| Literature DB >> 30735636 |
Josh N Vo1, Marcin Cieslik1, Yajia Zhang1, Sudhanshu Shukla2, Lanbo Xiao3, Yuping Zhang3, Yi-Mi Wu3, Saravana M Dhanasekaran3, Carl G Engelke3, Xuhong Cao3, Dan R Robinson3, Alexey I Nesvizhskii4, Arul M Chinnaiyan5.
Abstract
Circular RNAs (circRNAs) are an intriguing class of RNA due to their covalently closed structure, high stability, and implicated roles in gene regulation. Here, we used an exome capture RNA sequencing protocol to detect and characterize circRNAs across >2,000 cancer samples. When compared against Ribo-Zero and RNase R, capture sequencing significantly enhanced the enrichment of circRNAs and preserved accurate circular-to-linear ratios. Using capture sequencing, we built the most comprehensive catalog of circRNA species to date: MiOncoCirc, the first database to be composed primarily of circRNAs directly detected in tumor tissues. Using MiOncoCirc, we identified candidate circRNAs to serve as biomarkers for prostate cancer and were able to detect circRNAs in urine. We further detected a novel class of circular transcripts, termed read-through circRNAs, that involved exons originating from different genes. MiOncoCirc will serve as a valuable resource for the development of circRNAs as diagnostic or therapeutic targets across cancer types.Entities:
Keywords: biomarkers; cancer; circRNA; circRNA database; exome capture sequencing; non-coding RNA; read-through transcripts
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Year: 2019 PMID: 30735636 PMCID: PMC6601354 DOI: 10.1016/j.cell.2018.12.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582