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Updated: Jun 17, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
Adenosine-to-inosine RNA editing in cancer: molecular mechanisms and downstream targets
Hao Cheng1, Jun Yu1, Chi Chun Wong1
1Institute of Digestive Disease and Department of Medicine and Therapeutics, State Key Laboratory of Digestive Disease, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, SAR 518172, China.
Abstract:
Adenosine-to-inosine (A-to-I), one of the most prevalent RNA modifications, has recently garnered significant attention. The A-to-I modification actively contributes to biological and pathological processes by affecting the structure and function of various RNA molecules, including double-stranded RNA, transfer RNA, microRNA, and viral RNA. Increasing evidence suggests that A-to-I plays a crucial role in the development of human disease, particularly in cancer, and aberrant A-to-I levels are closely associated with tumorigenesis and progression through regulation of the expression of multiple oncogenes and tumor suppressor genes. Currently, the underlying molecular mechanisms of A-to-I modification in cancer are not comprehensively understood. Here, we review the latest advances regarding the A-to-I editing pathways implicated in cancer, describing their biological functions and their connections to the disease.
Insights
Adenosine-to-Inosine (A-to-I) RNA editing is vital in biological processes and disease, especially cancer. This review explores A-to-I pathways in cancer, their functions, and disease connections.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Adenosine-to-Inosine (A-to-I) RNA editing is a prevalent post-transcriptional modification impacting RNA structure and function.
- A-to-I editing influences diverse RNA types, including mRNA, tRNA, miRNA, and viral RNA, affecting biological and pathological processes.
- Aberrant A-to-I levels are linked to human diseases, particularly cancer, by regulating oncogenes and tumor suppressor genes.
Purpose of the Study:
- To review recent advancements in understanding A-to-I editing pathways in cancer.
- To elucidate the biological functions of A-to-I editing in the context of tumorigenesis and progression.
- To connect the molecular mechanisms of A-to-I modification to cancer development and progression.
Main Methods:
- Literature review of current research on A-to-I editing in cancer.
- Analysis of studies investigating the role of A-to-I editing enzymes and pathways.
- Synthesis of findings on the impact of A-to-I editing on gene expression in cancer.
Main Results:
- A-to-I editing significantly impacts cancer development and progression.
- Specific A-to-I editing events regulate key cancer-related genes.
- Dysregulation of A-to-I editing pathways contributes to oncogenesis.
Conclusions:
- A-to-I editing represents a critical layer of gene regulation in cancer.
- Further research into A-to-I editing mechanisms is essential for understanding cancer biology.
- Targeting A-to-I editing pathways may offer novel therapeutic strategies for cancer treatment.
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