Abstract | OBJECTIVE: METHODS: HepG2 cells were administrated with simvastatin. Proliferation of the cells was detected by MTT assay, cell cycle was measured by flowcytometry and the cyclin-dependent kinase inhibitor p21 protein expression was detected by immunocytochemistry. The results were evaluated by factorial design and one-way analysis of variance. RESULTS:
Simvastatin inhibited HepG2 cells growth in vitro (F(concentration) = 1264, P value less than 0.001; F(time) = 17.466, P value less than 0.001; F(concentration*time) = 35.053, P value less than 0.001) and could arrest HepG2 cells in G0/G1 phase of cell cycle. However, apoptosis of HepG2 cells was not obvious. Simvastatin could also increase cyclin-dependent kinase inhibitor p21 protein expression (F = 512.133, P value less than 0.001). CONCLUSION:
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Authors | Wei Liu, Lian-feng Zhang, Yu-heng Zhang |
Journal | Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology
(Zhonghua Gan Zang Bing Za Zhi)
Vol. 18
Issue 10
Pg. 751-3
(Oct 2010)
ISSN: 1007-3418 [Print] China |
PMID | 21059291
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- CDKN1A protein, human
- Cyclin-Dependent Kinase Inhibitor p21
- Simvastatin
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Topics |
- Carcinoma, Hepatocellular
(metabolism, pathology)
- Cell Cycle
(drug effects)
- Cell Proliferation
(drug effects)
- Cyclin-Dependent Kinase Inhibitor p21
(metabolism)
- Hep G2 Cells
- Humans
- Liver Neoplasms
(metabolism, pathology)
- Simvastatin
(pharmacology)
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