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circRNAs as prognostic markers in pediatric acute myeloid leukemia.

Authors :
Sun H
Xie Y
Wu X
Hu W
Chen X
Wu K
Wang H
Zhao S
Shi Q
Wang X
Cui B
Wu W
Fan R
Rao J
Wang R
Wang Y
Zhong Y
Yu H
Zhou BS
Shen S
Liu Y
Source :
Cancer letters [Cancer Lett] 2024 Jun 01; Vol. 591, pp. 216880. Date of Electronic Publication: 2024 Apr 15.
Publication Year :
2024

Abstract

Circular RNAs (circRNAs) arise from precursor mRNA processing through back-splicing and have been increasingly recognized for their functions in various cancers including acute myeloid leukemia (AML). However, the prognostic implications of circRNA in AML remain unclear. We conducted a comprehensive genome-wide analysis of circRNAs using RNA-seq data in pediatric AML. We revealed a group of circRNAs associated with inferior outcomes, exerting effects on cancer-related pathways. Several of these circRNAs were transcribed directly from genes with established functions in AML, such as circRUNX1, circWHSC1, and circFLT3. Further investigations indicated the increased number of circRNAs and linear RNAs splicing were significantly correlated with inferior clinical outcomes, highlighting the pivotal role of splicing dysregulation. Subsequent analysis identified a group of upregulated RNA binding proteins in AMLs associated with high number of circRNAs, with TROVE2 being a prominent candidate, suggesting their involvement in circRNA associated prognosis. Through the integration of drug sensitivity data, we pinpointed 25 drugs that could target high-risk AMLs characterized by aberrant circRNA transcription. These findings underscore prognostic significance of circRNAs in pediatric AML and offer an alternative perspective for treating high-risk cases in this malignancy.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-7980
Volume :
591
Database :
MEDLINE
Journal :
Cancer letters
Publication Type :
Academic Journal
Accession number :
38621457
Full Text :
https://doi.org/10.1016/j.canlet.2024.216880