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Conference Paper: A garlic derivative S-allylcysteine suppresses liver tumor growth and metastasis by sensitizing chemotherapy
Title | A garlic derivative S-allylcysteine suppresses liver tumor growth and metastasis by sensitizing chemotherapy |
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Authors | |
Issue Date | 2008 |
Publisher | Springer New York LLC. The Journal's web site is located at http://www.springer.com/west/home/medicine?SGWID=4-10054-70-173733513-0 |
Citation | The 4th Hong Kong-Shanghai International Liver Congress (ILC 2008), Hong Kong, 12–15 June 2008. In Hepatology International, 2008, v. 2 suppl. 2, p. S105 How to Cite? |
Abstract | Background and Objective: A garlic derivative S-allylcysteine (SAC)
has anti-cancer effect in human prostate and colon cancers. We aimed
to investigate the effect of SAC and combination of chemo-drug on
tumorigenesis and metastasis of liver cancer. Materials and Methods: The orthotopic liver tumor model using a
metastatic liver cancer cell line MHCC97L labeled with luciferase gene
was applied. SAC was given at day 7 after tumor implantation at
1mg/g/day, 2mg/g/day, or 1mg/g/day combined with low dose
Cisplatin for 5 weeks. Tumor growth and metastasis were monitored by
Xenogen in vivo imaging system. Hepatic stellate cell (HSC) activation
and tumor-associated macrophage (TAM) in the tumor tissue were
detected by D-SMA and ED1/ED2 staining. Tumor micro-vessel
density (MVD) and apoptosis were also analyzed. In vitro functional
tests including MTT assay, colony formation assay, cell cycle analysis
and apoptosis analysis were performed.
Results: The tumor growth was significantly inhibited by SAC
combined with Cisplatin treatment at different time points accompanied
by lower incidence of lung metastasis compared with other groups. The
observation of Xenogen IVIS was confirmed by histopathological
examination. The HSC activation by D-SMA staining in the liver
tumors was suppressed by SAC and Cisplatin treatment accompanied
with less TAM infiltration. Consistent with in vivo study, in vitro
functional study also demonstrated that SAC not only induced cell
cycle arrest and tumor cell apoptosis, but also significantly sensitized
the anti-cancer effect of Cisplatin.
Conclusion: SAC treatment significantly inhibited liver tumor growth
and metastasis by induction of tumor cell apoptosis and together with
sensitization of chemotherapy. |
Persistent Identifier | http://hdl.handle.net/10722/108365 |
ISSN | 2023 Impact Factor: 5.9 2023 SCImago Journal Rankings: 1.813 |
PubMed Central ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Guo, D | en_HK |
dc.contributor.author | Ng, TP | en_HK |
dc.contributor.author | Cheng, Q | en_HK |
dc.contributor.author | Lim, ZXH | en_HK |
dc.contributor.author | Lam, TT | en_HK |
dc.contributor.author | Man, K | en_HK |
dc.date.accessioned | 2010-09-26T00:36:36Z | - |
dc.date.available | 2010-09-26T00:36:36Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | The 4th Hong Kong-Shanghai International Liver Congress (ILC 2008), Hong Kong, 12–15 June 2008. In Hepatology International, 2008, v. 2 suppl. 2, p. S105 | - |
dc.identifier.issn | 1936-0533 | - |
dc.identifier.uri | http://hdl.handle.net/10722/108365 | - |
dc.description.abstract | Background and Objective: A garlic derivative S-allylcysteine (SAC) has anti-cancer effect in human prostate and colon cancers. We aimed to investigate the effect of SAC and combination of chemo-drug on tumorigenesis and metastasis of liver cancer. Materials and Methods: The orthotopic liver tumor model using a metastatic liver cancer cell line MHCC97L labeled with luciferase gene was applied. SAC was given at day 7 after tumor implantation at 1mg/g/day, 2mg/g/day, or 1mg/g/day combined with low dose Cisplatin for 5 weeks. Tumor growth and metastasis were monitored by Xenogen in vivo imaging system. Hepatic stellate cell (HSC) activation and tumor-associated macrophage (TAM) in the tumor tissue were detected by D-SMA and ED1/ED2 staining. Tumor micro-vessel density (MVD) and apoptosis were also analyzed. In vitro functional tests including MTT assay, colony formation assay, cell cycle analysis and apoptosis analysis were performed. Results: The tumor growth was significantly inhibited by SAC combined with Cisplatin treatment at different time points accompanied by lower incidence of lung metastasis compared with other groups. The observation of Xenogen IVIS was confirmed by histopathological examination. The HSC activation by D-SMA staining in the liver tumors was suppressed by SAC and Cisplatin treatment accompanied with less TAM infiltration. Consistent with in vivo study, in vitro functional study also demonstrated that SAC not only induced cell cycle arrest and tumor cell apoptosis, but also significantly sensitized the anti-cancer effect of Cisplatin. Conclusion: SAC treatment significantly inhibited liver tumor growth and metastasis by induction of tumor cell apoptosis and together with sensitization of chemotherapy. | - |
dc.language | eng | en_HK |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://www.springer.com/west/home/medicine?SGWID=4-10054-70-173733513-0 | - |
dc.relation.ispartof | Hepatology International | en_HK |
dc.title | A garlic derivative S-allylcysteine suppresses liver tumor growth and metastasis by sensitizing chemotherapy | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Ng, TP: ledodes@hku.hk | en_HK |
dc.identifier.email | Cheng, Q: qiaocheng@hotmail.com | en_HK |
dc.identifier.email | Lim, ZXH: zophialim@gmail.com | en_HK |
dc.identifier.email | Lam, TT: ttlams@hotmail.com | en_HK |
dc.identifier.email | Man, K: kwanman@hkucc.hku.hk | en_HK |
dc.identifier.authority | Man, K=rp00417 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1007/s12072-008-9079-9 | - |
dc.identifier.pmcid | PMC2716912 | - |
dc.identifier.hkuros | 144224 | en_HK |
dc.identifier.volume | 2 | - |
dc.identifier.issue | suppl. 2 | - |
dc.identifier.spage | S105 | - |
dc.identifier.epage | S105 | - |
dc.identifier.issnl | 1936-0533 | - |