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Expression and role of VEGFA and miR-381 in portal vein tumor thrombi in patients with hepatocellular carcinoma

机译:肝细胞癌患者门静脉肿瘤血栓中VEGFA和miR-381的表达及其作用

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摘要

The aim of the present study was to examine the expression and role of vascular endothelial growth factor A (VEGFA) and microRNA (miRNA or miR)-381 in tumor thrombi from patients with hepatocellular carcinoma and portal vein tumor thrombus (PVTT). Tumor thrombi and adjacent paired tissues were collected from 39 patients with hepatocellular carcinoma with PVTT. VEGFA expression levels were assessed using reverse transcription-quantitative polymerase chain reaction and western blotting. miRNAs that may regulate VEGFA expression were predicted using bioinformatics analysis and confirmed via a dual luciferase reporter assay. The effects of VEGFA and its upstream miRNA on proliferation of the proliferation of EAhy926 human venous endothelial cells were analyzed using an MTT assay. Compared with the paired adjacent tissues, VEGFA was significantly upregulated at both the mRNA and protein level in tumor thrombi (P<0.05). VEGFA was predicted to be a target of miR-381 and this was confirmed experimentally. miR-381 expression was significantly downregulated in tumor thrombi from patients with PVTT compared with paired adjacent tissues (P<0.05). In addition, transfection with antagomirs against miR-381 or short interfering RNA against VEGFA significantly inhibited EAhy926 cell proliferation (P<0.05). In conclusion, the results of the present study indicate that VEGFA is upregulated in tumor thrombi whereas miR-381 is downregulated. VEGFA is regulated by miR-381 and both may be associated with the development of PVTT.
机译:本研究的目的是检查肝细胞癌和门静脉肿瘤血栓(PVTT)患者的肿瘤血栓中血管内皮生长因子A(VEGFA)和microRNA(miRNA或miR)-381的表达和作用。从39例PVTT肝细胞癌患者中收集肿瘤血栓和邻近的配对组织。使用逆转录定量聚合酶链反应和蛋白质印迹法评估VEGFA的表达水平。使用生物信息学分析预测可能调节VEGFA表达的miRNA,并通过双重萤光素酶报告基因测定法确认。使用MTT分析法分析了VEGFA及其上游miRNA对EAhy926人静脉内皮细胞增殖的影响。与配对的相邻组织相比,VEGFA在肿瘤血栓中的mRNA和蛋白水平均显着上调(P <0.05)。 VEGFA被预测为miR-381的靶标,并且实验证实了这一点。与配对的相邻组织相比,PVTT患者的肿瘤血栓中的miR-381表达显着下调(P <0.05)。此外,转染抗miR-381的拟南芥或抗VEGFA的短干扰RNA均能显着抑制EAhy926细胞的增殖(P <0.05)。总之,本研究的结果表明,VEGFA在肿瘤血栓中被上调,而miR-381被下调。 VEGFA受miR-381调节,两者均可能与PVTT的发展有关。

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