Abstract | BACKGROUND: METHODS: Cell growth and viability were evaluated by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay. The in vivo efficacy of vitamin K(2) was examined in nude mice bearing HCC cells. A 24-well transwell chamber was used to evaluate the motility and invasive ability of HCC cells. Levels of DCP in supernatant of cultures and in serum of mice were measured using an electrochemiluminescence immunoassay method. Western blot and immunohistochemical analysis were employed to evaluate the expression of DCP in HCC. RESULTS:
Vitamin K(2) (2-40 muM) significantly decreased the levels of DCP production in supernatant of PLC/PRF/5 and HepG2 cells and in serum of nude mice bearing HCC xenografts. The inhibition of DCP was also observed using the assays of Western blot analysis in HCC cultures and immunohistochemical analysis in HCC xenografts in mice. As a result of administration of vitamin K(2), the capacity of HCC growth was inhibited and the invasion and migration of tumor cells were decreased. Furthermore, the inhibitory effects of HCC growth were also observed in vivo and the sensitivity was well correlated with the decrease of DCP in the serum of mice. CONCLUSION:
Vitamin K(2) might suppress the growth and invasion of HCC cells via decrease of DCP.
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Authors | Meng Ma, Xian-Jun Qu, Guo-Ying Mu, Ming-Hui Chen, Yan-Na Cheng, Norihiro Kokudo, Wei Tang, Shu-Xiang Cui |
Journal | Chemotherapy
(Chemotherapy)
Vol. 55
Issue 1
Pg. 28-35
( 2009)
ISSN: 1421-9794 [Electronic] Switzerland |
PMID | 18974646
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | (c) 2008 S. Karger AG, Basel. |
Chemical References |
- Biomarkers
- Protein Precursors
- Vitamin K 2
- acarboxyprothrombin
- Prothrombin
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Topics |
- Animals
- Biomarkers
(metabolism)
- Blotting, Western
- Carcinoma, Hepatocellular
(metabolism, pathology)
- Cell Division
(drug effects)
- Cell Line, Tumor
- Humans
- Liver Neoplasms
(metabolism, pathology)
- Luminescent Measurements
- Mice
- Mice, Nude
- Neoplasm Invasiveness
- Protein Precursors
(drug effects, metabolism)
- Prothrombin
(drug effects, metabolism)
- Vitamin K 2
(metabolism, pharmacology)
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