| Literature DB >> 31010399 |
Ming-Jie Hsu1, Shu-Fen Peng1,2, Fu-Shin Chueh3, Chang-Hai Tsai4,5, Fuu-Jen Tsai4,6, Chih-Yang Huang7,8,9, Chih-Hsin Tang9,10,11, Jai-Sing Yang12, Yuan-Man Hsu1, Wen-Wen Huang1, Jing-Gung Chung1,9.
Abstract
Lupeol, one of the common components from the fruits and natural foods, has been reported to exert antitumor activities in many human cancer cell lines; however, its effects on osteosarcoma cell metastasis were not elucidated. In the present study, lupeol at 10-25 μM induced cell morphological changes and decreased total viable cell number in U-2 OS cells. Lupeol (5-15 μM) suppressed cell mobility, migration, and invasion by wound healing and transwell chamber assays, respectively. Lupeol inhibited the activities of MMP-2 and -9 in U-2 OS cells by gelatin zymography assay. Lupeol significantly decreased PI3K, pAKT, β-catenin, and increased GSK3β. Furthermore, lupeol decreased the expressions of Ras, p-Raf-1, p-p38, and β-catenin. Lupeol also decreased uPA, MMP-2, MMP-9, and N-cadherin but increased VE-cadherin in U-2 OS cells. Based on these observations, we suggest that lupeol can be used in anti-metastasis of human osteosarcoma cells in the future.Entities:
Keywords: Lupeol; human osteosarcoma U-2 OS cell; invasion; migration; p38 MAPK signaling pathway
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Year: 2019 PMID: 31010399 DOI: 10.1080/09168451.2019.1606693
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043