Source:http://linkedlifedata.com/resource/pubmed/id/17593797
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-6-27
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pubmed:abstractText |
Our previous studies have found that reducing expression of myeloid zinc finger-1 (MZF-1) inhibited protein kinase C alpha (PKCalpha) expression and decreased cell migration and invasion in human hepatocellular carcinoma (HCC). In this study, we further investigated the role of MZF-1 in tumorigenesis. The SK-Hep-1 HCC cells were transfected with the antisense oligonucleotide (ODN) of MZF-1. The pretreated cells was then detected the mRNA and protein levels by RT-PCR and western blotting, and the cell growth was assayed by MTT. Meanwhile, the pretreated-SK-Hep-1 HCC cells were implanted subcutaneously into nude mice to observe the tumor growth and calculated tumor inhibitory rate. The results showed that, at the dosage of 5 microM, the antisense ODN MZF-1 suppressed both MZF-1 and PKCalpha productions by SK-Hep-1 HCC cells after cationic liposome-mediated transfection, to 15% and 30% in control cultures of 0 microM dosage, respectively. The growth of SK-Hep-1 HCC cells was inhibited by the 2-5 microM doses of the antisense ODN MZF-1, whereas the control reagent, the sense ODN MZF-1, showed no effects. In BALB/nude mice, SK-Hep-1 HCC cells pretreated with the 5 microM antisense ODN MZF-1 formed tumors much smaller than the cells with sense ODN. The mean of inhibitory rate of tumor growth was 71.2 +/- 8.6%, and the tumor formation time was prolonged from 14 days to 26 days. These findings suggested the usefulness of antisense ODN MZF-1 as a new reagent for cancer therapy.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0304-4920
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
9-15
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pubmed:dateRevised |
2009-8-12
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pubmed:meshHeading |
pubmed-meshheading:17593797-Animals,
pubmed-meshheading:17593797-Carcinogenicity Tests,
pubmed-meshheading:17593797-Carcinoma, Hepatocellular,
pubmed-meshheading:17593797-Cell Division,
pubmed-meshheading:17593797-Cell Line, Tumor,
pubmed-meshheading:17593797-Dose-Response Relationship, Drug,
pubmed-meshheading:17593797-Humans,
pubmed-meshheading:17593797-Kruppel-Like Transcription Factors,
pubmed-meshheading:17593797-Liver Neoplasms,
pubmed-meshheading:17593797-Mice,
pubmed-meshheading:17593797-Mice, Inbred BALB C,
pubmed-meshheading:17593797-Mice, Nude,
pubmed-meshheading:17593797-Neoplasm Transplantation,
pubmed-meshheading:17593797-Oligonucleotides, Antisense,
pubmed-meshheading:17593797-Transfection
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pubmed:year |
2007
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pubmed:articleTitle |
Suppression of tumorigenicity of human hepatocellular carcinoma cells by antisense oligonucleotide MZF-1.
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pubmed:affiliation |
Institute of Biochemistry and Biotechnology, Chung-Shan Medical University, Taichung, Taiwan, ROC.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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