髓系白血病
RNA剪接
生物
小儿癌症
环状RNA
恶性肿瘤
计算生物学
基因
髓样
生物信息学
核糖核酸
癌症研究
遗传学
癌症
作者
Huiying Sun,Yangyang Xie,Xiaoyan Wu,Wenting Hu,Xiaoxiao Chen,Kefei Wu,Han Wang,Shuang Zhao,Qiaoqiao Shi,Xiang Wang,Bowen Cui,Wenyan Wu,Rongrong Fan,Jianan Rao,Ronghua Wang,Ying Wang,Ying Zhong,Hui Yu,Bin‐Bing S. Zhou,Shuhong Shen,Yu Liu
标识
DOI:10.1016/j.canlet.2024.216880
摘要
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.
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