Abstract |
Colorectal cancer is one of the most common causes of cancer-related death in humans. Coptisine (COP) is a natural alkaloid from Coptidis Rhizoma with unclear antitumor mechanism. Human colon cancer cells (HCT-116) and xenograft mice were used to systematically explore the anti- tumor activity of COP in this study. The results indicated that COP exhibited remarkably cytotoxic activities against the HCT-116 cells by inducing G1-phase cell cycle arrest and increasing apoptosis, and preferentially inhibited the survival pathway and induced the activation of caspase proteases family of HCT-116 cells. Experimental results on male BALB/c nude mice confirmed that orally administration of COP at high-dose (150 mg/kg) could suppress tumor growth, and may reduce cancer metastasis risk by inhibiting the RAS-ERK pathway in vivo. Taken together, the results suggested that COP may be potential as a novel anti- tumor candidate in the HCT-116 cells-related colon cancer, further studies are still needed to suggest COP for the further use.
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Authors | Tao Huang, Yubo Xiao, Lin Yi, Ling Li, Meimei Wang, Cheng Tian, Hang Ma, Kai He, Yue Wang, Bing Han, Xiaoli Ye, Xuegang Li |
Journal | Scientific reports
(Sci Rep)
Vol. 7
Pg. 38524
(02 06 2017)
ISSN: 2045-2322 [Electronic] England |
PMID | 28165459
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- coptisine
- Berberine
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Topics |
- Administration, Oral
- Animals
- Antineoplastic Agents
(administration & dosage, isolation & purification, pharmacology)
- Araceae
(chemistry)
- Berberine
(administration & dosage, analogs & derivatives, isolation & purification, pharmacology)
- Cell Proliferation
(drug effects)
- Colorectal Neoplasms
(drug therapy, pathology)
- Disease Models, Animal
- HCT116 Cells
(drug effects)
- Heterografts
- Humans
- Mice, Inbred BALB C
- Mice, Nude
- Neoplasm Transplantation
- Treatment Outcome
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