Kaempferol suppresses cell metastasis via inhibition of the ERK-p38-JNK and AP-1 signaling pathways in U-2 OS human osteosarcoma cells

被引:105
作者
Chen, Hui-Jye [1 ]
Lin, Chung-Ming [5 ]
Lee, Chao-Ying [2 ]
Shih, Nai-Chen [3 ]
Peng, Shu-Fen [4 ]
Tsuzuki, Minoru [6 ]
Amagaya, Sakae [7 ]
Huang, Wen-Wen [4 ]
Yang, Jai-Sing [3 ]
机构
[1] China Med Univ, Grad Inst Mol Syst Biomed, Taichung 40402, Taiwan
[2] China Med Univ, Sch Pharm, Taichung 40402, Taiwan
[3] China Med Univ, Dept Pharmacol, Taichung 40402, Taiwan
[4] China Med Univ, Dept Biol Sci & Technol, Taichung 40402, Taiwan
[5] Ming Chuan Univ, Dept Biotechnol, Tao Yuan 333, Taiwan
[6] Nihon Pharmaceut Univ, Dept Biochem, Ina, Saitama 3620806, Japan
[7] Nihon Pharmaceut Univ, Dept Kampo Pharmaceut Sci, Ina, Saitama 3620806, Japan
关键词
kaempferol; metastasis; ERK; p38; JNK; AP-1; U-2 osteosarcoma cells; UROKINASE-PLASMINOGEN-ACTIVATOR; NF-KAPPA-B; CAVITY CANCER-CELLS; MATRIX METALLOPROTEINASES; C-FOS; TRANSCRIPTIONAL ACTIVITY; ANTIOXIDANT ACTIVITY; MURAMYL TRIPEPTIDE; OXIDATIVE STRESS; CARCINOMA-CELLS;
D O I
10.3892/or.2013.2490
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Kaempferol is a natural flavonoid that possesses anti-proliferative and apoptosis-inducing activities in several cancer cell lines. In the present study, we investigated the anti-metastatic activity of kaempferol and its molecular mechanism(s) of action in human osteosarcoma cells. Kaempferol displayed inhibitory effects on the invasion and adhesion of U-2 osteosarcoma (OS) cells in a concentration-dependent manner by Matrigel Transwell assay and cell adhesion assay. Kaempferol also inhibited the migration of U-2 OS cells in a concentration-dependent manner at different treatment time points by wound-healing assay. Additional experiments showed that kaempferol treatment reduced the enzymatic activities and protein levels of matrix metalloproteinase (MMP)-2, MMP-9 and urokinase plasminogen activator (uPA) by gelatin and casein-plasminogen zymography assays and western blot analyses. Kaempferol also downregulated the mRNA levels of MMP-2 and MMP-9 by quantitative PCR analyses. Furthermore, kaempferol was able to reduce the protein phosphorylation of ERK, p38 and JNK by western blotting. By electrophoretic mobility-shift assay (EMSA), we demonstrated that kaempferol decreased the DNA binding activity of AP-1, an action likely to result in the reduced expression of MMP-2, MMP-9 and uPA. Collectively, our data showed that kaempferol attenuated the MAPK signaling pathways including ERK, JNK and p38 and resulted in the decreased DNA binding ability of AP-1, and hence, the downregulation in the expression and enzymatic activities of MMP-2, MMP-9 and uPA, contributing to the inhibition of metastasis of U-2 OS cells. Our results suggest a potential role of kaempferol in the therapy of tumor metastasis of OS.
引用
收藏
页码:925 / 932
页数:8
相关论文
共 74 条
[1]   Phenolic contents and antioxidant activity of some food and medicinal plants [J].
Bajpai, M ;
Pande, A ;
Tewari, SK ;
Prakash, D .
INTERNATIONAL JOURNAL OF FOOD SCIENCES AND NUTRITION, 2005, 56 (04) :287-291
[2]   Matrix metalloproteinases participate in osteosarcoma invasion [J].
Bjornland, K ;
Flatmark, K ;
Pettersen, S ;
Aaasen, AO ;
Fodstad, O ;
Maelandsmo, GM .
JOURNAL OF SURGICAL RESEARCH, 2005, 127 (02) :151-156
[3]   Antioxidant and antiradical activities of flavonoids [J].
Burda, S ;
Oleszek, W .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (06) :2774-2779
[4]   A Review on the Dietary Flavonoid Kaempferol [J].
Calderon-Montano, J. M. ;
Burgos-Moron, E. ;
Perez-Guerrero, C. ;
Lopez-Lazaro, M. .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2011, 11 (04) :298-344
[5]   Antitumor activity of some natural flavonoids and synthetic derivatives on various human and murine cancer cell lines [J].
Cárdenas, M ;
Marder, M ;
Blank, VC ;
Roguin, LP .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (09) :2966-2971
[6]   Changing views of the role of matrix metalloproteinases in metastasis [J].
Chambers, AF ;
Matrisian, LM .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (17) :1260-1270
[7]   The novel synthesized 6-fluoro-(3-fluorophenyl)-4-(3-methoxyanilino)quinazoline (LJJ-10) compound exhibits anti-metastatic effects in human osteosarcoma U-2 OS cells through targeting insulin-like growth factor-I receptor [J].
Chen, Kuan-Tin ;
Hour, Mann-Jen ;
Tsai, Shih-Chang ;
Chung, Jing-Gung ;
Kuo, Sheng-Chu ;
Lu, Chi-Cheng ;
Chiu, Yu-Jen ;
Chuang, Yi-Hsuan ;
Yang, Jai-Sing .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2011, 39 (03) :611-619
[8]   Silibinin inhibits cell invasion through inactivation of both PI3K-Akt and MAPK signaling pathways [J].
Chen, PN ;
Hsieh, YS ;
Chiou, HL ;
Chu, SC .
CHEMICO-BIOLOGICAL INTERACTIONS, 2005, 156 (2-3) :141-150
[9]   Novel Quinazoline HMJ-30 Induces U-2 OS Human Osteogenic Sarcoma Cell Apoptosis through Induction of Oxidative Stress and Up-Regulation of ATM/p53 Signaling Pathway [J].
Chiu, Yu-Jen ;
Hour, Mann-Jen ;
Lu, Chi-Cheng ;
Chung, Jing-Gung ;
Kuo, Sheng-Chu ;
Huang, Wen-Wen ;
Chen, Hui-Jye ;
Jin, Yi-An ;
Yang, Jai-Sing .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2011, 29 (09) :1448-1456
[10]   Urokinase plasminogen activator system - A multifunction role in tumor progression and metastasis [J].
Choong, PFM ;
Nadesapillai, APW .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2003, (415) :S46-S58