α-Lipoic acid reduces matrix metalloproteinase activity in MDA-MB-231 human breast cancer cells

被引:46
作者
Lee, Hyun Sook [2 ]
Na, Mi Hee [1 ]
Kim, Woo Kyoung [1 ]
机构
[1] Dankook Univ, Dept Food Sci & Nutr, Yongin 448701, Gyeonggi Do, South Korea
[2] Kookmin Univ, Dept Foods & Nutr, Seoul 136702, South Korea
关键词
alpha-Lipoic acid; Metastasis; Breast cancer cells; MMP-2; MMP-9; TUMOR INVASION; ANTIOXIDANT; MIGRATION; EXPRESSION; RISK; CHEMOPREVENTION; PROLIFERATION; SUPPRESSION; INHIBITORS; APOPTOSIS;
D O I
10.1016/j.nutres.2010.06.009
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
alpha-Lipoic acid (LA), a naturally occurring molecule in animal and plant cells, is a potent antioxidant that reportedly exerts beneficial effects on cell proliferation and apoptosis in various cancer cell lines. However, the molecular mechanisms behind the antimetastatic property of LA are not well understood. The present study investigates the effect of LA on metastasis in a cell system. Our hypothesis is that LA inhibits metastasis via inhibition of matrix metalloproteinase (MMP) in vitro. MDA-MB-231 cells, a human breast cancer cell line, were treated with various concentrations of LA (0, 250, 500, or 1000 mol/L) to measure metastasis, MMP activity, and mRNA expression. The viability of cells was examined by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay. The effect of LA on metastasis was evaluated using the motility, migration, and invasion assay in vitro. The activity and mRNA expression of MMP-2 and MMP-9 were measured. After LA treatment, cell motility and cell migration were significantly decreased (P < .05). alpha-Lipoic acid also reduced cell invasion through a Matrigel-coated chamber (P < .05). Activities of MMP-2 and MMP-9 were decreased by LA treatment in a dose-dependent manner. RT-PCR analysis confirmed the reduction in mRNA expression level of MMP-2 and MMP-9 by LA treatment. We conclude that in this cell culture model, LA treatment inhibits cancer metastasis, and this inhibition is likely due to the decrease in the activity and mRNA expression levels of MMP-2 and MMP-9 caused by LA. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:403 / 409
页数:7
相关论文
共 37 条
[1]   The long-term survival of a patient with pancreatic cancer with metastases to the liver after treatment with the intravenous α-lipoic acid/low-dose naltrexone protocol [J].
Berkson, Burton M. ;
Rubin, Daniel M. ;
Berkson, Arthur J. .
INTEGRATIVE CANCER THERAPIES, 2006, 5 (01) :83-89
[2]   Tissue inhibitors of metalloproteinases: evolution, structure and function [J].
Brew, K ;
Dinakarpandian, D ;
Nagase, H .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2) :267-283
[3]   Effects of α-lipoic acid on neurovascular function in diabetic rats:: interaction with essential fatty acids [J].
Cameron, NE ;
Cotter, MA ;
Horrobin, DH ;
Tritschler, HJ .
DIABETOLOGIA, 1998, 41 (04) :390-399
[4]   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
[5]  
CHEN J, 2007, BREAST CANC RES COMM, V254, P739
[6]   Protection against arsenic trioxide-induced autophagic cell death in U118 human glioma cells by use of lipoic acid [J].
Cheng, Tain-Junn ;
Wang, Ying-Jan ;
Kao, Wei-Wan ;
Chen, Rong-Jane ;
Ho, Yuan-Soon .
FOOD AND CHEMICAL TOXICOLOGY, 2007, 45 (06) :1027-1038
[7]   Conjugated linoleic acid inhibits cell proliferation and ErbB3 signaling in HT-29 human colon cell line [J].
Cho, HJ ;
Kim, WK ;
Kim, EJ ;
Jung, KC ;
Park, S ;
Lee, HS ;
Tyner, AL ;
Park, JHY .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (06) :G996-G1005
[8]   Matrix metalloproteinases: molecular aspects of their roles in tumour invasion and metastasis [J].
Curran, S ;
Murray, GI .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (13) :1621-1630
[9]   Inhibitory effect of emodin on tumor invasion through suppression of activator protein-1 and nuclear factor-κB [J].
Huang, Q ;
Shen, HM ;
Ong, CN .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (02) :361-371
[10]   Fruit and vegetable intake and risk of major chronic disease [J].
Hung, HC ;
Joshipura, KJ ;
Jiang, R ;
Hu, FB ;
Hunter, D ;
Smith-Warner, SA ;
Colditz, GA ;
Rosner, B ;
Spiegelman, D ;
Willett, WC .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (21) :1577-1584