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Published in: Molecular Cancer 1/2019

Open Access 01-12-2019 | Letter to Editor

Genome-wide identification of cancer-specific alternative splicing in circRNA

Authors: Jing Feng, Ke Chen, Xin Dong, Xiaolong Xu, Yuxuan Jin, Xinyang Zhang, Wenbo Chen, Yujing Han, Lin Shao, Yang Gao, Chunjiang He

Published in: Molecular Cancer | Issue 1/2019

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Abstract

Circular RNA (circRNA) is a group of RNA families generated by RNA circularization, which was discovered ubiquitously across different cancers. However, the internal structure of circRNA is difficult to determine due to alternative splicing that occurs in its exons and introns. Furthermore, cancer-specific alternative splicing of circRNA is less likely to be identified. Here, we proposed a de novo algorithm, CircSplice, that could identify internal alternative splicing in circRNA and compare differential circRNA splicing events between different conditions (http://​gb.​whu.​edu.​cn/​CircSplice or https://​github.​com/​GeneFeng/​CircSplice). By applying CircSplice in clear cell renal cell carcinoma and bladder cancer, we detected 4498 and 2977 circRNA alternative splicing (circ-AS) events in the two datasets respectively and confirmed the expression of circ-AS events by RT-PCR. We further inspected the distributions and patterns of circ-AS in cancer and adjacent normal tissues. To further understand the potential functions of cancer-specific circ-AS, we classified those events into tumor suppressors and oncogenes and performed pathway enrichment analysis. This study is the first comprehensive view of cancer-specific circRNA alternative splicing, which could contribute significantly to regulation and functional research of circRNAs in cancers.
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Metadata
Title
Genome-wide identification of cancer-specific alternative splicing in circRNA
Authors
Jing Feng
Ke Chen
Xin Dong
Xiaolong Xu
Yuxuan Jin
Xinyang Zhang
Wenbo Chen
Yujing Han
Lin Shao
Yang Gao
Chunjiang He
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Molecular Cancer / Issue 1/2019
Electronic ISSN: 1476-4598
DOI
https://doi.org/10.1186/s12943-019-0996-0

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