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上皮膜蛋白1真核表达载体的构建及其对人舌鳞状癌细胞迁移和侵袭的影响

[Construction of epithelial membrane protein 1 eukaryotic expression vector and its influence on migration and invasion of human oral tongue squamous carcinoma cells].

作者信息

Xiaohua Dai, Jun Zhang, Huiru Zou, Xiaoli Lian, Yanni Li, Guanhua Wang, Yan Yan

机构信息

Research Center, Tianjin Stomatological Hospital, Stomatological Hospital of Nankai University, Tianjin 300041, China.

Dept. of Oral and Maxillofacial Surgery, Tianjin Stomatological Hospital, Stomatological Hospital of Nankai University, Tianjin 300041, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2016 Aug 1;34(4):398-403. doi: 10.7518/hxkq.2016.04.016.

Abstract

OBJECTIVE

This study aimed to construct a eukaryotic expression vector pEGFP-N1-EMP1 of epithelial mem-brane protein 1 (EMP1) and investigate its influence on migration and invasion of human oral tongue squamous carcinoma cells.

METHODS

The human EMP1 gene was amplified by reverse transcription polymerase chain reaction and then ligated into the pEGFP-N1 vector by double restriction endonuclease digestion to construct pEGFP-N1-EMP1 recombinant plasmid. After sequencing identification, pEGFP-N1-EMP1 recombinant plasmid and pEGFP-N1 plasmid were transfected into human oral tongue squamous carcinoma Tb3.1 cell line. The expression of green fluorescent protein in cells was observed after transfection using an inverted fluorescence microscope. The overexpression of EMP1 mRNA was identified at 24, 48, and 72 h after transfection by real-time fluorescence quantitative polymerase chain reaction. The effect of EMP1 overexpression on migration and invasion of Tb3.1 cells was detected by Transwell assay.

RESULTS

The full-length EMP1 gene sequence was successfully obtained. Sequence analysis showed that the EMP1 gene was inserted into the pEGFP-N1 vector correctly. Green fluorescence was observed in the transfected cells under fluorescence microscopy. The results of real-time fluorescence quantitative polymerase chain reaction indicated that the expression of EMP1 at 24 h after pEGFP-N1-EMP1 transfection was significantly higher than the other groups. Transwell assays indicated that overexpression of the EMP1 gene could significantly inhibit the migration and invasion ability of Tb3.1 cells.

CONCLUSIONS: The eukaryotic expression vector of EMP1 was successfully constructed, and EMP1 overexpression was confirmed to inhibit the migration and inva-sion of oral tongue squamous carcinoma cells in vitro. This study laid a foundation for further investigation on the influence of the EMP1 gene on the metastasis of oral tongue squamous carcinoma and its molecular mechanism.
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摘要

目的

构建上皮膜蛋白1(EMP1)的真核表达载体pEGFP-N1-EMP1,并研究其对人舌鳞状癌细胞迁移和侵袭能力的影响。

方法

通过逆转录聚合酶链反应扩增人EMP1基因,然后经双酶切连接至pEGFP-N1载体,构建pEGFP-N1-EMP1重组质粒。测序鉴定后,将pEGFP-N1-EMP1重组质粒和pEGFP-N1质粒转染至人舌鳞状癌Tb3.1细胞系。转染后利用倒置荧光显微镜观察细胞中绿色荧光蛋白的表达情况。采用实时荧光定量聚合酶链反应在转染后24、48和72小时鉴定EMP1 mRNA的过表达情况。通过Transwell实验检测EMP1过表达对Tb3.1细胞迁移和侵袭能力的影响。

结果

成功获得EMP1基因全长序列。序列分析表明EMP1基因正确插入pEGFP-N1载体。荧光显微镜下观察到转染细胞中有绿色荧光。实时荧光定量聚合酶链反应结果显示,pEGFP-N1-EMP1转染后24小时EMP1的表达显著高于其他组。Transwell实验表明,EMP1基因过表达可显著抑制Tb3.1细胞的迁移和侵袭能力。

结论

成功构建了EMP1真核表达载体,证实EMP1过表达在体外可抑制舌鳞状癌细胞的迁移和侵袭。本研究为进一步探讨EMP1基因对舌鳞状癌转移的影响及其分子机制奠定了基础。

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