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Identification of NMU as a potential gene conferring alectinib resistance in non-small cell lung cancer based on bioinformatics analyses

机译:基于生物信息学分析的基于生物信息学分析,鉴定NMU作为赋予非小细胞肺癌壁肺抗性的潜在基因

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Non-small cell lung cancer (NSCLC) is the most common type of lung cancer, and adjuvant targeted therapy has shown great benefits for the NSCLC patients with specific genomic mutations. Alectinib, a selective anaplastic lymphoma kinase (ALK) inhibitor, has been clinically used for the NSCLC patients with ALK-rearrangement, however, irreversible therapeutic resistance for the patients receiving alectinib treatment frequently occurs. Here we show that neuromedin U (NMU) may confer the alectinib resistance in NSCLC via multiple mechanisms based on the integrative bioinformatics analyses. Through employing the bioinformatics analyses of three microarray datasets, NMU, overexpressed in both NSCLC tissues and alectinib-resistant NSCLC cells, was initially identified as potential candidate for causing alectinib resistance in NSCLC. The resistance function of NMU in NSCLC was validated by performing protein/gene interactions and biological process annotation analyses, and further validated by analyzing the transcription factors targeting NMU mRNA. Collectively, these results indicated that NMU may confer alectinib resistance in NSCLC.
机译:非小细胞肺癌(NSCLC)是最常见的肺癌类型,辅助靶向治疗对NSCLC患者具有很大的益处,具有特异性基因组突变。邻接肺鞘,一种选择性内塑性淋巴瘤激酶(ALK)抑制剂已被临床上用于NSCLC患者,然而,常常发生接受壁鞘治疗的患者的不可逆治疗抗性。在这里,我们表明,神经细胞素U(NMU)可以通过基于整合生物信息学分析通过多种机制赋予NSCLC中的焊接素抗性。通过采用三种微阵列数据集的生物信息学分析,NMU在NSCLC组织和抗渗润的NMSCLC细胞中过表达,最初被鉴定为导致NSCLC中的焊接素抗性的潜在候选物。通过进行蛋白质/基因相互作用和生物过程注释分析,通过分析靶向NMU mRNA的转录因子来验证NMU在NMSCC中的抗性函数。总的来说,这些结果表明NMU可以在NSCLC中赋予邻苯硅抗性。

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