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系统分析 miR-506-3p 的靶基因鉴定其分化诱导功能的关键介质。

Systematic Analysis of miR-506-3p Target Genes Identified Key Mediators of Its Differentiation-Inducing Function.

机构信息

Department of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA.

出版信息

Genes (Basel). 2024 Sep 27;15(10):1268. doi: 10.3390/genes15101268.

Abstract

: miR-506-3p has been demonstrated to be a strong inducer of neuroblastoma cell differentiation, highlighting the potential of applying miR-506-3p mimics to neuroblastoma differentiation therapy. However, the target genes of miR-506-3p that mediate its differentiation-inducing function have not been fully defined. This study aims to comprehensively investigate the targetome of miR-506-3p regarding its role in regulating neuroblastoma cell differentiation. : We combined gene expression profiling and functional high-content screening (HCS) to identify miR-506-3p target genes that have differentiation-modulating functions. For evaluating the potential clinical relevance of the identified genes, we analyzed the correlations of gene expressions with neuroblastoma patient survival. : We identified a group of 19 target genes with their knockdown significantly inducing cell differentiation, suggesting that these genes play a key role in mediating the differentiation-inducing activity of miR-506-3p. We observed significant correlations of higher mRNA levels with lower patient survival with 13 of the 19 genes, suggesting that overexpression of these 13 genes plays important roles in promoting neuroblastoma development by disrupting the cell differentiation pathways. : Through this study, we identified novel target genes of miR-506-3p that function as strong modulators of neuroblastoma cell differentiation. Our findings represent a significant advancement in understanding the mechanisms by which miR-506-3p induces neuroblastoma cell differentiation. Future investigations of the identified 13 genes are needed to fully define their functions and mechanisms in controlling neuroblastoma cell differentiation, the understanding of which may reveal additional targets for developing novel differentiation therapeutic agents.

摘要

miR-506-3p 已被证明是强烈诱导神经母细胞瘤细胞分化的诱导物,突出了应用 miR-506-3p 模拟物进行神经母细胞瘤分化治疗的潜力。然而,miR-506-3p 介导其诱导分化功能的靶基因尚未完全确定。本研究旨在全面研究 miR-506-3p 在调节神经母细胞瘤细胞分化中的靶基因组。

我们结合基因表达谱和功能高内涵筛选(HCS)来鉴定 miR-506-3p 的靶基因,这些靶基因具有调节分化的功能。为了评估鉴定基因的潜在临床相关性,我们分析了基因表达与神经母细胞瘤患者生存的相关性。

我们鉴定了一组 19 个靶基因,它们的敲低显著诱导细胞分化,这表明这些基因在介导 miR-506-3p 的诱导分化活性中发挥关键作用。我们观察到 19 个基因中的 13 个基因的 mRNA 水平较高与患者生存率较低之间存在显著相关性,这表明这些 13 个基因的过表达通过破坏细胞分化途径在促进神经母细胞瘤发展中发挥重要作用。

通过这项研究,我们确定了 miR-506-3p 的新靶基因,这些靶基因作为神经母细胞瘤细胞分化的强烈调节剂。我们的发现代表了对 miR-506-3p 诱导神经母细胞瘤细胞分化机制的理解的重大进展。需要对鉴定的 13 个基因进行进一步研究,以充分定义它们在控制神经母细胞瘤细胞分化中的功能和机制,对这些基因的理解可能会揭示用于开发新型分化治疗剂的其他靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d43/11507652/911d9e469f6c/genes-15-01268-g001.jpg

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