Gene expression, cell cycle arrest and MAPK signalling regulation in Caco-2 cells exposed to ellagic acid and its metabolites, urolithins

被引:140
作者
Gonzalez-Sarrias, Antonio [1 ]
Espin, Juan-Carlos [1 ]
Tomas-Barberan, Francisco A. [1 ]
Garcia-Conesa, Maria-Teresa [1 ]
机构
[1] CSIC, CEBAS, Dept Food Sci & Technol, Res Grp Qual Safety & Bioact Plant Foods, Murcia, Spain
关键词
Colon cancer; Ellagic acid; Gene expression; G2; M arrest; Urolithins; COLON-CANCER; APOPTOSIS; PATHWAYS; CHEMOPREVENTION; ANTIOXIDANT; POLYPHENOLS; PUNICALAGIN; PROTEIN; ERK; IDENTIFICATION;
D O I
10.1002/mnfr.200800150
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Novel gene expression profiles and cellular functions modulated in Caco-2 cells in response to the dietary polyphenol, ellagic acid (EA), and its colonic metabolites, urolithin-A (3,8-dihydroxy-6H-dibenzo[b,d] pyran-6-one) and urolithin-B (3-hydroxy-6H-dibenzo[b,d] pyran-6-one) have been identified. Exposure of cells to EA and urolithins arrested cell growth at the S- and G(2)/M-phases. Transcriptional profiling using microarray and functional analysis revealed changes in the expression levels of MAPK signalling genes such as, growth factor receptors (FGFR2, EGFR), oncogenes (K-Ras, c-My-c), and tumour suppressors (DUSP6, Fos) and of genes involved in cell cycle (CCNBI, CCNBIIPI). Results suggest that EA and urolithin-A and -B, at concentrations achievable in the lumen from the diet, might contribute to colon cancer prevention by modulating the expression of multiple genes in epithelial cells lining the colon. Some of these genes are involved in key cellular processes associated with cancer development and are currently being investigated as potential chemopreventive targets.
引用
收藏
页码:686 / 698
页数:13
相关论文
共 53 条
[1]   Carcinogenic food contaminants [J].
Abnet, Christian C. .
CANCER INVESTIGATION, 2007, 25 (03) :189-196
[2]   BABELOMICS: a suite of web tools for functional annotation and analysis of groups of genes in high-throughput experiments [J].
Al-Shahrour, F ;
Minguez, P ;
Vaquerizas, JM ;
Conde, L ;
Dopazo, J .
NUCLEIC ACIDS RESEARCH, 2005, 33 :W460-W464
[3]   Taxol-induced apoptosis depends on MAP kinase pathways (ERK and p38) and is independent of p53 [J].
Bacus, SS ;
Gudkov, AV ;
Lowe, M ;
Lyass, L ;
Yung, Y ;
Komarov, AP ;
Keyomarsi, K ;
Yarden, Y ;
Seger, R .
ONCOGENE, 2001, 20 (02) :147-155
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]  
BERMUDEZSOTO MJ, 2007, J NUTR BIOCH, V4, P259
[6]   Catalytic activation of the phosphatase MKP-3 by ERK2 mitogen-activated protein kinase [J].
Camps, M ;
Nichols, A ;
Gillieron, C ;
Antonsson, B ;
Muda, M ;
Chabert, C ;
Boschert, U ;
Arkinstall, S .
SCIENCE, 1998, 280 (5367) :1262-1265
[7]   Expression and genomic profiling of colorectal cancer [J].
Cardoso, J. ;
Boer, J. ;
Morreau, H. ;
Fodde, R. .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2007, 1775 (01) :103-137
[8]  
Castonguay A, 1997, INT J ONCOL, V10, P367
[9]   Identification of urolithin A as a metabolite produced by human colon microflora from ellagic acid and related compounds [J].
Cerdá, B ;
Periago, P ;
Espín, JC ;
Tomás-Barberán, FA .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (14) :5571-5576
[10]   Metabolism of antioxidant and chemopreventive ellagitannins from strawberries, raspberries, walnuts, and oak-aged wine in humans:: Identification of biomarkers and individual variability [J].
Cerdá, B ;
Tomás-Barberán, FA ;
Espín, JC .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (02) :227-235