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Anti-tumor effect of recombinant retroviral vector-mediated human ANGPTL4 gene transfection

李克强 李文林 彭淑牖 石小玉 唐洪林 刘颖斌

中华医学杂志(英文版)Issue(9):1364-1369,6.
中华医学杂志(英文版)Issue(9):1364-1369,6.

Anti-tumor effect of recombinant retroviral vector-mediated human ANGPTL4 gene transfection

Anti-tumor effect of recombinant retroviral vector-mediated human ANGPTL4 gene transfection

李克强 1李文林 2彭淑牖 1石小玉 3唐洪林 2刘颖斌1

作者信息

  • 1. Department of General Surgery, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, China
  • 2. Jiangxi Key Laboratory of Medical Biotechnology, Jiangxi Medical Science Institute, Nanchang 330006, China
  • 3. Basic Medical Department of Jiangxi Medical college, Nanchang 330006, China
  • 折叠

摘要

Abstract

Background This study was designed to obtain a recombinant retroviral vector containing the human hepatocellular carcinoma-related gene ANGPTL4 (angiopoietin-like 4) cDNA and to evaluate the anti-tumor effect of recombinant retroviral vector-mediated human ANGPTL4 gene transfection.Methods ANGPTL4 cDNA was cloned in vitro from normal human liver cells HL-7702 by using RT-PCR, and then subcloned into the plasmid vector pMSCV and sequenced. The retroviral plasmid vectors pMSCV-ANGPTL4, pVSV, and pGAG-POL were co-transfected into the packaging cell line 293 EBNA under mediation of lipofectamine. A high-titer retrovirus was obtained as a result, and HepG2 cells were infected with this retrovirus in vitro. Flow cytometry and fluorescence microscopy were used to detect expression of green fluorescence protein (GFP). The expression of ANGPTL4 mRNA in HepG2-ANGPTL4 cells was investigated using RT-PCR. The formation of tumors in nude mice and MTT assays were used to detect the growth of HepG2-ANGPTL4 cells in vivo and in vitro, respectively.Results The cDNA sequence of the cloned ANGPTL4 gene was consistent with the recently reported sequence. Thus, the recombinant retroviral vector pMSCV-ANGPTL4 was constructed successfully. The titer of the packaged recombinant retrovirus was 1.4×106 infective viral grains/ml, and the rate of HepG2-ANGPTL4 cells expressing GFP was 68.45%, with an average intensity of fluorescence 31.67 times greater in HepG2-ANGPTL4 cells than in HepG2 cells. The expression of ANGPTL4 mRNA in HepG2-ANGPTL4 cells was higher than in HepG2-pMSCV cells (154% higher) or HepG2 cells (161% higher). The proliferation rate of HepG2-ANGPTL4 cells in vitro was obviously lower than those of HepG2-pMSCV cells and HepG2 cells (P<0.01). The mean volume and weight of tumors seeded from HepG2-ANGPTL4 cells were obviously lower than the mean volume or weight of tumors seeded from HepG2 cells and HepG2-pMSCV cells (P<0.01).Conclusion A stable ANGPTL4-transfected human liver cancer cell line HepG2-ANGPTL4 has been created. The transfer of the human ANGPTL4 gene mediated by a retroviral vector is a possibly effective approach for liver cancer therapy.

关键词

angiopoietin-like 4/HepG2 cell/retroviral vector

Key words

angiopoietin-like 4/HepG2 cell/retroviral vector

分类

医药卫生

引用本文复制引用

李克强,李文林,彭淑牖,石小玉,唐洪林,刘颖斌..Anti-tumor effect of recombinant retroviral vector-mediated human ANGPTL4 gene transfection[J].中华医学杂志(英文版),2004,(9):1364-1369,6.

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