miR-126在胃腺癌中通过靶血管内皮生长因子- a调控血管生成

Yupeng Lei, Hongxia Chen, F. Shi, Xiaodong Zhou
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引用次数: 1

摘要

miR-126是一种内皮特异性microRNA,对控制血管完整性和血管生成至关重要。其在胃癌血管生成中的作用尚不清楚。本研究旨在确定miR-126在GC血管生成中的作用。研究发现,miR-126的下调与胃癌组织中微血管密度(MVD)和血管内皮生长因子A (VEGF-A)表达的增加呈负相关。生物信息学分析和荧光素酶报告基因检测显示,miR-126直接靶向VEGF-A mRNA的3'-非翻译区(3'-UTR)。此外,通过慢病毒-miR-126 (lentii -miR-126)转染恢复miR-126表达后,胃癌细胞系SGC-7901、MKN-28和MKN-45中VEGF-A的表达及其下游基因Akt、mTOR和Erk1/2的活性明显降低。相反,慢病毒-抗miR-126 (lentii -anti-miR-126)转染下调miR-126表达后,VEGF-A及其下游信号通路的表达明显上调。异种移植小鼠体内模型实验阐明了上调miR-126下调VEGF-A和MVD,抑制肿瘤生长的作用。综上所述,我们的研究结果表明miR-126可以通过VEGF-A信号抑制胃癌的肿瘤生长和肿瘤血管生成,是胃癌新的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miR-126 regulates angiogenesis by target vascular endothelial growth factor-A in gastric adenocarcinoma
miR-126 is an endothelial-specific microRNA essential for governing vascular integrity and angiogenesis. Its role in tumor angiogenesis of gastric cancer (GC) is unclear. This study aimed at determining the role of miR-126 in GC angiogenesis.  Down-regulation of miR-126 was found to inversely correlate with an increased microvessel density (MVD) and vascular endothelial growth factor A (VEGF-A) expression in gastric cancer tissues. Bioinformatics analysis and luciferase reporter assay revealed that miR-126 directly targeted the 3'-untranslated region (3'-UTR) of VEGF-A mRNA. In addition, the restoration of miR-126 expression by lentivirus-miR-126 (Lenti-miR-126) transfection obviously reduced the expression of VEGF-A and the activition of its downstream genes, Akt, mTOR and Erk1/2 in gastric cancer cell lines SGC-7901, MKN-28 and MKN-45. In contrast, the down-regulation of miR-126 expression by lentivirus-anti-miR-126 (Lenti-anti-miR-126) transfection obviously up-regulated the expression of VEGF-A and its downstream signaling pathways. In vivo xenograft mice model experiments clarified the down-regulation of VEGF-A and MVD as well as inhibition of tumor growth by up-regulation of miR-126. Overall, the results from our study suggested that miR-126 could suppress tumor growth and tumor angiogenesis of GC through VEGF-A signaling, and it is a novel potential therapeutic target for GC.
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