Natural Polyphenols that Display Anticancer Properties through Inhibition of Kinase Activity

被引:102
作者
Lamoral-Theys, D. [2 ]
Pottier, L. [1 ]
Dufrasne, F. [3 ]
Neve, J. [3 ]
Dubois, J. [2 ]
Kornienko, A. [4 ]
Kiss, R. [1 ]
Ingrassia, L. [1 ]
机构
[1] Univ Libre Bruxelles, Toxicol Lab, Inst Pharm, B-1050 Brussels, Belgium
[2] Univ Libre Bruxelles, Lab Chim Bioanalyt Toxicol & Chim Phys Appl, Inst Pharm, B-1050 Brussels, Belgium
[3] Univ Libre Bruxelles, Lab Chim Pharmaceut Organ, Inst Pharm, B-1050 Brussels, Belgium
[4] New Mexico Inst Min & Technol, Dept Chem, Socorro, NM 87801 USA
关键词
CELL-CYCLE ARREST; BREAST-CANCER CELLS; HEPATOCELLULAR-CARCINOMA CELLS; SIGNAL-TRANSDUCTION PATHWAYS; ACTIVATED PROTEIN-KINASE; INDUCED COX-2 EXPRESSION; GROWTH-FACTOR RECEPTOR; NECROSIS-FACTOR-ALPHA; BLACK TEA POLYPHENOL; HUMAN PROSTATE;
D O I
10.2174/092986710790712183
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
Over eleven hundred publications reporting anticancer activities of polyphenols have appeared in the peer-reviewed literature. In addition, a search of the PubMed database using "polyphenols - cancer - review" as keywords produced over 320 hits for review articles (July 2009). Polyphenol anticancer activities include, among others, anti-oxidative, pro-apoptotic, DNA damaging, anti-angiogenic, and immunostimulatory effects. Targeting specific protein kinases to combat cancer represents a major focus of oncology research within the so-called targeted therapy approach. An exhaustive search of the PubMed database (July 2009) using "polyphenols - cancer - kinases" as keywords resulted in more than 130 hits, half of them having been published within the past five years. Furthermore, the PubMed database contains 25 reviews on the subject of anti-kinase activity of some specific polyphenols, including mainly curcumin and the green tea polyphenol (-)- epigallocatechin 3-gallate (EGCG). However, no attempt has been made yet to review this area of research in a comprehensive, general manner. The current review therefore aims to highlight those anticancer polyphenols that target specific kinases in various types of cancer. The present review also provides an in-depth analysis of polyphenol structure-activity relationships in relation to their anticancer activities and specific kinase targeting. Lastly, a number of polyphenols are identified as potential antitumor agents that could be used to combat biologically aggressive cancers, including metastasizing cancers, through the targeting of specific kinases.
引用
收藏
页码:812 / 825
页数:14
相关论文
共 107 条
[91]   Effects of resveratrol on the autophosphorylation of phorbol ester-responsive protein kinases - Inhibition of protein kinase D but not protein kinase C isozyme autophosphorylation [J].
Stewart, JR ;
Christman, KL ;
O'Brian, CA .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (09) :1355-1359
[92]  
STOKER JR, 1962, J BIOL CHEM, V237, P2303
[93]   Effects of soy isoflavones on apoptosis induction and G2-M arrest in human hepatoma cells involvement of caspase-3 activation, Bcl-2 and BCI-XL downregulation, and Cdc2 kinase activity [J].
Su, SJ ;
Chow, NH ;
Kung, ML ;
Hung, TC ;
Chang, KL .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2003, 45 (01) :113-123
[94]   The effect of plant phenols on the expression and activity of phorbol ester-induced PKC in mouse epidermis [J].
Szaefer, Hanna ;
Kaczmarek, Jolanta ;
Rybczynska, Maria ;
Baer-Dubowska, Wanda .
TOXICOLOGY, 2007, 230 (01) :1-10
[95]   Green tea polyphenols and its constituent epigallocatechin gallate inhibits proliferation of human breast cancer cells in vitro and in vivo [J].
Thangapazham, Rajesh L. ;
Singh, Anoop K. ;
Sharma, Anuj ;
Warren, James ;
Gaddipati, Jaya P. ;
Maheshwari, Radha K. .
CANCER LETTERS, 2007, 245 (1-2) :232-241
[96]  
Virgili F., 1999, Research Communications in Biochemistry and Cell and Molecular Biology, V3, P95
[97]   Kinase inhibitors: Vice becomes virtue [J].
Vogt, Peter K. ;
Kang, Sohye .
CANCER CELL, 2006, 9 (05) :327-328
[98]   Black tea polyphenol theaflavins inhibit aromatase activity and attenuate tamoxifen resistance in HER2/neu-transfected human breast cancer cells through tyrosine kinase suppression [J].
Way, TD ;
Lee, HH ;
Kao, MC ;
Lin, JK .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (14) :2165-2174
[99]  
Weyant MJ, 2001, CANCER RES, V61, P118
[100]  
Wilson Mark A., 2008, BMC Pharmacology, V8, P15, DOI 10.1186/1471-2210-8-15