Caffeic Acid Phenethyl Ester Inhibits Oral Cancer Cell Metastasis by Regulating Matrix Metalloproteinase-2 and the Mitogen-Activated Protein Kinase Pathway

Author:

Peng Chih-Yu12,Yang Hui-Wen12,Chu Yin-Hung3,Chang Yu-Chao12,Hsieh Ming-Ju4,Chou Ming-Yung12,Yeh Kun-Tu5,Lin Yueh-Min5,Yang Shun-Fa36,Lin Chiao-Wen27

Affiliation:

1. School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan

2. Department of Dentistry, Chung Shan Medical University Hospital, Taichung 40201, Taiwan

3. Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan

4. School of Medical Laboratory and Biotechnology, Chung Shan Medical University, Taichung 40201, Taiwan

5. Department of Pathology, Changhua Christian Hospital, Changhua 50006, Taiwan

6. Department of Medical Research, Chung Shan Medical University Hospital, Taichung 40201, Taiwan

7. Institute of Oral Sciences, Chung Shan Medical University, Taichung 40201, Taiwan

Abstract

Caffeic acid phenethyl ester (CAPE), an active component extracted from honeybee hives, exhibits anti-inflammatory and anticancer activities. However, the molecular mechanism by which CAPE affects oral cancer cell metastasis has yet to be elucidated. In this study, we investigated the potential mechanisms underlying the effects of CAPE on the invasive ability of SCC-9 oral cancer cells. Results showed that CAPE attenuated SCC-9 cell migration and invasion at noncytotoxic concentrations (0 μM to 40 μM). Western blot and gelatin zymography analysis findings further indicated that CAPE downregulated matrix metalloproteinase-2 (MMP-2) protein expression and inhibited its enzymatic activity. CAPE exerted its inhibitory effects on MMP-2 expression and activity by upregulating tissue inhibitor of metalloproteinase-2 (TIMP-2) and potently decreased migration by reducing focal adhesion kinase (FAK) phosphorylation and the activation of its downstream signaling molecules p38/MAPK and JNK. These data indicate that CAPE could potentially be used as a chemoagent to prevent oral cancer metastasis.

Funder

National Science Council

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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