The non-coding competing endogenous RNAs in acute myeloid leukemia: biological and clinical implications

竞争性内源性RNA 小RNA 髓系白血病 生物 假基因 计算生物学 长非编码RNA 生物标志物 环状RNA 非编码RNA 基因 核糖核酸 生物信息学 癌症研究 遗传学 基因组
作者
Qi Zhou,Xiaojun Shu,Yihong Chai,Wenjun Liu,Zijian Li,Yuandi Xi
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:163: 114807-114807 被引量:5
标识
DOI:10.1016/j.biopha.2023.114807
摘要

Acute myeloid leukemia (AML) is a hematologic carcinoma that has seen a considerable improvement in patient prognosis because of genetic diagnostics and molecularly-targeted therapies. Nevertheless, recurrence and drug resistance remain significant obstacles to leukemia treatment. It is critical to investigate the underlying molecular mechanisms and find solutions. Non-coding RNAs (ncRNAs), such as microRNAs (miRNAs), circular RNAs, long non-coding RNAs, and pseudogenes, have been found to be crucial components in driving cancer. The competing endogenous RNA (ceRNA) mechanism has expanded the complexity of miRNA-mediated gene regulation. A great deal of literature has shown that ncRNAs are essential to the biological functions of the ceRNA network (ceRNET). NcRNAs can compete for the same miRNA response elements to influence miRNA-target RNA interactions. Recent evidence suggests that ceRNA might be a potential biomarker and therapeutic strategy. So far, however, there have been no comprehensive studies on ceRNET about AML. What is not yet clear is the clinical application of ceRNA in AML. This study attempts to summarize the development of research on the related ceRNAs in AML and the roles of ncRNAs in ceRNET. We also briefly describe the mechanisms of ceRNA and ceRNET. What's more significant is that we explore the clinical value of ceRNAs to provide accurate diagnostic and prognostic biomarkers as well as therapeutic targets. Finally, limitations and prospects are considered.
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