Estrogenic and DNA-damaging activity of Red No 3 in human breast cancer cells

被引:35
作者
Dees, C
Askari, M
Garrett, S
Gehrs, K
Henley, D
Ardies, CM
机构
[1] OAK RIDGE NATL LAB, HLTH SCI RES DIV, OAK RIDGE, TN USA
[2] UNIV TENNESSEE, KNOXVILLE, TN USA
[3] OAK RIDGE INST SCI EDUC, OAK RIDGE, TN USA
[4] NE ILLINOIS UNIV, DEPT BIOL, CHICAGO, IL 60625 USA
关键词
xenoestrogen; red no 3; DDT; breast cancer; p53;
D O I
10.2307/3433381
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Exposure to pesticides, dyes, and pollutants that mimic the growth promoting effects of estrogen may cause breast cancer. The pesticide DDT and the food colorant Red No. 3 were found to increase the growth of HTB 133 but not estrogen receptor (ER) negative human breast cells (HTB 125) or rat liver epithelial cells (RLE). Red No. 3, beta-estradiol, and DDT increase ER site-specific DNA binding to the estrogen response element in HTB 133 cells and increase cyclin-dependent kinase 2 activity in MCF-7 breast cancer cells. Site-specific DNA binding by p53 in RLE, HTB 125, HTB 133, and MCF-7 cells was increased when they were treated with Red No. 3, which suggests that cellular DNA was damaged by this colorant. Red No. 3 increased binding of the ER from MCF-7 cells to the estrogen-responsive element. Consumption of Red No. 3, which has estrogenlike growth stimulatory properties and may be genotoxic, could be a significant risk factor in human breast carcinogenesis.
引用
收藏
页码:625 / 632
页数:8
相关论文
共 44 条
[1]   PHOSPHORYLATION OF THE RETINOBLASTOMA PROTEIN BY CDK2 [J].
AKIYAMA, T ;
OHUCHI, T ;
SUMIDA, S ;
MATSUMOTO, K ;
TOYOSHIMA, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :7900-7904
[2]  
ANDERSON LF, 1994, JNCI-J NATL CANCER I, V76, P76
[3]   RETRACTED: Synergistic activation of estrogen receptor with combinations of environmental chemicals (Retracted Article) [J].
Arnold, SF ;
Klotz, DM ;
Collins, BM ;
Vonier, PM ;
Guillette, LJ ;
McLachlan, JA .
SCIENCE, 1996, 272 (5267) :1489-1492
[4]   PHENOL RED IN TISSUE-CULTURE MEDIA IS A WEAK ESTROGEN - IMPLICATIONS CONCERNING THE STUDY OF ESTROGEN-RESPONSIVE CELLS IN CULTURE [J].
BERTHOIS, Y ;
KATZENELLENBOGEN, JA ;
KATZENELLENBOGEN, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2496-2500
[5]   Activation of the unliganded estrogen receptor by EGF involves the MAP kinase pathway and direct phosphorylation [J].
Bunone, G ;
Briand, PA ;
Miksicek, RJ ;
Picard, D .
EMBO JOURNAL, 1996, 15 (09) :2174-2183
[6]   MEDICAL HYPOTHESIS - XENOESTROGENS AS PREVENTABLE CAUSES OF BREAST-CANCER [J].
DAVIS, DL ;
BRADLOW, HL ;
WOLFF, M ;
WOODRUFF, T ;
HOEL, DG ;
ANTONCULVER, H .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 101 (05) :372-377
[7]   INCREASED P53 SITE-SPECIFIC DNA-BINDING IN CELLS PRODUCING MUTANT P53 [J].
DEES, C ;
TRAVIS, CC .
CANCER LETTERS, 1995, 96 (02) :225-231
[8]  
Dees C, 1997, MOL CARCINOGEN, V18, P107, DOI 10.1002/(SICI)1098-2744(199702)18:2<107::AID-MC6>3.0.CO
[9]  
2-D
[10]  
DESAILLY E, 1994, JNCI-J NATL CANCER I, V86, P232