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Red American ginseng enhances the effect of fluorouracil on human colon cancer cells via both paraptosis and apoptosis pathways
Jin-Yi Wan, Haiqiang Yao, Chun-Feng Zhang, Wei-Hua Huang, Qihui Zhang, Zhi Liu, Yi Bi, Stephanie Willimas, Chong-Zhi Wang, Chun-Su Yuan
Jazyk angličtina Země Česko
Typ dokumentu práce podpořená grantem
- MeSH
- apoptóza účinky léků MeSH
- fluoruracil aplikace a dávkování farmakologie MeSH
- ginsenosidy aplikace a dávkování farmakologie MeSH
- kolorektální nádory farmakoterapie MeSH
- kombinovaná farmakoterapie MeSH
- nádorové buňky kultivované účinky léků MeSH
- screeningové testy protinádorových léčiv MeSH
- synergismus léků MeSH
- techniky in vitro MeSH
- ženšen chemie MeSH
- Publikační typ
- práce podpořená grantem MeSH
Introduction As a commonly used chemotherapeutic agent, fluorouracil (5-FU) has serious dose-limiting side effects. In this study, we evaluated the synergy between red American ginseng (RAG) and 5-FU on human colorectal cancer cells, and explored the potential mechanisms. Methods Ginsenoside contents of white American ginseng (WAG) and RAG were determined by HPLC. Cell proliferation was evaluated by MTS assay. Combination Index (CI) analysis was executed using CompuSyn software. Paraptotic events were observed after crystal violet staining. Cell cycle distribution, cyclin A expression and apoptotic induction were analyzed using flow cytometry. Results We observed the heat treatment remarkably increased levels of ginsenoside Rg3, 20R-Rg3, Rk1 and Rg5. When the combinations of 5-FU and RAG were applied, cell proliferation inhibition rates were notably increased, indicating that RAG significantly enhanced 5-FU’s effect. Additionally, CI analysis suggested that there was a synergistic action of 5-FU and RAG when combined. The cell cycle data indicated 5-FU induced S phase arrest, and the combination of 5-FU and RAG increased G1 phase. Further, the RAG’s ability to enhance the anti-cancer effects of 5-FU was linked to both paraptosis and apoptosis inductions.
Jiangsu University School of Pharmacy Zhenjiang China
University of Chicago Comprehensive Cancer Center Chicago USA
University of Chicago Department of Anesthesia and Critical Care Chicago USA
University of Chicago Tang Center for Herbal Medicine Research Chicago USA
Citace poskytuje Crossref.org
Literatura
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- $a Introduction As a commonly used chemotherapeutic agent, fluorouracil (5-FU) has serious dose-limiting side effects. In this study, we evaluated the synergy between red American ginseng (RAG) and 5-FU on human colorectal cancer cells, and explored the potential mechanisms. Methods Ginsenoside contents of white American ginseng (WAG) and RAG were determined by HPLC. Cell proliferation was evaluated by MTS assay. Combination Index (CI) analysis was executed using CompuSyn software. Paraptotic events were observed after crystal violet staining. Cell cycle distribution, cyclin A expression and apoptotic induction were analyzed using flow cytometry. Results We observed the heat treatment remarkably increased levels of ginsenoside Rg3, 20R-Rg3, Rk1 and Rg5. When the combinations of 5-FU and RAG were applied, cell proliferation inhibition rates were notably increased, indicating that RAG significantly enhanced 5-FU’s effect. Additionally, CI analysis suggested that there was a synergistic action of 5-FU and RAG when combined. The cell cycle data indicated 5-FU induced S phase arrest, and the combination of 5-FU and RAG increased G1 phase. Further, the RAG’s ability to enhance the anti-cancer effects of 5-FU was linked to both paraptosis and apoptosis inductions.
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