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Review
. 2024 Sep;24(9):597-613.
doi: 10.1038/s41568-024-00721-7. Epub 2024 Jul 29.

Circular RNA in cancer

Affiliations
Review

Circular RNA in cancer

Vanessa M Conn et al. Nat Rev Cancer. 2024 Sep.

Abstract

Over the past decade, circular RNA (circRNA) research has evolved into a bona fide research field shedding light on the functional consequence of this unique family of RNA molecules in cancer. Although the method of formation and the abundance of circRNAs can differ from their cognate linear mRNA, the spectrum of interacting partners and their resultant cellular functions in oncogenesis are analogous. However, with 10 times more diversity in circRNA variants compared with linear RNA variants, combined with their hyperstability in the cell, circRNAs are equipped to influence every stage of oncogenesis. This is an opportune time to address the breadth of circRNA in cancer focused on their spatiotemporal expression, mutations in biogenesis factors and contemporary functions through each stage of cancer. In this Review, we highlight examples of functional circRNAs in specific cancers, which satisfy critical criteria, including their physical co-association with the target and circRNA abundance at stoichiometrically valid quantities. These considerations are essential to develop strategies for the therapeutic exploitation of circRNAs as biomarkers and targeted anticancer agents.

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References

    1. Yoshida, K. et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 478, 64–69 (2011). - PubMed - DOI
    1. Seiler, M. et al. Somatic mutational landscape of splicing factor genes and their functional consequences across 33 cancer types. Cell Rep. 23, 282–296.e4 (2018). - PubMed - PMC - DOI
    1. Suzuki, H. et al. Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma. Nature 574, 707–711 (2019). - PubMed - PMC - DOI
    1. Shuai, S. et al. The U1 spliceosomal RNA is recurrently mutated in multiple cancers. Nature 574, 712–716 (2019). - PubMed - DOI
    1. Wedge, E. et al. Impact of U2AF1 mutations on circular RNA expression in myelodysplastic neoplasms. Leukemia 37, 1113–1125 (2023). - PubMed - DOI

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