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首页> 外文期刊>Cellular Physiology and Biochemistry >Microarray Profiling of TGF-β1-Induced Long Non-Coding RNA Expression Patterns in Human Lung Bronchial Epithelial BEAS-2B Cells
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Microarray Profiling of TGF-β1-Induced Long Non-Coding RNA Expression Patterns in Human Lung Bronchial Epithelial BEAS-2B Cells

机译:TGF-β1诱导人肺支气管上皮BEAS-2B细胞中长非编码RNA表达模式的微阵列分析

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Background/Aims TGF-β1 mediated radiation-induced bystander effects (RIBE) have been linked with malignant transformation and tumorigenesis. However, the underlying mechanisms are not fully understood. Methods To reveal new molecules of regulatory functions in this process, lncRNA microarray was performed to profile both lncRNA and mRNA expression patterns in human lung bronchial epithelial BEAS-2B cells treated with TGF-β1 at a concentration measured in the medium conditioned by directly irradiated BEAS-2B cells. The potential functions of the differentially expressed lncRNAs were predicted by GO and KEGG pathway analyses of their co-expressed mRNAs. Cis- and trans-regulation of the lncRNAs were analyzed and the interaction networks were constructed using Cytoscape. qRT-PCR was conducted to validate the results of microarray profiling. CCK-8 assay was employed for functional validation of 3 identified lncRNAs. Results 224 lncRNAs were found to be dysregulated, among which 6 lncRNAs were chosen for expression validation by qRT-PCR assay. Pathway analyses showed that differentially expressed lncRNAs are highly correlated with cell proliferation, transformation, migration, etc. Trans-regulation analyses showed that the differentially expressed lncRNAs most likely participate in the pathways regulated by four transcriptional factors, FOS, STAT3, RAD21 and E2F1, which have been identified to be involved in the modulation of oncogenic transformation, cell cycle progression, genomic instability, etc. lnc-THEMIS-2 and lnc-ITGB6-4, predicted to be regulated by STAT3 and E2F1 respectively, were found to rescue the decrease of cell viability induced by TGF-β1 treatment. Conclusion Our findings suggest that the differentially expressed lncRNAs induced by TGF-β1 play crucial roles in the oncogenic transformation and tumorigenesis, which provide a better understanding of the underlying mechanisms related to tumorigensis induced by LD/LDR radiations.
机译:背景/目的TGF-β1介导的辐射诱导的旁观者效应(RIBE)与恶性转化和肿瘤发生有关。但是,尚未完全理解其基本机制。方法为了揭示在这一过程中调节功能的新分子,进行了lncRNA微阵列分析,以TGF-β1处理的人肺支气管上皮BEAS-2B细胞中的nccRNA和mRNA表达模式进行了分析,其浓度在直接照射BEAS条件下的培养基中测量-2B细胞。通过GO和KEGG通路共表达的mRNA预测了差异表达的lncRNA的潜在功能。分析了lncRNA的顺式和反式调节,并使用Cytoscape构建了相互作用网络。进行了qRT-PCR以验证微阵列分析的结果。 CCK-8分析用于3个已鉴定的lncRNA的功能验证。结果发现224个lncRNA表达失调,其中6个lncRNA经qRT-PCR检测表达验证。途径分析表明,差异表达的lncRNA与细胞增殖,转化,迁移等高度相关。反式调节分析表明,差异表达的lncRNA最有可能参与受四个转录因子FOS,STAT3,RAD21和E2F1调控的途径,已经确定它们参与了致癌转化的调控,细胞周期进程,基因组不稳定性等。发现预期分别受STAT3和E2F1调控的lnc-THEMIS-2和lnc-ITGB6-4可以挽救肿瘤的发生。 TGF-β1处理诱导的细胞活力降低。结论我们的发现表明,TGF-β1诱导的差异表达的lncRNA在致癌转化和肿瘤发生中起着关键作用,从而使人们更好地了解LD / LDR辐射诱导的与肿瘤相关的潜在机制。

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