Effects of over-expression of MAGE-A3 on human hepatocellular carcinoma cell line SMMC7721
Zhong Chen, Jinbing Sun
Abstract
Zhong Chen, Jinbing Sun
Abstract
Objective To observe the effects of over-expression of target gene MAGE-A3 by transient transfection on proliferation and metastasis of human hepatocellular carcinoma (HCC) cell lines.Methods MAGE-A3 target gene that containing restriction enzyme cutting site of NheI and KpnI was obtained by reverse transcription-polymerase chain reaction (RT-PCR) from HCC tissues.The target gene was cloned into the expression vector pcDNA3.1 ( - ) to construct MAGE-A3 eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3,which was checked by restrictive enzyme digestion and DNA sequencing,and then transiently transfected into human HCC cell line SMMC7721 with Lipofectamine 2000.The mRNA and protein expression of MAGE-A3 was detected by semi-quantitive RT-PCR and Western blotting assay respectively.MTT assay and Boyden chamber assay were performed to detect the effects of MAGE-A3 on colony formation and metastasis.Results MAGE-A3 target gene was amplified and the eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3 was correctly constructed,and confirmed by restrictive enzyme digestion and DNA sequencing. RT-PCR and Western blotting revealed a strongly increased level of MAGE-A3 mRNA and protein expression in transfection group as compared with untransfected group and empty vector-transfected group (for MAGE-A3 mRNA expression level: 7838,2847 and 1557 in three groups,and for MAGE-A3 protein levels: 30 938,24 088 and 29 654,respectively).Both the number of HCC cells transfected by peDNA3.1-MAGE-A3 in MTT assay and the number of cells penetrating matrigel were increased as compared with untransfected group and empty vector-transfected group (P <0.05 ).Conclusion The eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3 was successfully constructed.The number of cells and invasiveness of the HCC cells transfected by pcDNA3.1-MAGE-A3 were significantly increased,suggesting MAGE-A3 gene may play a significant role in proliferation and metastasis of human HCC. Key words: MAGE; Transfect; Carcinoma,hepatocellular; Proliferation
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To observe the effects of over-expression of target gene MAGE-A3 by transient transfection on proliferation and metastasis of human hepatocellular carcinoma (HCC) cell lines.Methods MAGE-A3 target gene that containing restriction enzyme cutting site of NheI and KpnI was obtained by reverse transcription-polymerase chain reaction (RT-PCR) from HCC tissues.The target gene was cloned into the expression vector pcDNA3.1 ( - ) to construct MAGE-A3 eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3,which was checked by restrictive enzyme digestion and DNA sequencing,and then transiently transfected into human HCC cell line SMMC7721 with Lipofectamine 2000.The mRNA and protein expression of MAGE-A3 was detected by semi-quantitive RT-PCR and Western blotting assay respectively.MTT assay and Boyden chamber assay were performed to detect the effects of MAGE-A3 on colony formation and metastasis.Results MAGE-A3 target gene was amplified and the eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3 was correctly constructed,and confirmed by restrictive enzyme digestion and DNA sequencing. RT-PCR and Western blotting revealed a strongly increased level of MAGE-A3 mRNA and protein expression in transfection group as compared with untransfected group and empty vector-transfected group (for MAGE-A3 mRNA expression level: 7838,2847 and 1557 in three groups,and for MAGE-A3 protein levels: 30 938,24 088 and 29 654,respectively).Both the number of HCC cells transfected by peDNA3.1-MAGE-A3 in MTT assay and the number of cells penetrating matrigel were increased as compared with untransfected group and empty vector-transfected group (P <0.05 ).Conclusion The eukaryotic recombinant expression plasmid pcDNA3.1-MAGE-A3 was successfully constructed.The number of cells and invasiveness of the HCC cells transfected by pcDNA3.1-MAGE-A3 were significantly increased,suggesting MAGE-A3 gene may play a significant role in proliferation and metastasis of human HCC. Key words: MAGE; Transfect; Carcinoma,hepatocellular; Proliferation
Key concepts: Transfection, Lipofectamine, Molecular biology, Blot, Recombinant DNA, Cell culture, Biology, MTT assay