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Updated: Mar 8, 2026

A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
Identification of Diverse Adenosine-to-Inosine RNA Editing Subtypes in Colorectal Cancer
Si-Hyun Lee1, Hwang-Phill Kim1,2, Jun-Kyu Kang1,2
1Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University College of Medicine, Seoul, Korea.
Purpose:
RNA editing generates protein diversity by altering RNA sequences in coding regions without changing the overall DNA sequence. Adenosine-to-inosine (A-to-I) RNA editing events have recently been reported in some types of cancer, but they are rare in human colorectal cancer (CRC). Therefore, this study was conducted to identify diverse RNA editing in CRC.
Materials And Methods:
We compared transcriptome data of 39 CRC samples and paired adjacent tissues from The Cancer Genome Atlas database to identify RNA editing patterns in CRC, focusing on canonical A-to-I RNA edits in coding sequence regions. We investigated nonsynonymous RNA editing patterns by comparing tumor and normal tissue transcriptome data.
Results:
The number of RNA edits varied from 12 to 42 per sample. We also observed that hypoand hyper-RNA editing patterns were distinguishable within the samples. We found 10 recurrent nonsynonymous RNA editing candidates in nine genes (PDLIM, NEIL1, SRP9, GLI1, APMAP, IGFBP7, ZNF358, COPA, and ZNF587B) and validated some by Sanger sequencing and the inosine chemical erasing assay. We further showed that editing at these positions was performed by the adenosine deaminase acting on RNA 1 enzyme. Most of these genes are hypoedited in CRC, but editing of GLI1 was increased in cancer tissues compared with normal tissues.
Conclusion:
Our results show that nonsynonymous RNA editing patterns can be used to identify CRC patients and could serve as novel biomarkers for CRC.
Insights
This study identified novel RNA editing patterns in colorectal cancer (CRC), revealing potential biomarkers for patient identification. Specific gene editing alterations were observed, distinguishing cancer from normal tissues.
Area of Science:
- Molecular Biology
- Genomics
- Cancer Research
Background:
- RNA editing diversifies proteins without altering DNA.
- Adenosine-to-inosine (A-to-I) RNA editing is rare in colorectal cancer (CRC).
Purpose of the Study:
- To identify diverse RNA editing patterns in human colorectal cancer (CRC).
- To investigate nonsynonymous RNA editing in CRC.
- To explore RNA editing as potential CRC biomarkers.
Main Methods:
- Compared transcriptome data from 39 CRC samples and adjacent tissues.
- Focused on canonical A-to-I RNA edits in coding regions.
- Analyzed nonsynonymous RNA editing patterns.
Main Results:
- Identified 10 recurrent nonsynonymous RNA editing candidates in nine genes.
- Observed both hypo- and hyper-RNA editing patterns in CRC samples.
- Found increased editing of GLI1 in cancer tissues, while most other genes were hypoedited.
Conclusions:
- Nonsynonymous RNA editing patterns can distinguish CRC patients.
- Identified RNA editing events may serve as novel biomarkers for CRC detection.
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