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1.
Acta Academiae Medicinae Sinicae ; (6): 661-665, 2004.
Article in Chinese | WPRIM | ID: wpr-343787

ABSTRACT

<p><b>OBJECTIVE</b>To establish a protocol for the targeting gene therapy against cancer with rich epidermal growth factor receptor (EGFR).</p><p><b>METHODS</b>A recombinant pcDNA3.1-PE III mut was constructed and combined with a non-viral vector, a fusion protein histone H1, epidermal growth factor C-loop previously expressed by us, to be a protein-DNA complex in vitro. Using the complex to treat BT-325 and Hela cancer cells with EGFR and JK cells without EGFR. The killing rates of the cells was calculated after 48 h of incubation at 37 degrees C.</p><p><b>RESULTS</b>To BT-325 and Hela cells, the killing rates were 46.03% and 48.12% respectively. To JK cells, the complex had no killing function.</p><p><b>CONCLUSION</b>The protocol for targeting gene therapy against cancer with EGFR has been established successfully.</p>


Subject(s)
Humans , ADP Ribose Transferases , Genetics , Pharmacology , Bacterial Toxins , Genetics , Pharmacology , Base Sequence , Cell Line, Tumor , Cells , DNA , Genetics , Exotoxins , Genetics , Pharmacology , Gene Targeting , Genetic Therapy , Genetic Vectors , Histones , Genetics , Molecular Sequence Data , ErbB Receptors , Genetics , Metabolism , Recombinant Fusion Proteins , Genetics , Metabolism , Pharmacology , Transfection , Virulence Factors , Genetics , Pharmacology
2.
Acta Academiae Medicinae Sinicae ; (6): 381-384, 2002.
Article in Chinese | WPRIM | ID: wpr-278159

ABSTRACT

<p><b>OBJECTIVE</b>To create a gene transfer vehicle for targeting gene therapy of cancer with epidermal growth factor receptor overexpressing.</p><p><b>METHODS</b>Encoding sequences of the first domain of histone gene (H1) and EGF C-loop (EGFc) were obtained by PCR amplification. These two DNA fragments were ligated by EcoR I site, and cloned and sequenced. E. coli expression vector of the fusion gene was then constructed. The fusion protein H1EGFc was purified by specific band isolation from SDS-PAGE.</p><p><b>RESULTS</b>The molecular weight of purified protein was consistent with the designed request. Its purity reached 94.02%.</p><p><b>CONCLUSION</b>A fusion protein H1EGFc was expressed and purified.</p>


Subject(s)
Humans , Amino Acid Sequence , Base Sequence , Escherichia coli , Genetics , Gene Transfer Techniques , Genetic Therapy , Genetic Vectors , Histones , Genetics , Molecular Sequence Data , Protein Engineering , ErbB Receptors , Genetics , Recombinant Fusion Proteins , Genetics
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