Inhibition of Human Breast Cancer Xenograft Growth by Cruciferous Vegetable Constituent Benzyl Isothiocyanate

被引:56
作者
Warin, Renaud [1 ]
Xiao, Dong [1 ]
Arlotti, Julie A. [1 ]
Bommareddy, Ajay [1 ]
Singh, Shivendra V. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Pharmacol & Chem Biol, Inst Canc, Pittsburgh, PA USA
关键词
breast cancer; isothiocyanate; VEGF receptor; angiogenesis; A/J MICE; TUMOR ANGIOGENESIS; LUNG TUMORIGENESIS; PROSTATE-CANCER; IN-VIVO; PREVENTION; APOPTOSIS; 4-(METHYLNITROSAMINO)-1-(3-PYRIDYL)-1-BUTANONE; DIETHYLNITROSAMINE; METABOLISM;
D O I
10.1002/mc.20600
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Benzyl isothiocyanate (BITC), a constituent of cruciferous vegetables such as garden cress, inhibits growth of human breast cancer cell lines in culture. The present study was undertaken to determine in vivo efficacy of BITC against MDA-MB-231 human breast cancer xenografts. The BITC administration retarded growth of MDA-MB-231 cells subcutaneously implanted in female nude mice without causing weight loss or any other side effects. The BITC-mediated suppression of MDA-MB-231 xenograft growth correlated with reduced cell proliferation as revealed by immunohistochemical analysis for Ki-67 expression. Analysis of the vasculature in the tumors from BITC-treated mice indicated smaller vessel area compared with control tumors based on immunohistochemistry for angiogenesis marker CD31. The BITC-mediated inhibition of angiogenesis in vivo correlated with downregulation of vascular endothelial growth factor (VEGF) receptor 2 protein levels in the tumor. Consistent with these results, BITC treatment suppressed VEGF secretion and VEGF receptor 2 protein levels in cultured MDA-MB-231 cells. Moreover, the BITC-treated MDA-MB-231 cells exhibited reduced capacity for migration compared with vehicle-treated control cells. In contrast to cellular data, BITC administration failed to elicit apoptotic response as judged by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay. In conclusion, the present study demonstrates in vivo anti-cancer efficacy of BITC against MDA-MB-231 xenografts in association with reduced cell proliferation and suppression of neovascularization. These preclinical observations merit clinical investigation to determine efficacy of BITC against human breast cancers. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:500 / 507
页数:8
相关论文
共 36 条
[1]   Breast cancer risk in premenopausal women is inversely associated with consumption of broccoli, a source of isothiocyanates, but is not modified by GST genotype [J].
Ambrosone, CB ;
McCann, SE ;
Freudenheim, JL ;
Marshall, JR ;
Zhang, YS ;
Shields, PG .
JOURNAL OF NUTRITION, 2004, 134 (05) :1134-1138
[2]   Effects of benzyl isothiocyanate and 2-phenethyl isothiocyanate on benzo[a]pyrene and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone metabolism in F-344 rats [J].
Boysen, G ;
Kenney, PMJ ;
Upadhyaya, P ;
Wang, MY ;
Hecht, SS .
CARCINOGENESIS, 2003, 24 (03) :517-525
[3]  
BROWN LF, 1993, CANCER RES, V53, P4727
[4]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[5]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[6]   Isothiocyanates as cancer chemopreventive agents: Their biological activities and metabolism in rodents and humans [J].
Conaway, CC ;
Yang, YM ;
Chung, FL .
CURRENT DRUG METABOLISM, 2002, 3 (03) :233-255
[7]  
Cuzick J, 2002, LANCET, V360, P817
[8]   Optical imaging of the breast [J].
de Ven, S. M. W. Y. van ;
Elias, S. G. ;
van den Bosch, M. A. A. J. ;
Luijten, P. ;
Mali, W. P. Th. M. .
CANCER IMAGING, 2008, 8 (01) :206-215
[9]   Temporal trends in breast cancer mortality by state and race [J].
DeSantis, Carol ;
Jemal, Ahmedin ;
Ward, Elizabeth ;
Thun, Michael J. .
CANCER CAUSES & CONTROL, 2008, 19 (05) :537-545
[10]  
Dhanabal Mohanraj, 2005, Current Medicinal Chemistry - Anti-Cancer Agents, V5, P115, DOI 10.2174/1568011053174882