Abstract | BACKGROUND AND AIMS: METHODS: 7721-IGF-IR-AS cells (human hepatoma SMMC-7721 cells transfected with IGF-IR antisense gene in our previous study) were transfected with a plasmid vector expressing IGF-IIR cDNA in the antisense orientation by DOTAP liposome.7721-IGF-R-AS cells were obtained by selection with G418 and hygromycin. Morphological changes of the cells were observed with optic and electron microscopes. In vitro growth of the 7721-IGF-R-AS cells was observed with a soft agar test, MTT test and with naked mice inoculation test in vivo. RESULTS: The following changes were found in the SMMC-7721 cells after being transfected with the IGF-IR and IGF-IIR antisense genes: (i) the degree of malignancy of the tumor cells as revealed by cell morphology was ameliorated; (ii) the growth capability of the tumor cells in soft agar and their tumorigenicity in naked mice were significantly depressed. However, in the control groups, the SMMC-7721 cells transfected both with IGF-IR and IGF-IIR sense cDNA and SMMC-7721 cells transfected without any external genes, had no such changes. However, the cell growth curves had no significant differences among these three groups. CONCLUSION: IGF-IR and IGF-IIR antisense genes could significantly restrain the malignant behavior of human hepatoma cells and might be useful in investigating a potential route for hepatocellular carcinoma gene therapy.
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Authors | Jian-Min Yang, Wen-Sheng Chen, Zhi-Peng Liu, Yuan-Hui Luo, Wei-Wen Liu |
Journal | Journal of gastroenterology and hepatology
(J Gastroenterol Hepatol)
Vol. 18
Issue 3
Pg. 296-301
(Mar 2003)
ISSN: 0815-9319 [Print] Australia |
PMID | 12603530
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Biomarkers, Tumor
- DNA, Antisense
- DNA, Neoplasm
- Receptor, IGF Type 2
- Receptors, Somatomedin
- Receptor, IGF Type 1
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Topics |
- Animals
- Biomarkers, Tumor
(genetics, metabolism)
- Carcinogenicity Tests
- Carcinoma, Hepatocellular
(genetics)
- Cell Division
(physiology)
- Cell Nucleus
(ultrastructure)
- China
- Cytoplasm
(ultrastructure)
- DNA, Antisense
(chemistry, genetics, metabolism)
- DNA, Neoplasm
(genetics)
- Humans
- Liver
(cytology)
- Liver Neoplasms
(genetics)
- Mice
- Microscopy, Electron, Scanning
- Receptor, IGF Type 1
(genetics, metabolism)
- Receptor, IGF Type 2
(genetics, metabolism)
- Receptors, Somatomedin
(genetics, metabolism)
- Transfection
- Tumor Cells, Cultured
(cytology, metabolism)
- Tumor Stem Cell Assay
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