Quercetin and sulforaphane in combination suppress the progression of melanoma through the down-regulation of matrix metalloproteinase-9

被引:44
作者
Pradhan, Saurabh J. [1 ]
Mishra, Rosalin [1 ]
Sharma, Priyanka [1 ]
Kundu, Gopal C. [1 ]
机构
[1] Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
关键词
quercetin; sulforaphane; matrix metalloproteinase-9; melanoma growth; PROSTATE-CANCER CELLS; TUMOR-GROWTH; PROMATRIX METALLOPROTEINASE-2; MATRIX-METALLOPROTEINASE; PC-3; XENOGRAFTS; STROMAL CELLS; CRUCIAL ROLE; ACTIVATION; APOPTOSIS; INHIBITION;
D O I
10.3892/etm.2010.144
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Malignant melanoma is one of the most common types of cancer in the US and worldwide. The epidemiological data suggest that dietary modification may reduce the incidence of this disease. Quercetin (3,5,7,3',4'-tetra-hydroxyflavone), a flavonoid isolated from onion, exhibits anti-oxidant, anti-inflammatory and anti-cancer effects. D,L-sulforaphane [1-isothiocyanato-4-(methylsulfinyl)butane], a cruciferous vegetable-derived isomer isolated from broccoli, is highly effective in protection against cancer. Matrix metalloproteinases (MMPs), extracellular matrix degrading enzymes, are involved in embryogenesis, inflammation, angiogenesis and cancer. MMP-9 in particular plays a crucial role in the regulation of invasion, tumor growth and metastasis. Previous studies have reported that both quercetin and sulforaphane independently reduce tumor growth and metastasis in breast, prostate, lung and other types of cancers. However, the combined effects of quercetin and sulforaphane on the regulation of tumor growth and the mechanism(s) of actions underlying this process have not yet been investigated. In the present study, we report for the first time that quercetin and sulforaphane in combination inhibit the proliferation and migration of melanoma (B16F10) cells more effectively than either compound used alone. Moreover, these compounds in combination significantly suppressed melanoma growth as compared to their individual use in a mouse model. This combined effect was predominantly due to a decrease in MMP-9 expression in the mouse tumors. Taken together, our findings revealed that the administration of quercetin and sulforaphane in combination rather than alone may be a more effective approach for the treatment of malignant melanoma.
引用
收藏
页码:915 / 920
页数:6
相关论文
共 35 条
[1]   Molecular targets of dietary agents for prevention and therapy of cancer [J].
Aggarwal, BB ;
Shishodia, S .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (10) :1397-1421
[2]  
AVILA MA, 1994, CANCER RES, V54, P2424
[3]   Bcl-2 antisense (oblimersen sodium) plus dacarbazine in patients with advanced melanoma: The oblimersen melanoma study group [J].
Bedikian, Agop Y. ;
Millward, Michael ;
Pehamberger, Hubert ;
Conry, Robert ;
Gore, Martin ;
Trefzer, Uwe ;
Pavlick, Anna C. ;
DeConti, Ronald ;
Hersh, Evan M. ;
Hersey, Peter ;
Kirkwood, John M. ;
Haluska, Frank G. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (29) :4738-4745
[4]   Activation of JAK2/STAT3 signaling by osteopontin promotes tumor growth in human breast cancer cells [J].
Behera, Reeti ;
Kumar, Vinit ;
Lohite, Kirti ;
Karnik, Swapnil ;
Kundu, Gopal C. .
CARCINOGENESIS, 2010, 31 (02) :192-200
[5]   Antiproliferative effect of quercetin in the human U138MG glioma cell line [J].
Braganhol, Elizandra ;
Zamin, Lauren L. ;
Delgado Canedo, Andres ;
Horn, Fabiana ;
Tamajusuku, Alessandra S. K. ;
Wink, Marcia R. ;
Salbego, Christianne ;
Battastini, Ana M. O. .
ANTI-CANCER DRUGS, 2006, 17 (06) :663-671
[6]   Osteopontin promotes vascular endothelial growth factor-dependent breast tumor growth and angiogenesis via autocrine and paracrine mechanisms [J].
Chakraborty, Goutam ;
Jain, Shalini ;
Kundu, Gopal C. .
CANCER RESEARCH, 2008, 68 (01) :152-161
[7]   Bax and Bak are required for apoptosis induction by sulforaphane, a cruciferous vegetable-derived cancer chemopreventive agent [J].
Choi, S ;
Singh, SV .
CANCER RESEARCH, 2005, 65 (05) :2035-2043
[8]   MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis [J].
Coussens, LM ;
Tinkle, CL ;
Hanahan, D ;
Werb, Z .
CELL, 2000, 103 (03) :481-490
[9]   Dietary histone deacetylase inhibitors: From cells to mice to man [J].
Dashwood, Roderick H. ;
Ho, Emily .
SEMINARS IN CANCER BIOLOGY, 2007, 17 (05) :363-369
[10]   Melanoma biology and new targeted therapy [J].
Gray-Schopfer, Vanessa ;
Wellbrock, Claudia ;
Marais, Richard .
NATURE, 2007, 445 (7130) :851-857