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MicroRNA-29c functions as a tumor suppressor by targeting VEGFA in lung adenocarcinoma

机译:MicroRNA-29c通过靶向VEGFA在肺腺癌中起抑癌作用

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BackgroundLung adenocarcinoma (LAD) is considered to be a highly aggressive disease with heterogeneous prognosis and the molecular mechanisms underlying tumor progression remain elusive. Growing evidence demonstrates that the dysregulation of microRNAs (miRNAs) plays an important role in various tumor processes. The aim of this study is to discover prognostic miRNA and investigate its role involved in progression of LAD. MethodsPrognosis related miRNA was detected by miRNA microarray using formalin-fixed paraffin-embedded (FFPE) specimens from 87 patients with IIIA-N2 LAD. The cell proliferation was evaluated by Cell Titer 96 AQueous One Solution Cell Proliferation Assay (MTS), and the migration/invasion was evaluated by transwell assay. The bioinformatics methods and luciferase reporter assay were applied to detect the relationship between miRNA and its target. The mRNA and protein levels of miRNA target were determined by quantitative real time polymerase chain reaction (qRT-PCR) analysis, western blot and enzyme-linked immunosorbent assay (ELISA). Changes of angiogenesis induced by miRNA was evaluated by human umbilical vein endothelial cell (HUVEC) tube formation assay. Immunohistochemistry (IHC) analysis was performed in FFPE specimens of patients to evaluate the correlation between miR-29c with microvessel density (MVD) and?vascular endothelial growth factor A (VEGFA) expression. ResultsMiR-29c expression downregulation was significantly associated with unfavorable prognosis in IIIA-N2 LAD. MiR-29c inhibited cell proliferation, migration and invasion in cell lines. Integrated analysis revealed that VEGFA was a direct target of miR-29c. MiR-29c reduced the capability of tumor cells to promote HUVEC tube formation. The compromised cell proliferation, migration/invasion and angiogenesis induced by miR-29c mimic transfection were reversed by transfection of VEGFA expression plasmid. Furthermore, the correlation of miR-29c with MVD and VEGFA was confirmed in patients’ samples. ConclusionsMiR-29c acts as a tumor suppressor by targeting VEGFA and may represent a promising prognostic biomarker as well as a potential therapeutic target for LAD.
机译:背景肺腺癌(LAD)被认为是具有高度异质性预后的高度侵袭性疾病,而肿瘤进展的分子机制仍然难以捉摸。越来越多的证据表明,microRNA(miRNA)的失调在各种肿瘤过程中起着重要作用。这项研究的目的是发现预后的miRNA,并研究其在LAD进展中的作用。方法使用87例IIIA-N2型LAD患者的福尔马林固定石蜡包埋(FFPE)标本,通过miRNA微阵列检测预后相关的miRNA。通过Cell Titer 96 AQueous One Solution细胞增殖测定法(MTS)评估细胞增殖,并通过transwell测定法评估迁移/侵袭。应用生物信息学方法和荧光素酶报告基因检测法检测miRNA与其靶标之间的关系。通过定量实时聚合酶链反应(qRT-PCR)分析,蛋白质印迹和酶联免疫吸附测定(ELISA)确定miRNA目标的mRNA和蛋白水平。通过人脐静脉内皮细胞(HUVEC)管形成分析评估了miRNA诱导的血管生成的变化。对患者的FFPE标本进行了免疫组织化学(IHC)分析,以评估miR-29c与微血管密度(MVD)和血管内皮生长因子A(VEGFA)表达之间的相关性。结果MiR-29c表达下调与IIIA-N2 LAD预后不良有关。 MiR-29c抑制细胞系中的细胞增殖,迁移和侵袭。综合分析表明,VEGFA是miR-29c的直接靶标。 MiR-29c降低了肿瘤细胞促进HUVEC管形成的能力。通过转染VEGFA表达质粒可逆转miR-29c模拟转染诱导的受损细胞增殖,迁移/侵袭和血管生成。此外,在患者样本中证实了miR-29c与MVD和VEGFA的相关性。结论MiR-29c通过靶向VEGFA发挥抑癌作用,可能代表有希望的预后生物标志物以及LAD的潜在治疗靶标。

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