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A New Network-Based Strategy for Predicting the Potential miRNA-mRNA Interactions in Tumorigenesis

机译:一种新的基于网络的基于网络,用于预测肿瘤发生中的潜在miRNA-mRNA相互作用

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摘要

MicroRNA (miRNA) plays an important role in the degradation and inhibition of mRNAs and is a kind of essential drugtargets for cancer therapy. To facilitate the clinical cancer research, we proposed a network-based strategy to identify thecancer-related miRNAs and to predict their targeted genes based on the gene expression profiles. The strategy wasvalidated by using the data sets of acute myeloid leukemia (AML), breast invasive carcinoma (BRCA), and kidney renalclear cell carcinoma (KIRC). The results showed that in the top 20 miRNAs ranked by their degrees, 90.0% (18/20),70.0% (14/20), and 70.0% (14/20) miRNAs were found to be associated with the cancers for AML, BRCA, and KIRC,respectively. The KEGG pathways and GO terms enriched with the genes that were predicted as the targets of thecancer-related miRNAs were significantly associated with the biological processes of cancers. In addition, several genes,which were predicted to be regulated by more than three miRNAs, were identified to be the potential drug targetsannotated by using the human protein atlas database. Our results demonstrated that the proposed strategy can behelpful for predicting the miRNA-mRNA interactions in tumorigenesis and identifying the cancer-related miRNAs as thepotential drug targets.
机译:microRNA(miRNA)在降解和抑制mRNA的下降和抑制中起着重要作用,并且是一种癌症治疗的必需药物靶标。为了促进临床癌症研究,我们提出了一种基于网络的策略来鉴定与基于基因表达谱的基于网络相关的miRNA并预测其靶向基因。通过使用急性髓白血病(AML),乳房侵入性癌(BRCA)和肾肾素细胞癌(KIRC)的数据集来获得该策略。结果表明,在其度的前20位miRNA中,90.0%(18/20),70.0%(14/20)和70.0%(14/20)miRNA与AML的癌症相关, BRCA和KIRC分别。富含基因的KEGG途径和致力于预测的基因,作为脑癌相关的miRNA的靶标显着与癌症的生物学过程有关。此外,预计由三种以上的miRNA调节的几个基因被鉴定为通过使用人蛋白质阿特拉斯数据库是潜在的药物靶向。我们的研究结果表明,该策略可以注意到预测肿瘤发生中的miRNA-mRNA相互作用,并将与癌症相关的miRNA鉴定为如此的药物靶标。

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