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The role of microRNA-21 in predicting brain metastases from non-small cell lung cancer

机译:microRNA-21在预测非小细胞肺癌脑转移中的作用

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摘要

Objective: This study aimed at exploring the role of microRNA-21 (miR-21) in predicting brain metastases (BM) from non-small cell lung cancer (NSCLC). Methods: A total of 132 NSCLC patients, including 68 patients with BM and 64 patients without BM, were included in the study. NSCLC cells were collected and assigned to the inhibitor (IN) group, the mock group, and the negative control (NC) group. The quantitative real-time polymerase chain reaction assay was used to detect the miR-21 expression. Cell proliferation, migration, invasion, and apoptosis were detected by colony-forming assay, MTT assay, transwell assay, and flow cytometry, respectively. Angiogenesis was measured by endothelial cell tube formation assay. Results: The miR-21 expression was higher in NSCLC patients with BM than in those without BM. The miR-21 expression in the IN group was lower than that in the NC and mock groups. Compared with the NC and mock groups, the values of optical density (OD) and the colony-forming number decreased in the IN group. Compared with the NC and mock groups, cell invasion and migration abilities significantly reduced in the IN group. The IN group had higher apoptosis rate than the NC and mock groups. The tube length was shorter and the number of junction points was less in the IN group in comparison to the NC and mock groups. Conclusion: miR-21 might be a potential biomarker for the development of BM in NSCLC patients and could promote the proliferation, migration, invasion, and angiogenesis of NSCLC cells.
机译:目的:本研究旨在探讨microRNA-21(miR-21)在预测非小细胞肺癌(NSCLC)脑转移(BM)中的作用。方法:本研究共纳入132例NSCLC患者,包括68例BM患者和64例非BM患者。收集NSCLC细胞,并分配给抑制剂(IN)组,模拟组和阴性对照(NC)组。使用定量实时聚合酶链反应测定法检测miR-21表达。通过集落形成测定,MTT测定,transwell测定和流式细胞术分别检测细胞增殖,迁移,侵袭和凋亡。通过内皮细胞管形成测定法测量血管生成。结果:BM的NSCLC患者的miR-21表达高于无BM的患者。 IN组的miR-21表达低于NC组和模拟组。与NC组和模拟组相比,IN组的光密度(OD)值和菌落形成数降低。与NC组和模拟组相比,IN组的细胞侵袭和迁移能力显着降低。 IN组的凋亡率高于NC组和模拟组。与NC组和模拟组相比,IN组的管长更短且连接点的数量更少。结论:miR-21可能是NSCLC患者BM发展的潜在生物标志物,并可能促进NSCLC细胞的增殖,迁移,侵袭和血管生成。

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