Melittin suppresses EGF-induced cell motility and invasion by inhibiting PI3K/Akt/mTOR signaling pathway in breast cancer cells

被引:111
作者
Jeong, Yun-Jeong [1 ,2 ]
Choi, Yongsoo [3 ]
Shin, Jae-Moon [1 ,2 ,4 ]
Cho, Hyun-Ji [1 ,2 ]
Kang, Jeong-Han [1 ,2 ]
Park, Kwan-Kyu [1 ,2 ]
Choe, Jung-Yoon [1 ,2 ]
Bae, Young-Seuk [4 ]
Han, Sang-Mi [5 ]
Kim, Cheorl-Ho [6 ]
Chang, Hyeun-Wook [7 ]
Chang, Young-Chae [1 ,2 ]
机构
[1] Catholic Univ Daegu, Sch Med, Res Inst Biomed Engn, Taegu 705718, South Korea
[2] Catholic Univ Daegu, Sch Med, Dept Med, Taegu 705718, South Korea
[3] Korea Inst Sci & Technol, Natl Med Ctr, Kangnung 210340, South Korea
[4] Kyungpook Natl Univ, Sch Life Sci, Creat BioRes Grp, BK21 Plus Program, Taegu 702701, South Korea
[5] Natl Inst Agr Sci & Technol, Dept Agr Biol, Suwon 441100, Kyunggi Do, South Korea
[6] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, Kyunggi Do, South Korea
[7] Yeungnam Univ, Coll Pharm, Gyongsan 701947, South Korea
基金
新加坡国家研究基金会;
关键词
Bee venom; Melittin; FAK; MMP; Cancer invasion; FOCAL-ADHESION KINASE; NF-KAPPA-B; BEE VENOM; MMP-9; EXPRESSION; CARCINOMA-CELLS; OVARIAN-CANCER; MIGRATION; ACTIVATION; INDUCTION; RECEPTOR;
D O I
10.1016/j.fct.2014.03.022
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Bee venom is a natural compound produced by the honey bee (Apis mellifera), and has been reported as having the biological and pharmacological activities, including anti-bacterial, anti-viral and anti-inflammation. In the present study, the inhibitory effects of bee venom and its major peptide components on the tumor invasion were demonstrated. It was confirmed the inhibitory effects of bee venom, melittin, and apamin on the EGF-induced invasion of breast cancer cells. Transwell invasion and wound-healing assays showed that bee venom and melittin significantly inhibits the EGF-induced invasion and migration of breast cancer cells. Also, bee venom and melittin reduced the EGF-stimulated F-actin reorganization at the leading edge, but apamin did not affect. Particularly, melittin inhibited the EGF-induced MMP-9 expression via blocking the NF-kappa B and PI3K/Akt/mTOR pathway. In addition, melittin significantly suppressed the EGF-induced FAR phosphorylation through inhibition of mTOR/p70S6K/4E-BP1 pathway. These results suggest that inhibitory effects of melittin on breast cancer cell motility and migration may be related to the inhibition of mTOR pathway. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:218 / 225
页数:8
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