Resveratrol reverses tumor-promoter-induced inhibition of gap-junctional intercellular communication

被引:64
作者
Nielsen, M
Ruch, RJ
Vang, O
机构
[1] Roskilde Univ, Dept Chem & Life Sci, DK-4000 Roskilde, Denmark
[2] Med Coll Ohio, Dept Pathol, Toledo, OH 43699 USA
关键词
resveratrol; gap-junctional intercellular communication; TPA; DDT; connexin; 43;
D O I
10.1006/bbrc.2000.3378
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
The naturally occurring stilbene/alexin trans-resveratrol (trans-3,5,4'-trihydroxystilbene) is a promising agent for the prevention of cancer. We investigated the effect of resveratrol on gap-junctional intercellular communication (GJIC) in WB-F344 rat liver epithelial cells because inhibition of GJIC is an important mechanism of tumor promotion. Seventeen to 50 mu M resveratrol increased GJIC significantly by a factor of 1.3 compared with solvent vehicle controls, when the WB-F344 cells were exposed to resveratrol for 6 h, Most; tumor promoters, including the phorbol ester TPA and the insecticide DDT, block GJIC, Resveratrol at 17-50 mu M also significantly prevented down-regulation of GJIC by TPA and DDT, by a factor of 2.7 and 1.8, respectively. This recovery of GJIC from TPA inhibition was partly correlated with hindered hyperphosphorylation of Cx43, In conclusion, resveratrol was found to enhance GJIC and counteract the effects of tumor promoters on GJIC, and this is likely a mechanism that contributes to the antipromotional and anticarcinogenic properties of resveratrol, (C) 2000 Academic Press.
引用
收藏
页码:804 / 809
页数:6
相关论文
共 27 条
[1]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[2]   Resveratrol arrests the cell division cycle at S/G2 phase transition [J].
Della Ragione, F ;
Cucciolla, V ;
Borriello, A ;
Della Pietra, V ;
Racioppi, L ;
Soldati, G ;
Manna, C ;
Galletti, P ;
Zappia, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (01) :53-58
[3]   SCRAPE-LOADING AND DYE TRANSFER - A RAPID AND SIMPLE TECHNIQUE TO STUDY GAP JUNCTIONAL INTERCELLULAR COMMUNICATION [J].
ELFOULY, MH ;
TROSKO, JE ;
CHANG, CC .
EXPERIMENTAL CELL RESEARCH, 1987, 168 (02) :422-430
[4]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[5]   The cancer chemopreventive agent resveratrol is incorporated into model membranes and inhibits protein kinase C α activity [J].
García-García, J ;
Micol, V ;
de Godos, A ;
Gómez-Fernández, JC .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1999, 372 (02) :382-388
[6]   Gap junction endocytosis and lysosomal degradation of connexin43-P2 in WB-F344 rat liver epithelial cells treated with DDT and lindane [J].
Guan, XJ ;
Ruch, RJ .
CARCINOGENESIS, 1996, 17 (09) :1791-1798
[7]   Recent advances in chemoprevention of cancer [J].
Hong, WK ;
Sporn, MB .
SCIENCE, 1997, 278 (5340) :1073-1077
[8]  
Hossain MZ, 1998, J CELL PHYSIOL, V176, P332, DOI 10.1002/(SICI)1097-4652(199808)176:2<332::AID-JCP11>3.3.CO
[9]  
2-O
[10]   REDOX-ACTIVE CHALCOGEN-CONTAINING GLUTATHIONE-PEROXIDASE MIMETICS AND ANTIOXIDANTS INHIBIT TUMOR PROMOTER-INDUCED DOWN-REGULATION OF GAP JUNCTIONAL INTERCELLULAR COMMUNICATION BETWEEN WB-F344 LIVER EPITHELIAL-CELLS [J].
HU, J ;
ENGMAN, L ;
COTGREAVE, IA .
CARCINOGENESIS, 1995, 16 (08) :1815-1824