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首页> 外文期刊>Cellular Physiology and Biochemistry >Profiles and Bioinformatics Analysis of Differentially Expressed Circrnas in Taxol-Resistant Non-Small Cell Lung Cancer Cells
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Profiles and Bioinformatics Analysis of Differentially Expressed Circrnas in Taxol-Resistant Non-Small Cell Lung Cancer Cells

机译:紫杉醇抗性非小细胞肺癌细胞中差异表达Circrnas的概况和生物信息学分析

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Background/Aims Circular RNAs (circRNAs) act as microRNA (miRNA) sponges that regulate gene expression and are involved in physiological and pathological processes. In this study, we evaluated the roles of circRNAs in the chemoresistance of non-small cell lung cancer (NSCLC) to taxol. Methods High-throughput circRNA microarrays were employed to investigate the circRNA profiles of parental A549 and taxol-resistant A549/Taxol cells. We predicted the miRNA targets of differentially expressed circRNAs via miRNA prediction software and then constructed a circRNA/miRNA network using Cytoscape. Bioinformatics analyses were performed to annotate dysregulated circRNAs in detail. Results We detected 2909 significantly upregulated and 8372 downregulated circRNAs in A549/Taxol cells compared with A549 cells. The circRNA/miRNA network displayed their interactions, suggesting that circRNAs exert biological effects by absorbing and sequestering miRNA molecules. Computational Gene Ontology and pathway analyses were used to determine the biological function and signaling pathways of host genes of dysregulated circRNAs and to identify potential molecular mechanisms prompting the resistance of NSCLC to taxol. Conclusion This study focusing on circRNAs related to taxol resistance provides a basis for clarifying the development and progression of drug resistance and for identifying therapeutic targets in NSCLC.
机译:背景/目的环状RNA(circRNA)充当调控基因表达并参与生理和病理过程的microRNA(miRNA)海绵。在这项研究中,我们评估了circRNA在非小细胞肺癌(NSCLC)对紫杉醇的化学耐药性中的作用。方法采用高通量circRNA微阵列技术研究亲本A549和耐紫杉醇A549 / Taxol细胞的circRNA谱。我们通过miRNA预测软件预测了差异表达circRNA的miRNA靶标,然后使用Cytoscape构建了circRNA / miRNA网络。进行了生物信息学分析以详细注释circRNA失调。结果与A549细胞相比,我们在A549 / Taxol细胞中检测到2909个circRNA显着上调和8372个下调的circRNA。 circRNA / miRNA网络显示出它们的相互作用,表明circRNA通过吸收和隔离miRNA分子发挥生物学作用。计算基因本体论和途径分析被用来确定失调的circRNAs宿主基因的生物学功能和信号传导途径,并确定促使NSCLC对紫杉醇耐药的潜在分子机制。结论这项针对与紫杉醇抗性相关的circRNA的研究为阐明抗药性的发展和进程以及确定NSCLC的治疗靶点提供了基础。

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