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与髓母细胞瘤4型亚组相关的微小RNA-信使核糖核酸表达谱

MicroRNA-mRNA expression profiles associated with medulloblastoma subgroup 4.

作者信息

Gershanov Sivan, Toledano Helen, Michowiz Shalom, Barinfeld Orit, Pinhasov Albert, Goldenberg-Cohen Nitza, Salmon-Divon Mali

机构信息

Genomic Bioinformatics Laboratory, Department of Molecular Biology, Ariel University, Ariel, Israel.

Department of Pediatric Oncology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.

出版信息

Cancer Manag Res. 2018 Feb 16;10:339-352. doi: 10.2147/CMAR.S156709. eCollection 2018.

Abstract

PURPOSE

Medulloblastoma (MB), the most common malignant brain tumor in children, is divided into four tumor subgroups: wingless-type (WNT), sonic hedgehog (SHH), Group 3, and Group 4. Ideally, clinical practice and treatment design should be subgroup specific. While WNT and SHH subgroups have well-defined biomarkers, distinguishing Group 3 from Group 4 is not straightforward. MicroRNAs (miRNAs), which regulate posttranscriptional gene expression, are involved in MB tumorigenesis. However, the miRNA-messenger RNA (mRNA) regulatory network in MB is far from being fully understood. Our aims were to investigate miRNA expression regulation in MB subgroups, to assess miRNA target relationships, and to identify miRNAs that can distinguish Group 3 from Group 4.

PATIENTS AND METHODS

With these aims, integrated transcriptome mRNA and miRNA expression analysis was performed on primary tumor samples collected from 18 children with MB, using miRNA sequencing (miRNA-seq), RNA sequencing (RNA-seq), and quantitative PCR.

RESULTS

Of all the expressed miRNAs, 19 appeared to be significantly differentially expressed (DE) between Group 4 and non-Group 4 subgroups (false discovery rate [FDR] <0.05), including 10 miRNAs, which, for the first time, are reported to be in conjunction with MB. RNA-seq analysis identified 165 genes that were DE between Group 4 and the other subgroups (FDR <0.05), among which seven are predicted targets of five DE miRNAs and exhibit inverse expression pattern.

CONCLUSION

This study identified miRNA molecules that may be involved in Group 4 etiology, in general, and can distinguish between Group 3 and Group 4, in particular. In addition, understanding the involvement of miRNAs and their targets in MB may improve diagnosis and advance the development of targeted treatment for MB.

摘要

目的

髓母细胞瘤(MB)是儿童最常见的恶性脑肿瘤,分为四个肿瘤亚组:无翼型(WNT)、音猬因子(SHH)、3组和4组。理想情况下,临床实践和治疗设计应针对亚组。虽然WNT和SHH亚组有明确的生物标志物,但区分3组和4组并不简单。微小RNA(miRNA)可调节转录后基因表达,参与MB的肿瘤发生。然而,MB中的miRNA-信使核糖核酸(mRNA)调控网络远未被完全理解。我们的目的是研究MB亚组中miRNA的表达调控,评估miRNA与靶标的关系,并鉴定可区分3组和4组的miRNA。

患者和方法

为实现这些目标,我们对18例MB患儿的原发性肿瘤样本进行了转录组mRNA和miRNA表达的综合分析,采用了miRNA测序(miRNA-seq)、RNA测序(RNA-seq)和定量PCR技术。

结果

在所有表达的miRNA中,有19种在4组和非4组亚组之间表现出显著差异表达(错误发现率[FDR]<0.05),其中10种miRNA首次被报道与MB相关。RNA-seq分析确定了165个在4组和其他亚组之间差异表达的基因(FDR<0.05),其中7个是5种差异表达miRNA的预测靶标,并呈现出相反的表达模式。

结论

本研究鉴定出了可能参与4组病因,特别是可区分3组和4组的miRNA分子。此外,了解miRNA及其靶标在MB中的作用可能会改善诊断并推动MB靶向治疗的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9627/5818864/a136a8754875/cmar-10-339Fig1.jpg

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