Beneficial effects of a medicinal herb,Cirsium japonicum var. maackii,extract and its major component,cirsimaritin on breast cancer metastasis in MDA-MB-231 breast cancer cells |
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Authors: | Jun Yeon Park Hyun Young Kim Takayuki Shibamoto Tae Su Jang Sang Cheon Lee Jae Suk Shim Dae-Hyun Hahm Hae-Jeung Lee Sanghyun Lee Ki Sung Kang |
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Affiliation: | 1. College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea;2. Department of Food Science, Gyeongnam National University of Science and Technology, Jinju 52725, Republic of Korea;3. Department of Environmental Toxicology, University of California, Davis, CA 95616, USA;4. Institute of Green Bio Science & Technology, Seoul National University, Pyeong Chang 232-916, Republic of Korea;5. Imsil Research Institute of Cheese Science, Imsil 566-881, Republic of Korea;6. Imsil Herbal Medicine Association, Imsil 55955, Republic of Korea;7. Department of Physiology, College of Medicine, Kyung Hee University, 26 Kyungheedae-ro Dongdaemun-gu, Seoul 02447, Republic of Korea;8. Department of Food and Nutrition, College of BioNano Technology, Gachon University, Seongnam 13120, Republic of Korea;9. Department of Integrative Plant Science, Chung-Ang University, Anseong 17546, Republic of Korea |
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Abstract: | The biological activities of the ethanol extract from Cirsium japonicum var. maackii (ICF-1) and its major component, polyphenol cirsimaritin, were investigated as part of the search for possible alternative drugs for breast cancer. Three in vitro cell-based assays were used: the cell proliferation assay, tube-formation assay, and Western blot analysis. Both the ICF-1 extract and cirsimaritin inhibited the viability of HUVECs in a dose-dependent manner. The inhibition achieved was 36.89% at a level of 200 μg/ml by the ICF-1 extract and 62.04% at a level of 100 μM by cirsimaritin. The ICF-1 extract and cirsimaritin reduced tube formation by 12.69% at level of 25 μg/ml and 32.18% at the levels of 6.25 μM, respectively. Cirsimaritin inhibited angiogenesis by downregulation of VEGF, p-Akt and p-ERK in MDA-MB-231 cells, suggesting that cirsimaritin is potentially useful as an anti-metastatic agent. The present study demonstrated that Cirsium japonicum extract and its active component cirsimaritin is an excellent candidate as an alternative anti-breast cancer drug. |
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Keywords: | Cirsimaritin Breast cancer Metastasis Natural plant extract |
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