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新型长链非编码RNA在儿童高超二倍体急性淋巴细胞白血病中的特异性表达

Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia.

作者信息

Lajoie Mathieu, Drouin Simon, Caron Maxime, St-Onge Pascal, Ouimet Manon, Gioia Romain, Lafond Marie-Hélène, Vidal Ramon, Richer Chantal, Oualkacha Karim, Droit Arnaud, Sinnett Daniel

机构信息

Division of Hematology-Oncology, Research Center, Sainte-Justine University Health Center, 3175 Chemin de la Côte-Sainte-Catherine, Montréal, QC, Canada.

Mathematics and Statistics Department, University of Quebec at Montreal (UQAM), 201 President-Kennedy Av., Montreal, QC, Canada.

出版信息

PLoS One. 2017 Mar 27;12(3):e0174124. doi: 10.1371/journal.pone.0174124. eCollection 2017.

DOI:10.1371/journal.pone.0174124
PMID:28346506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5367703/
Abstract

Pre-B cell childhood acute lymphoblastic leukemia (pre-B cALL) is a heterogeneous disease involving many subtypes typically stratified using a combination of cytogenetic and molecular-based assays. These methods, although widely used, rely on the presence of known chromosomal translocations, which is a limiting factor. There is therefore a need for robust, sensitive, and specific molecular biomarkers unaffected by such limitations that would allow better risk stratification and consequently better clinical outcome. In this study we performed a transcriptome analysis of 56 pre-B cALL patients to identify expression signatures in different subtypes. In both protein-coding and long non-coding RNAs (lncRNA), we identified subtype-specific gene signatures distinguishing pre-B cALL subtypes, particularly in t(12;21) and hyperdiploid cases. The genes up-regulated in pre-B cALL subtypes were enriched in bivalent chromatin marks in their promoters. LncRNAs is a new and under-studied class of transcripts. The subtype-specific nature of lncRNAs suggests they may be suitable clinical biomarkers to guide risk stratification and targeted therapies in pre-B cALL patients.

摘要

前B细胞型儿童急性淋巴细胞白血病(pre-B cALL)是一种异质性疾病,涉及许多亚型,通常使用细胞遗传学和基于分子的检测方法相结合进行分层。这些方法虽然被广泛使用,但依赖于已知染色体易位的存在,这是一个限制因素。因此,需要不受此类限制影响的强大、灵敏且特异的分子生物标志物,以实现更好的风险分层,从而获得更好的临床结果。在本研究中,我们对56例pre-B cALL患者进行了转录组分析,以确定不同亚型中的表达特征。在蛋白质编码和长链非编码RNA(lncRNA)中,我们都鉴定出了区分pre-B cALL亚型的亚型特异性基因特征,特别是在t(12;21)和超二倍体病例中。在pre-B cALL亚型中上调的基因在其启动子中富含二价染色质标记。lncRNAs是一类新的且研究较少的转录本。lncRNAs的亚型特异性表明它们可能是指导pre-B cALL患者风险分层和靶向治疗的合适临床生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e0/5367703/012a008725e5/pone.0174124.g009.jpg
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