Abstract |
Ivalin, an eudesmane-type sesquiterpene compound, was isolated from the Chinese herb Carpesium divaricatum in our chemistry group. In this study, we investigated the anti-migration and anti-invasion activities and underlying mechanisms of Ivalin in breast cancer cells in vitro. Cell viability was evaluated using the MTT assay, Western blotting was used to determine the expression of E-cadherin, N-cadherin, vimentin and ZEB1, and mRNA levels were analyzed by qPCR. The anti-migration and anti-invasion effects of Ivalin were measured by wound-healing and Transwell assays. In this connection, Ivalin treatment reduced the mRNA and protein expressions of ZEB1 as well as N-cadherin and vimentin expression in various breast cancer cells. E-cadherin expression was enhanced by Ivalin in the same cells, which implied that Ivalin depressed the process of epithelial-to-mesenchymal transition (EMT). Our results revealed that Ivalin significantly inhibited cell proliferation, migration and invasion in breast cancer cells in a dose-dependent manner in vitro. This study suggests that Ivalin may merit further investigation as a potential therapeutic leading compound for the treatment of breast cancer migration and invasion.
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Authors | Jia-Hui Ma, Jie Qi, Fang-Yuan Liu, Shi-Qi Lin, Cai-Yun Zhang, Wei-Dong Xie, Hang-Yu Zhang, Xia Li |
Journal | Nutrition and cancer
(Nutr Cancer)
2018 Nov-Dec
Vol. 70
Issue 8
Pg. 1330-1338
ISSN: 1532-7914 [Electronic] United States |
PMID | 30463445
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Video-Audio Media)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Lactones
- Sesquiterpenes
- ivalin
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Topics |
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Breast Neoplasms
(drug therapy, pathology)
- Cell Line, Tumor
- Cell Movement
(drug effects)
- Cell Proliferation
(drug effects)
- Epithelial-Mesenchymal Transition
(drug effects, physiology)
- Female
- Gene Expression Regulation, Neoplastic
(drug effects)
- Humans
- Lactones
(pharmacology)
- Sesquiterpenes
(pharmacology)
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