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Updated: Aug 12, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
The Integrative Studies on the Functional A-to-I RNA Editing Events in Human Cancers
Sijia Wu1, Zhiwei Fan2, Pora Kim3
1School of Life Science and Technology, Xidian University, Xi'an 710071, China.
Abstract:
Adenosine-to-inosine (A-to-I) RNA editing, constituting nearly 90% of all RNA editing events in humans, has been reported to contribute to the tumorigenesis in diverse cancers. However, the comprehensive map for functional A-to-I RNA editing events in cancers is still insufficient. To fill this gap, we systematically and intensively analyzed multiple tumorigenic mechanisms of A-to-I RNA editing events in samples across 33 cancer types from The Cancer Genome Atlas. For individual candidate among ∼ 1,500,000 quantified RNA editing events, we performed diverse types of downstream functional annotations. Finally, we identified 24,236 potentially functional A-to-I RNA editing events, including the cases in APOL1, IGFBP3, GRIA2, BLCAP, and miR-589-3p. These events might play crucial roles in the scenarios of tumorigenesis, due to their tumor-related editing frequencies or probable effects on altered expression profiles, protein functions, splicing patterns, and microRNA regulations of tumor genes. Our functional A-to-I RNA editing events (https://ccsm.uth.edu/CAeditome/) will help better understand the cancer pathology from the A-to-I RNA editing aspect.
Insights
This study maps functional Adenosine-to-inosine (A-to-I) RNA editing events in 33 cancer types. Researchers identified 24,236 events potentially impacting tumorigenesis, offering new insights into cancer pathology.
Area of Science:
- Genomics
- Molecular Biology
- Cancer Research
Background:
- Adenosine-to-inosine (A-to-I) RNA editing is prevalent in humans, implicated in cancer development.
- A comprehensive understanding of functional A-to-I RNA editing in cancers remains limited.
Purpose of the Study:
- To systematically analyze the tumorigenic mechanisms of A-to-I RNA editing events across diverse cancer types.
- To create a comprehensive map of functional A-to-I RNA editing events in cancer.
Main Methods:
- Analysis of A-to-I RNA editing events in samples from The Cancer Genome Atlas across 33 cancer types.
- Systematic functional annotation of approximately 1,500,000 quantified RNA editing events.
- Identification of potentially functional events based on editing frequencies and predicted impacts.
Main Results:
- Identification of 24,236 potentially functional A-to-I RNA editing events across 33 cancer types.
- Examples of identified events include those in APOL1, IGFBP3, GRIA2, BLCAP, and miR-589-3p.
- These events show potential roles in tumorigenesis through altered gene expression, protein function, splicing, and microRNA regulation.
Conclusions:
- The identified functional A-to-I RNA editing events offer crucial insights into cancer pathology.
- This resource aids in understanding the role of RNA editing in tumorigenesis.
- The findings provide a foundation for further research into A-to-I editing as a cancer biomarker or therapeutic target.
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