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MicroRNAs-mRNAs Expression Profile and Their Potential Role in Malignant Transformation of Human Bronchial Epithelial Cells Induced by Cadmium

机译:Micrornas-mRNA表达谱及其在镉诱导的人支气管上皮细胞恶性转化中的潜在作用

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摘要

Background. Our study was designed to elucidate whether there were miRNA and mRNA aberrantly expression profiles and potential role in malignant transformation of 16HBE induced by Cd. Methods. mRNA and miRNA expression profiles were determined in 35th Cd-induced 16HBE and untreated 16HBE by microarray. A series of bioinformatics analyses such as predicting targets, GO, KEGG were performed to find DEGs, coexpressing networks between miRNAs and mRNAs and its functions. Results. 498 DEGs were found. 8 Cd-responsive novel miRNAs predicted previously were identified, and 5 of them were downregulated. 214 target genes were predicted for the Cd-responsive miRNAs, many of which appeared to regulate gene networks. Target gene CCM2 was showed reciprocal effect by miRNAs. According to the combination analysis, hsa-miR-27b-3p regulated most of the mRNAs, especially upregulated expression genes. The differentially expressed miRNAs are involved in the biological processes and channels, and these GO and KEGG enrichment analyses result were significantly enriched in the Cd-responsive. Discussion. These results provided a tight link for the miRNA-mRNA integrated network and implied the role of novel miRNAs in malignant transformation of 16HBE induced by Cadmium. It is better to understand the novel molecular mechanism of cadmium-induced tumorigenesis.
机译:背景。我们的研究旨在阐明是否存在miRNA和mRNA异常表达谱和CD诱导16HBE的恶性转化中的潜在作用。方法。 MRNA和miRNA表达谱在第35℃诱导16HBE和通过微阵列未经处理的16HBE测定。进行一系列生物信息学分析,例如预测目标,GO,KEGG,以查找米斯纳斯和MRNA之间的DEG,共存及其功能。结果。发现了498次。先前预测的8个响应响应的新型miRNA,其中5个被下调。预测CD响应MiRNA的214靶基因,其中许多似乎调节基因网络。靶基因CCM2通过MIRNA显示相互作用。根据组合分析,HSA-MIR-27B-3P调节大部分MRNA,尤其是上调的表达基因。差异表达的miRNA参与生物过程和通道,并且这些GO和KEGG富集分析结果在CD响应中显着富集。讨论。这些结果为miRNA-mRNA集成网络提供了紧密的链接,并暗示了小型miRNA在镉诱导16Hbe的恶性转化中的作用。更好地理解镉诱导的肿瘤发生的新分子机制。

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