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首页> 外文期刊>Pathology oncology research: POR >Research on the Typical miRNA and Target Genes in Squamous Cell Carcinoma and Adenocarcinoma of Esophagus Cancer with DNA Microarray
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Research on the Typical miRNA and Target Genes in Squamous Cell Carcinoma and Adenocarcinoma of Esophagus Cancer with DNA Microarray

机译:食管癌鳞状细胞癌和腺癌中典型miRNA和靶基因的DNA芯片研究

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To identify the typically expressed miRNAs in squamous cell carcinoma (SCC) and adenocarcinoma (ADC) of esophagus cancer and their target genes, and explore the related functions and pathways, providing potential biomarkers for esophageal carcinoma diagnosis and treatment. Gene expression profile GSE13937 was downloaded from Gene Expression Omnibus database which includes 152 samples, paired non-cancerous and cancerous, 44 SCC cases and 32 ADC cases; the differentially expressed miRNAs were identified with limma packages in R language after the data were normalized. Selected differentially expressed miRNAs were further analyzed using bioinformatics methods. Firstly, verified targets of miRNAs in two miRNA databases: miRecods and miRTarBase were integrated to select the targets genes of differentially expressed miRNAs. Next, String software was used to construct the target genes interaction network. Finally, function and pathway enrichment analysis of genes in the interaction network was carried out with Gestalt software. Up-regulated hsa-miR-21 and down-regulated hsa-miR-203 were identified by comparing normal and cancer tissue samples, and the targets genes regulated by these two miRNAs were most significantly related to cell cycle function and pathway, especially in the phase of G1/S. The two differentially expressed miRNA: hsa-miR-21 and hsa-miR-203 provide evidence for early diagnosis and treatment of esophageal carcinoma. The functions and pathways of target genes shows that deep understanding of cell cycle G1/S will help to illustrate the relationship between cell cycle regulation and pathogenesis of esophageal cancer.
机译:为了识别食管癌的鳞状细胞癌(SCC)和腺癌(ADC)中的典型表达miRNA及其靶基因,并探索相关的功能和途径,为食管癌的诊断和治疗提供潜在的生物标记。基因表达谱GSE13937是从基因表达综合数据库中下载的,该数据库包括152个样本,成对的非癌性和癌性,44例SCC病例和32例ADC病例;数据归一化后,用limma软件包以R语言识别差异表达的miRNA。使用生物信息学方法进一步分析选定的差异表达的miRNA。首先,在两个miRNA数据库中验证了miRNA的靶标:将miRecods和miRTarBase整合在一起,以选择差异表达的miRNA的靶标基因。接下来,使用String软件构建目标基因相互作用网络。最后,利用Gestalt软件进行了相互作用网络中基因的功能和途径富集分析。通过比较正常组织和癌组织样品,鉴定出上调的hsa-miR-21和下调的hsa-miR-203,这两种miRNA调控的靶基因与细胞周期功能和途径密切相关,尤其是在G1 / S的相位。两种差异表达的miRNA:hsa-miR-21和hsa-miR-203为食管癌的早期诊断和治疗提供了证据。靶基因的功能和途径表明,对细胞周期G1 / S的深入了解将有助于阐明细胞周期调控与食管癌发病机理之间的关系。

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