma, and breast cancer. This review is structured into three main sections. First, we provide an overview of the mechanisms of RNA editing and its regulatory functions in cancer biology. Next, we highlight its clinical relevance, particularly how altered RNA editing contributes to oncogenesis and immune evasion. Finally, we explore therapeutic strategies, including ADAR inhibitors, antisense oligonucleotides (ASOs), and inosine-mediated RNA modifications to restore gene expression balance. Restoring ADAR function involves correcting RNA editing imbalances, particularly tumor cells' disrupted equilibrium between ADAR1 and ADAR2. This modulation can counteract oncogenic RNA changes and enhance immunotherapy efficacy. We also elaborate on the clinical applications of RNA editing in precision medicine, highlighting its potential to revolutionize cancer therapy. Unlike permanent genomic modifications, RNA editing provides a reversible and dynamic approach, making it an attractive strategy for targeted cancer interventions. Integrating RNA editing strategies into oncology and biomedical research could pave the way for new therapeutic advances.

Keywords

Supporting Institution

Hasret TURKMEN was supported by the Scientific and Technological Research Council of Turkey (TÜBİTAK) under project number[123C441]

Ethical Statement

This review did not involve human or animal subjects and therefore did not require ethical approval.

References

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Details

Primary Language

English

Subjects

Genomics and Transcriptomics, Medical Biochemistry - Nucleic Acids, Gene and Molecular Therapy

Journal Section

Review

Publication Date

September 30, 2025

Submission Date

February 18, 2025

Acceptance Date

March 24, 2025

Published in Issue

Year 2025 Number: 062

APA
Turkmen, H., Demir, N., Şen, M., & Can, M. (2025). A-to-I editing technologies: unlocking new avenues in cancer therapy. Journal of Scientific Reports-A, 062, 200-216. https://doi.org/10.59313/jsr-a.1642298
AMA
1.Turkmen H, Demir N, Şen M, Can M. A-to-I editing technologies: unlocking new avenues in cancer therapy. JSR-A. 2025;(062):200-216. doi:10.59313/jsr-a.1642298
Chicago
Turkmen, Hasret, Nefise Demir, Mustafa Şen, and Mustafa Can. 2025. “A-to-I Editing Technologies: Unlocking New Avenues in Cancer Therapy”. Journal of Scientific Reports-A, nos. 062: 200-216. https://doi.org/10.59313/jsr-a.1642298.
EndNote
Turkmen H, Demir N, Şen M, Can M (September 1, 2025) A-to-I editing technologies: unlocking new avenues in cancer therapy. Journal of Scientific Reports-A 062 200–216.
IEEE
[1]H. Turkmen, N. Demir, M. Şen, and M. Can, “A-to-I editing technologies: unlocking new avenues in cancer therapy”, JSR-A, no. 062, pp. 200–216, Sept. 2025, doi: 10.59313/jsr-a.1642298.
ISNAD
Turkmen, Hasret - Demir, Nefise - Şen, Mustafa - Can, Mustafa. “A-to-I Editing Technologies: Unlocking New Avenues in Cancer Therapy”. Journal of Scientific Reports-A. 062 (September 1, 2025): 200-216. https://doi.org/10.59313/jsr-a.1642298.
JAMA
1.Turkmen H, Demir N, Şen M, Can M. A-to-I editing technologies: unlocking new avenues in cancer therapy. JSR-A. 2025;:200–216.
MLA
Turkmen, Hasret, et al. “A-to-I Editing Technologies: Unlocking New Avenues in Cancer Therapy”. Journal of Scientific Reports-A, no. 062, Sept. 2025, pp. 200-16, doi:10.59313/jsr-a.1642298.
Vancouver
1.Hasret Turkmen, Nefise Demir, Mustafa Şen, Mustafa Can. A-to-I editing technologies: unlocking new avenues in cancer therapy. JSR-A. 2025 Sep. 1;(062):200-16. doi:10.59313/jsr-a.1642298