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Updated: Jan 25, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
The Cancer Editome Atlas: A Resource for Exploratory Analysis of the Adenosine-to-Inosine RNA Editome in Cancer
Chui-Hsien Lin1, Sean Chun-Chang Chen2
1Graduate Institute of Biomedical Informatics, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Abstract:
Increasing evidence has suggested a role for adenosine-to-inosine RNA editing in carcinogenesis. However, the clinical utility of RNA editing remains limited because functions of the vast majority of editing events remain largely unexplored. To help the cancer research community investigate functional consequences of individual editing events, we have developed a user-friendly bioinformatic resource, The Cancer Editome Atlas (TCEA; http://tcea.tmu.edu.tw). TCEA characterizes >192 million editing events at >4.6 million editing sites from approximately 11,000 samples across 33 cancer types in The Cancer Genome Atlas. Clinical information, miRNA expression, and alteration in miRNA targeting modulated through RNA editing are also integrated into TCEA. TCEA supports several modules to search, analyze, and visualize the cancer editome, providing a solid basis for investigating the oncogenic mechanisms of RNA editing and expediting the identification of therapeutic targets in cancer. SIGNIFICANCE: This user-friendly bioinformatic resource reduces the barrier to analyzing the huge and complex cancer RNA editome that cancer researchers face and facilitates the identification of novel therapeutic targets in cancer.
Insights
Adenosine-to-inosine RNA editing plays a role in cancer. The Cancer Editome Atlas (TCEA) is a new resource to explore RNA editing events and identify potential cancer therapeutic targets.
Area of Science:
- Genomics
- Bioinformatics
- Cancer Research
Background:
- Adenosine-to-inosine RNA editing is increasingly implicated in cancer development.
- The functional roles of most RNA editing events are currently unknown, limiting clinical applications.
- Investigating RNA editing in cancer requires accessible tools to analyze large datasets.
Purpose of the Study:
- To develop a user-friendly bioinformatic resource for exploring the cancer RNA editome.
- To facilitate the investigation of functional consequences of RNA editing in carcinogenesis.
- To aid in the identification of novel therapeutic targets for cancer.
Main Methods:
- Development of The Cancer Editome Atlas (TCEA), a bioinformatic database.
- Characterization of over 192 million RNA editing events across 4.6 million sites.
- Integration of data from ~11,000 cancer samples across 33 cancer types from The Cancer Genome Atlas.
- Inclusion of clinical information and miRNA expression data, including RNA editing-modulated miRNA targeting.
Main Results:
- TCEA provides comprehensive characterization of the cancer RNA editome.
- The resource integrates diverse datasets, including clinical and miRNA information.
- TCEA offers modules for searching, analyzing, and visualizing RNA editing data.
Conclusions:
- TCEA significantly lowers the barrier for cancer researchers to analyze complex RNA editome data.
- This resource provides a foundation for understanding the oncogenic mechanisms of RNA editing.
- TCEA is expected to accelerate the discovery of new therapeutic strategies for cancer.
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