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骨髓增生异常综合征中长非编码 RNA 和 mRNA 表达谱的综合分析。

Integrated Analysis of Long Non-Coding RNA and mRNA Expression Profile in Myelodysplastic Syndromes.

出版信息

Clin Lab. 2020 May 1;66(5). doi: 10.7754/Clin.Lab.2019.190939.

DOI:10.7754/Clin.Lab.2019.190939
PMID:32390397
Abstract

BACKGROUND

Myelodysplastic syndromes (MDS) are a heterogeneous group of myeloid malignancies. The incidence of MDS is gradually increasing, but the pathogenesis is still not very clear. Studies have shown that long non-coding RNAs (lncRNAs) play a critical role in both oncogenic and tumor-suppressive pathways. However, the function of lncRNAs in MDS is still unknown. The purpose of this study was to investigate the expression profiles and biological function of the aberrantly expressed lncRNAs and mRNAs in MDS.

METHODS

We downloaded two data sets (GSE4619 and GSE19429) from the Gene Expression Omnibus database and obtained differentially expressed (DE) lncRNAs and DE-mRNAs between MDS cases and healthy controls. Then we performed systematic bioinformatics analysis to know the biological function of DE-lncRNAs and DE-mRNAs in MDS.

RESULTS

We identified 40 DE-lncRNAs and 643 DE-mRNAs between MDS cases and healthy controls. Gene Ontology (GO) and pathway analysis revealed that DE-lncRNAs and DE-mRNAs were mainly involved in necroptosis, apoptosis, immunodeficiency, p53 and FoxO signaling pathways. LncRNA-mRNA co-expression and lncRNA functional similarity network showed that twelve down-regulated lncRNAs co-regulated the same target gene and they were similar in function.

CONCLUSIONS

The comprehensive analysis of lncRNA and mRNA is helpful in understanding the pathogenesis of MDS, and the synergistically down-regulated lncRNAs may contribute to the development of new diagnostic and therapeutic strategies.

摘要

背景

骨髓增生异常综合征(MDS)是一组异质性髓系恶性肿瘤。MDS 的发病率逐渐增加,但发病机制尚不清楚。研究表明,长链非编码 RNA(lncRNA)在致癌和肿瘤抑制途径中都起着关键作用。然而,lncRNA 在 MDS 中的作用仍不清楚。本研究旨在探讨 MDS 中异常表达的 lncRNA 和 mRNA 的表达谱和生物学功能。

方法

我们从基因表达综合数据库中下载了两个数据集(GSE4619 和 GSE19429),并获得了 MDS 病例与健康对照之间差异表达的 lncRNA 和 DE-mRNA。然后,我们进行了系统的生物信息学分析,以了解 DE-lncRNA 和 DE-mRNA 在 MDS 中的生物学功能。

结果

我们在 MDS 病例与健康对照之间鉴定出 40 个 DE-lncRNA 和 643 个 DE-mRNA。GO 分析和通路分析表明,DE-lncRNA 和 DE-mRNA 主要参与了坏死性凋亡、细胞凋亡、免疫缺陷、p53 和 FoxO 信号通路。lncRNA-mRNA 共表达和 lncRNA 功能相似网络显示,12 个下调的 lncRNA 共同调控相同的靶基因,且功能相似。

结论

对 lncRNA 和 mRNA 的综合分析有助于理解 MDS 的发病机制,协同下调的 lncRNA 可能有助于新的诊断和治疗策略的发展。

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