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Datasets exploring putative lncRNA-miRNA-mRNA axes in breast cancer cell lines

机译:数据集在乳腺癌细胞系中探索推定的LNCRNA-miRNA-mRNA轴

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摘要

Long non-coding RNA (lncRNA)/microRNA (miRNA)/messenger RNA (mRNA) interactions regulate oncogenesis and tumour suppression in breast cancer. Oncogenic lncRNA/miRNA/mRNA axes may offer novel therapeutic targets; therefore, identifying such axes is a clinically relevant undertaking. To explore miRNAs regulated by oncogenic lncRNAs, we queried the NCBI Gene Expression Omnibus (GEO) database to find datasets that profiled gene expression changes upon lncRNA knockdown in breast cancer. We identified four microarray datasets that permitted our interrogation of genes regulated by lncRNAs LincK, LincIN, SPRY4-IT1 and {"type":"entrez-nucleotide","attrs":{"text":"AC009283.1","term_id":"5731414","term_text":"AC009283.1"}}AC009283.1. We specifically analysed changes in miRNA transcripts within these datasets to study miRNAs regulated by each of the four lncRNAs. We subsequently identified the predicted mRNA targets for these miRNAs to uncover possible lncRNA/miRNA/mRNAs axes in breast cancer. These axes may be candidates for future investigation of gene regulation in breast cancer.
机译:长非编码RNA(LNCRNA)/ microRNA(miRNA)/信使RNA(mRNA)相互作用调节乳腺癌的肿瘤生成和肿瘤抑制。致癌型LNCRNA / miRNA / mRNA轴可以提供新的治疗靶标;因此,识别这种轴是临床相关的承诺。为了探索由致癌的LNCRNA调节的miRNA,我们询问NCBI基因表达综合(GEO)数据库,以查找分类的数据集,即乳腺癌中LNCRNA敲低对LNCRNA敲低的改变。我们确定了四个微阵列数据集,允许我们对Lncrnas Linck,Lincin,Spry4-IT1和{“类型”(“entrez-nucleotide”,“attrs”的语言询问:“attrs”:{“text”:“Ac009283.1”,“Term_ID” “:”5731414“,”Term_Text“:”AC009283.1“}} AC009283.1。我们特别分析了这些数据集中的miRNA转录物的变化,以研究由四个LNCRNA中的每一个调节的miRNA。我们随后鉴定了这些miRNA的预测mRNA靶标以在乳腺癌中揭示可能的LNCRNA / miRNA / mRNA轴。这些轴可能是未来乳腺癌基因调控的候选者。

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