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生物信息学分析结合微阵列技术鉴定口腔癌中失调的微小RNA。

Bioinformatics analyses combined microarray identify the deregulated microRNAs in oral cancer.

作者信息

Cui Jing, Li Dalu, Zhang Wenmei, Shen Liang, Xu Xin

机构信息

Department of Oral and Maxillofacial Surgery, Jinan Stomatologic Hospital, Jinan, Shandong 250010, P.R. China ; School of Stomatology, Shandong University, Jinan, Shandong 250010, P.R. China.

Department of Oral Surgery, Jinan Stomatological Hospital, Jinan, Shandong 250010, P.R. China.

出版信息

Oncol Lett. 2014 Jul;8(1):218-222. doi: 10.3892/ol.2014.2070. Epub 2014 Apr 15.

Abstract

MicroRNAs (miRNAs) are important in the regulation of cell growth, differentiation, apoptosis and carcinogenesis. The overexpression of oncogenic miRNAs or the underexpression of tumor suppressor miRNAs exhibits a critical function in the tumorigenesis of oral cancer. The aim of the present study was to identify differentially expressed miRNAs (DE-miRNAs), which may differentiate oral cancer from normal tissues, as well as the molecular signatures that differ in tumor histology. The miRNA expression profiles of GSE28100 [the Gene Expression Omnibus (GEO) accession number] were downloaded from the GEO database and an independent sample t-test was used to identify statistical differences between the DE-miRNAs of the oral cancer patients and the healthy control subjects. The target genes of DE-miRNA were retrieved from the miRecords database. Furthermore, a protein-protein interaction network was constructed using the Search Tools for the Retrieval of Interacting Genes database and Cytoscape software. A total of 15 DE-miRNAs were identified and among them, hsa-miR-15a drew specific attention. Gene Ontology analysis revealed that the target genes of fibroblast growth factor (FGF)2 are involved in the progression of oral cancer. Furthermore, functional analysis indicated that the FGF-receptor signaling pathway was significantly upregulated in oral cancer. hsa-miR-15a is important in the regulation of oral cancer and thus, may present a potential biomarker for the prediction of oral cancer progression.

摘要

微小RNA(miRNA)在细胞生长、分化、凋亡和致癌过程的调控中发挥着重要作用。致癌性miRNA的过表达或肿瘤抑制性miRNA的低表达在口腔癌的发生发展中起着关键作用。本研究的目的是鉴定可能区分口腔癌与正常组织的差异表达miRNA(DE-miRNA),以及在肿瘤组织学上存在差异的分子特征。从基因表达综合数据库(GEO)下载GSE28100(GEO登录号)的miRNA表达谱,并使用独立样本t检验来确定口腔癌患者和健康对照受试者的DE-miRNA之间的统计学差异。从miRecords数据库中检索DE-miRNA的靶基因。此外,使用检索相互作用基因的搜索工具数据库和Cytoscape软件构建蛋白质-蛋白质相互作用网络。共鉴定出15种DE-miRNA,其中hsa-miR-15a引起了特别关注。基因本体分析显示,成纤维细胞生长因子(FGF)2的靶基因参与口腔癌的进展。此外,功能分析表明FGF受体信号通路在口腔癌中显著上调。hsa-miR-15a在口腔癌的调控中具有重要作用,因此可能是预测口腔癌进展的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e0/4063566/f92163fea14d/OL-08-01-0218-g00.jpg

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