首页> 外文期刊>Journal of International Medical Research >Serum microRNA-365 suppresses non-small-cell lung cancer metastasis and invasion in patients with bone metastasis of lung cancer
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Serum microRNA-365 suppresses non-small-cell lung cancer metastasis and invasion in patients with bone metastasis of lung cancer

机译:血清MicroRNA-365抑制肺癌骨转移患者的非小细胞肺癌转移和侵袭

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Objective In the present investigation, we evaluated the effects of microRNA-365 (miR-365) on non-small-cell lung cancer (NSCLC) cell metastasis and invasion in patients with bone metastasis of lung cancer. Methods Blood samples from patients with NSCLC and healthy controls and the A549 adenocarcinoma cell line were included in this study. Quantitative real-time PCR and microarray were performed on blood samples. The MTT assay, luciferase reporter assay, Transwell assay, ELISA, and western blot were performed to evaluate expression of associated factors. Results Expression of miR-365 was reduced in patients with bone metastasis of NSCLC. Downregulation of miR-365 promoted cell growth, metastasis, and invasion of NSCLC. Upregulation of miR-365 reduced cell growth, metastasis, and invasion of NSCLC. Downregulation of miR-365 induced expression of NKX homeobox-1 (NKX2-1), epidermal growth factor receptor (EGFR), phosphoinositide-3-kinase (PI3K), and p-Akt proteins in an in vitro model of NSCLC. Inhibition of NKX2-1 reduced the effects of miR-365 on cell growth, metastasis, and invasion of NSCLC. Activation of EGFR reduced the effects of miR-365 on cell growth, metastasis, and invasion of NSCLC. Conclusions The study established that the serum miR-365 suppresses NSCLC cell metastasis and invasion in patients with bone metastasis of lung cancer via EGFR/PI3K through NKX2-1.
机译:目的在本发明的调查中,我们评估了MicroRNA-365(miR-365)对肺癌骨转移患者非小细胞肺癌(NSCLC)细胞转移和侵袭的影响。方法本研究还包括来自NSCLC和健康对照患者的血液样本和A549腺癌细胞系。对血液样品进行定量实时PCR和微阵列。进行MTT测定,荧光素酶报告分析,Transwell测定,ELISA和Western印迹,以评估相关因素的表达。 NSCLC骨转移患者减少了miR-365的表达。 miR-365的下调促进了NSCLC的细胞生长,转移和侵袭。 MiR-365的上调降低细胞生长,转移和侵袭NSCLC。 MiR-365的下调诱导NKX Homeobox-1(NKX2-1),表皮生长因子受体(EGFR),磷酸膦酸钠-3-激酶(PI3K)和P-AKT蛋白在NSCLC的体外模型中的表达。 NKX2-1的抑制减少了miR-365对NSCLC细胞生长,转移和侵袭的影响。 EGFR的激活降低了miR-365对NSCLC细胞生长,转移和侵袭的影响。结论该研究确定,血清MIR-365通过EGFR / PI3K通过NKX2-1抑制肺癌骨转移患者的NSCLC细胞转移和侵袭。

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