Inhibition of cancer cell invasion and metastasis by genistein

被引:218
作者
Pavese, Janet M. [1 ,2 ]
Farmer, Rebecca L. [1 ,2 ,3 ]
Bergan, Raymond C. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Robert H Lurie Canc Ctr, Chicago, IL 60611 USA
[3] Northwestern Univ, Ctr Drug Discovery & Chem Biol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
Genistein; Metastasis; Invasion; Cancer; Chemoprevention; Adhesion; FOCAL ADHESION KINASE; HUMAN PROSTATE-CANCER; HEAT-SHOCK-PROTEIN; FACTOR-KAPPA-B; MATRIX-METALLOPROTEINASE TYPE-2; PURIFIED SOY ISOFLAVONES; ESTROGEN-RECEPTOR BETA; AKT SIGNALING PATHWAY; BREAST-CANCER; JAPANESE WOMEN;
D O I
10.1007/s10555-010-9238-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genistein is a small, biologically active flavonoid that is found in high amounts in soy. This important compound possesses a wide variety of biological activities, but it is best known for its ability to inhibit cancer progression. In particular, genistein has emerged as an important inhibitor of cancer metastasis. Consumption of genistein in the diet has been linked to decreased rates of metastatic cancer in a number of population-based studies. Extensive investigations have been performed to determine the molecular mechanisms underlying genistein's antimetastatic activity, with results indicating that this small molecule has significant inhibitory activity at nearly every step of the metastatic cascade. Reports have demonstrated that, at high concentrations, genistein can inhibit several proteins involved with primary tumor growth and apoptosis, including the cyclin class of cell cycle regulators and the Akt family of proteins. At lower concentrations that are similar to those achieved through dietary consumption, genistein can inhibit the prometastatic processes of cancer cell detachment, migration, and invasion through a variety of mechanisms, including the transforming growth factor (TGF)-beta signaling pathway. Several in vitro findings have been corroborated in both in vivo animal studies and in early-phase human clinical trials, demonstrating that genistein can both inhibit human cancer metastasis and also modulate markers of metastatic potential in humans, respectively. Herein, we discuss the variety of mechanisms by which genistein regulates individual steps of the metastatic cascade and highlight the potential of this natural product as a promising therapeutic inhibitor of metastasis.
引用
收藏
页码:465 / 482
页数:18
相关论文
共 183 条
[1]   Three-dimensional structure of the apoptosome: Implications for assembly, procaspase-9 binding, and activation [J].
Acehan, D ;
Jiang, XJ ;
Morgan, DG ;
Heuser, JE ;
Wang, XD ;
Akey, CW .
MOLECULAR CELL, 2002, 9 (02) :423-432
[2]   The Bcl-2 apoptotic switch in cancer development and therapy [J].
Adams, J. M. ;
Cory, S. .
ONCOGENE, 2007, 26 (09) :1324-1337
[3]   Ways of dying: multiple pathways to apoptosis [J].
Adams, JM .
GENES & DEVELOPMENT, 2003, 17 (20) :2481-2495
[4]   PLASMA-CONCENTRATIONS OF PHYTO-ESTROGENS IN JAPANESE MEN [J].
ADLERCREUTZ, H ;
MARKKANEN, H ;
WATANABE, S .
LANCET, 1993, 342 (8881) :1209-1210
[6]   URINARY-EXCRETION OF LIGNANS AND ISOFLAVONOID PHYTOESTROGENS IN JAPANESE MEN AND WOMEN CONSUMING A TRADITIONAL JAPANESE DIET [J].
ADLERCREUTZ, H ;
HONJO, H ;
HIGASHI, A ;
FOTSIS, T ;
HAMALAINEN, E ;
HASEGAWA, T ;
OKADA, H .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 54 (06) :1093-1100
[7]  
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[8]   Genistein-induced cell cycle arrest and apoptosis in a head and neck squamous cell carcinoma cell line [J].
Alhasan, SA ;
Pietrasczkiwicz, H ;
Alonso, MD ;
Ensley, J ;
Sarkar, FH .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 34 (01) :12-19
[9]  
Andersen O. M., 2006, FLAVONOIDS CHEM BIOC
[10]  
[Anonymous], 2007, BIOL CANC