Intestinal epithelial cell accumulation of the cancer preventive polyphenol ellagic acid - extensive binding to protein and DNA

被引:153
作者
Whitley, AC
Stoner, GD
Darby, MV
Walle, T
机构
[1] Med Univ S Carolina, Dept Cell & Mol Pharmacol & Expt Therapeut, Charleston, SC 29425 USA
[2] Ohio State Univ, Sch Publ Hlth, Div Environm Hlth Sci, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[4] Ohio State Univ, Sch Publ Hlth, Coll Pharm, Columbus, OH 43210 USA
关键词
ellagic acid; irreversible binding; cellular uptake; Caco-2; cells; transport;
D O I
10.1016/S0006-2952(03)00413-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ellagic acid (EA), a polyphenol present in many berries, has been demonstrated to be preventive of esophageal cancer in animals both at the initiation and promotion stages. To be able to extrapolate these findings to humans we have studied the transcellular absorption and epithelial cell accumulation of [C-14]EA in the human intestinal Caco-2 cells. The apical (mucosal) to basolateral (serosal) transcellular transport of 10 muM [C-14]EA was minimal with a P-app of only 0.13 x 10(-6) cm/s, which is less than for the paracellular transport marker mannitol. In spite of observations of basolateral to apical efflux, Caco-2 cell uptake studies showed high accumulation of EA in the cells (1054 +/- 136 pmol/mg protein), indicating facile absorptive transport across the apical membrane. Surprisingly, as much as 93% of the cellular EA was irreversibly bound to macromolecules (982 +/- 151 pmol/mg protein). To confirm the irreversible nature of the binding to protein, Caco-2 cells treated with 10 muM [C-14]EA were subjected to SDS-PAGE analysis. This resulted in radiolabeled protein bands trapped in the stacking gel, consistent with [14C]EA-crosslinked proteins. Treatment of Caco-2 cells with 10 PM [14C]EA also revealed irreversible binding of EA to cellular DNA as much as five times higher than for protein (5020 +/- 773 pmol/mg DNA). Whereas the irreversible binding to protein required oxidation of EA by reactive oxygen species, this did not seem to be the case with the DNA binding. The avid irreversible binding to cellular DNA and protein may be the reason for its highly limited transcellular absorption. Thus, EA appears to accumulate selectively in the epithelial cells of the aerodigestive tract, where its cancer preventive actions may be displayed. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:907 / 915
页数:9
相关论文
共 38 条
[21]   Free radical studies of ellagic acid, a natural phenolic antioxidant [J].
Priyadarsini, KI ;
Khopde, SM ;
Kumar, SS ;
Mohan, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (07) :2200-2206
[22]   Risk factors for squamous cell carcinoma of the oesophagus [J].
Ribeiro, U ;
Posner, MC ;
SafatleRibeiro, AV ;
Reynolds, JC .
BRITISH JOURNAL OF SURGERY, 1996, 83 (09) :1174-1185
[23]   THE CRYSTAL AND MOLECULAR-STRUCTURE OF ELLAGIC ACID DIHYDRATE - A DIETARY ANTICANCER AGENT [J].
ROSSI, M ;
ERLEBACHER, J ;
ZACHARIAS, DE ;
CARRELL, HL ;
IANNUCCI, B .
CARCINOGENESIS, 1991, 12 (12) :2227-2232
[24]  
SAYER JM, 1983, J AM CHEM SOC, V1014, P5562
[25]   IRREVERSIBLE BINDING AND METABOLISM OF PROPRANOLOL BY HUMAN-LIVER MICROSOMES - RELATIONSHIP TO POLYMORPHIC OXIDATION [J].
SHAW, L ;
LENNARD, MS ;
TUCKER, GT ;
BAX, NDS ;
WOODS, HF .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (14) :2283-2288
[26]   DISPOSITION OF THE NATURALLY-OCCURRING ANTIMUTAGENIC PLANT PHENOL, ELLAGIC ACID, AND ITS SYNTHETIC DERIVATIVES, 3-O-DECYLELLAGIC ACID AND 3,3'-DI-O-METHYLELLAGIC ACID IN MICE [J].
SMART, RC ;
HUANG, MT ;
CHANG, RL ;
SAYER, JM ;
JERINA, DM ;
CONNEY, AH .
CARCINOGENESIS, 1986, 7 (10) :1663-1667
[27]  
Song SH, 1999, DRUG METAB DISPOS, V27, P689
[28]   Etiology and chemoprevention of esophageal squamous cell carcinoma [J].
Stoner, GD ;
Gupta, A .
CARCINOGENESIS, 2001, 22 (11) :1737-1746
[29]   Isothiocyanates and freeze-dried strawberries as inhibitors of esophageal cancer [J].
Stoner, GD ;
Kresty, LA ;
Carlton, PS ;
Siglin, JC ;
Morse, MA .
TOXICOLOGICAL SCIENCES, 1999, 52 (02) :95-100