Abstract |
20-O-(beta-D-glucopyranosyl)-20(S)-protopanaxadiol (IH-901), a novel intestinal bacterial metabolite of ginseng protopanaxadiol saponins, is reported to induce apoptosis in a variety of cancer cells. We purified the compound and measured its in vitro anti- tumor activity. IH-901 inhibited cell growth of human hepatocellular carcinoma SMMC7721 cells in a dose- and time-dependent manner. We also found that IH-901 induced apoptotic cell death concurrent with cell cycle arrest in G0-G1 phase in SMMC7721 cells. At the molecular level, we show that IH-901 upregulates cytochrome c, p53, and Bax expression, and downregulates pro-caspase-3 and pro-caspase-9 expressions in a dose-dependent manner, while the levels of Bcl-2 and Bcl-X(L) were unchanged in IH-901-treated SMMC7721 cells. These results provide significant insight into the anticarcinogenic action of IH-901.
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Authors | Yan-lin Ming, Gang Song, Liang-hua Chen, Zhi-zhong Zheng, Zhong-yan Chen, Gao-liang Ouyang, Qing-xuan Tong |
Journal | Cell biology international
(Cell Biol Int)
Vol. 31
Issue 10
Pg. 1265-73
(Oct 2007)
ISSN: 1065-6995 [Print] England |
PMID | 17587608
(Publication Type: Journal Article)
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Chemical References |
- 20-O-(beta-D-glucopyranosyl)-20(S)-protopanaxadiol
- BAX protein, human
- Proto-Oncogene Proteins c-bcl-2
- Sapogenins
- Tumor Suppressor Protein p53
- bcl-2-Associated X Protein
- bcl-X Protein
- Cytochromes c
- Caspase 3
- Caspase 9
- Caspases
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Topics |
- Apoptosis
(drug effects)
- Blotting, Western
- Carcinoma, Hepatocellular
(drug therapy, metabolism, pathology)
- Caspase 3
(metabolism)
- Caspase 9
(metabolism)
- Caspases
(metabolism)
- Cell Proliferation
(drug effects)
- Cytochromes c
(metabolism)
- Flow Cytometry
- Humans
- Liver Neoplasms
(drug therapy, metabolism, pathology)
- Proto-Oncogene Proteins c-bcl-2
(metabolism)
- Sapogenins
(pharmacology)
- Tumor Cells, Cultured
- Tumor Suppressor Protein p53
(metabolism)
- bcl-2-Associated X Protein
(metabolism)
- bcl-X Protein
(metabolism)
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