Long noncoding RNA expression in acute lymphoblastic leukemia: A systematic review

被引:0
作者
Lobo-Alves, Sara Cristina [1 ,2 ,3 ,4 ]
de Oliveira, Liana Alves [1 ,3 ]
Kretzschmar, Gabriela Canalli [1 ,2 ,3 ]
Valengo, Andressa Eloisa [1 ,2 ]
Rosati, Roberto [1 ,2 ,3 ]
机构
[1] Inst Pesquisa Pele Pequeno Principe, Av Silva Jardim 1632, BR-80250060 Curitiba, PR, Brazil
[2] Fac Pequeno Principe, Av Iguacu 333, BR-80230020 Curitiba, PR, Brazil
[3] Natl Sci & Technol Inst Childrens Canc Biol & Pedi, BR-90035003 Porto Alegre, RS, Brazil
[4] Av Silva Jardim 1632, BR-80250060 Curitiba, PR, Brazil
关键词
Long noncoding RNA; Noncoding RNA; Acute lymphoblastic leukemia; Leukemia; Differential gene expression; Transcriptome; LINC01013; CRNDE; VARIANT TRANSLOCATION 1; CELL-PROLIFERATION; DOWN-REGULATION; LNCRNA; PROGRESSION; CHILDHOOD; CANCER; BIOMARKER; PROMOTES; PROGNOSIS;
D O I
10.1016/j.critrevonc.2024.104290
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Long noncoding RNAs (lncRNAs), as gene expression modulators, are potential players in Acute Lymphoblastic Leukemia (ALL) pathogenesis. We systematically explored current literature on lncRNA expression in ALL to identify lncRNAs consistently reported as differentially expressed (DE) either in ALL versus controls or between ALL subtypes. By comparing articles that provided global expression data for DE lncRNAs in the ETV6::RUNX1- positive ALL subtype, we identified four DE lncRNAs in three independent studies (two versus other subtypes and one versus controls), showing concordant expression of LINC01013, CRNDE and lnc-KLF7-1. Additionally, LINC01503 was consistently downregulated on ALL versus controls. Within RT-qPCR studies, twelve lncRNA were DE in more than one source. Thus, several lncRNAs were supported as DE in ALL by multiple sources, highlighting their potential role as candidate biomarkers or therapeutic targets. Finally, as lncRNA annotation is rapidly expanding, standardization of reporting and nomenclature is urgently needed to improve data verifiability and compilation.
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页数:20
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