首页> 美国卫生研究院文献>Oncology Letters >miR-339-5p inhibits cell migration and invasion in vitro and may be associated with the tumor-node-metastasis staging and lymph node metastasis of non-small cell lung cancer
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miR-339-5p inhibits cell migration and invasion in vitro and may be associated with the tumor-node-metastasis staging and lymph node metastasis of non-small cell lung cancer

机译:miR-339-5p在体外抑制细胞迁移和侵袭可能与非小细胞肺癌的肿瘤淋巴结转移和淋巴结转移有关

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摘要

The aim of the present study was to investigate the potential role of microRNA (miRNA or miR) in invasion and metastasis of non-small cell lung cancer (NSCLC). miRNA-microarray analysis was used to detect the differentially expressed miRNAs between various metastatic levels of NSCLC cells. The microarray results were verified by quantitative polymerase chain reaction. The most clearly altered miRNA, miR-339-5p, was transfected into NSCLC cells and cell migration and invasion were investigated. The expression of miR-339-5p was 3.4662-fold higher in the lower metastatic NSCLC cells. miR-339-5p significantly decreased tumor-cell migration and the invasion capacity in vitro. In conclusion, miR-339-5p is important in NSCLC invasion and metastasis, indicating that miR-339-5p could be further evaluated as a biomarker for predicting the survival time of patients with NSCLC.
机译:本研究的目的是研究microRNA(miRNA或miR)在非小细胞肺癌(NSCLC)侵袭和转移中的潜在作用。 miRNA-微阵列分析用于检测NSCLC细胞各种转移水平之间差异表达的miRNA。通过定量聚合酶链反应验证了微阵列结果。将改变最明显的miRNA miR-339-5p转染到NSCLC细胞中,并对细胞迁移和侵袭进行了研究。在较低转移性NSCLC细胞中,miR-339-5p的表达高3.4662倍。 miR-339-5p显着降低了肿瘤细胞的迁移和体外侵袭能力。总之,miR-339-5p在NSCLC的侵袭和转移中很重要,表明miR-339-5p可以被进一步评估为预测NSCLC患者生存时间的生物标志物。

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