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携带VEGF165-EGFP融合基因的慢病毒表达载体在乳腺癌MCF-7细胞中的构建与表达

Construction and expression of a lentivirus expression vector carrying the VEGF165-EGFP fusion gene in breast cancer MCF-7 cells.

作者信息

Luo Minna, Huang Huan, Hou Lei, Shao Shan, Huang Shangke, Zhao Xinhan

机构信息

Department of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.

Department of Radiology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, P.R. China.

出版信息

Oncol Lett. 2017 Mar;13(3):1745-1752. doi: 10.3892/ol.2017.5601. Epub 2017 Jan 17.

Abstract

Vascular endothelial growth factor (VEGF)165 is one of the most abundant and potent angiogenic factors in both physiological and pathological conditions. However, the function and mechanism of VEGF165 in tumors and their environment remain to be elucidated. In the present study, a lentivirus vector (LV) that contained the VEGF165-enhanced green fluorescent protein (EGFP) fusion gene was constructed and transfected into the human breast cancer cell line MCF-7. Following transfection, the expression of VEGF165 in MCF-7 cells was detected by reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and western blotting. Further cellular localization of VEGF165 was observed through fluorescence microscopy. The titer of the recombinant lentivirus was 5.44×10 TU/ml in the LV-VEGF165-EGFP group and 5.00×10 TU/ml in the LV-EGFP negative control group. RT-qPCR and western blotting demonstrated that the expression of VEGF165 was significantly increased in the LV-VEGF165-EGFP group compared with the control group. The present study lays the foundation for and studies on tumor cell derived-VEGF165. Furthermore, the present fusion gene expression vector may provide a potential approach for gene therapy treatment of cancer and other diseases that require regulation of angiogenesis.

摘要

血管内皮生长因子(VEGF)165是生理和病理条件下最丰富、最有效的血管生成因子之一。然而,VEGF165在肿瘤及其环境中的功能和机制仍有待阐明。在本研究中,构建了一种包含VEGF165增强绿色荧光蛋白(EGFP)融合基因的慢病毒载体(LV),并将其转染到人乳腺癌细胞系MCF-7中。转染后,通过逆转录定量聚合酶链反应(RT-qPCR)和蛋白质印迹法检测MCF-7细胞中VEGF165的表达。通过荧光显微镜观察VEGF165的进一步细胞定位。LV-VEGF165-EGFP组重组慢病毒滴度为5.44×10 TU/ml,LV-EGFP阴性对照组为5.00×10 TU/ml。RT-qPCR和蛋白质印迹法表明,与对照组相比,LV-VEGF165-EGFP组中VEGF165的表达显著增加。本研究为肿瘤细胞源性VEGF165的研究奠定了基础。此外,本融合基因表达载体可能为癌症和其他需要调节血管生成的疾病的基因治疗提供一种潜在的方法。

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