Modulation of CXCR4, CXCL12, and Tumor Cell Invasion Potential In Vitro by Phytochemicals

被引:24
|
作者
Hsu, Erin L. [1 ,2 ,3 ]
Chen, Natalie [2 ,4 ]
Westbrook, Aya [1 ,2 ,4 ]
Wang, Feng [2 ,4 ]
Zhang, Ruixue [2 ,4 ]
Taylor, Robert T. [1 ,2 ,5 ]
Hankinson, Oliver [1 ,2 ,4 ]
机构
[1] Univ Calif Los Angeles, Mol Toxicol Interdept Doctoral Program, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[3] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[4] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[5] CellzDirect Invitrogen Corp, Dept Hepat Biol, Austin, TX 78754 USA
关键词
D O I
10.1155/2009/491985
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CXCR4 is a chemokine receptor frequently overexpressed on primary tumor cells. Organs to which these cancers metastasize secrete CXCL12, the unique ligand for CXCR4, which stimulates invasion and metastasis to these sites. Similar to our previous work with the chemoprotective phytochemical, 3,3' -diindolylmethane (DIM), we show here that genistein also downregulates CXCR4 and CXCL12 and subsequently lowers the migratory and invasive potentials of breast and ovarian cancer cells. Moreover, genistein and DIM elicit a significantly greater cumulative effect in lowering CXCR4 and CXCL12 levels than either compound alone. Our data suggest a novel mechanism for the protective effects of phytochemicals against cancer progression and indicate that in combination, these compounds may prove even more efficacious. Copyright (C) 2009 Erin L. Hsu et al.
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页数:9
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