The Influence of Endocrine Disrupting Chemicals on the Proliferation of ERα Knockdown-Human Breast Cancer Cell Line MCF-7; New Attempts by RNAi Technology

被引:21
作者
Miyakoshi, Takashi [1 ]
Miyajima, Katsuhiro [1 ]
Takekoshi, Susumu [1 ]
Osamura, Robert Yoshiyuki [1 ]
机构
[1] Tokai Univ, Dept Pathol, Sch Med, Kanagawa 2591193, Japan
关键词
Bisphenol A (BPA); estrogen receptor alpha (ER alpha); RNA interference (RNAi); MCF-7; cell proliferation; ESTROGEN-RECEPTOR-ALPHA; BISPHENOL-A; PRENATAL EXPOSURE; IN-VITRO; XENOESTROGENS; MECHANISMS; COATINGS; ASSAY;
D O I
10.1267/ahc.08036
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bisphenol A (BPA) is a monomer use in manufacturing a wide range of chemical products which include epoxy resins and polycarbonate. It has been reported that BPA increases the cell proliferation activity of human breast cancer MCF-7 cells as well as 17-beta estradiol (E2) and diethylstilbestrol (DES). However, BPA induces target genes through ER-dependent and ER-independent manners which are different from the actions induced by E2. Therefore, BPA may be unique in estrogen-dependent cell proliferation compared to other endocrine disrupting chemicals (EDCs). In the present study, to test whether ER alpha is essential to the BPA-induced proliferation on MCF-7 cells, we suppressed the ER alpha expression of MCF-7 cells by RNA interference (RNAi). Proliferation effects in the presence of E2, DES and BPA were not observed in ER alpha-knockdown MCF-7 cells in comparison with control MCF-7. In addition, a marker of proliferative potential, MIB-1 labeling index (LI), showed no change in BPA-treated groups compared with vehicle-treated groups on ER alpha-knockdown MCF-7 cells. In conclusion, we demonstrated that ER alpha has a role in BPA-induced cell proliferation as well as E2 and DES. Moreover, this study indicated that the direct knockdown of ERa using RNAi serves as an additional tool to evaluate, in parallel with MCF-7 cell proliferation assay, for potential EDCs.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 32 条
[1]   Food contamination from epoxy resins and organosols used as can coatings: analysis by gradient NPLC [J].
Biedermann, M ;
Grob, K .
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 1998, 15 (05) :609-618
[2]  
BORNSTEIN J, 1988, Obstetrical and Gynecological Survey, V43, P15
[3]  
BROTONS JA, 1995, ENVIRON HEALTH PERSP, V103, P608, DOI 10.2307/3432439
[4]   Bisphenol A interacts with the estrogen receptor α in a distinct manner from estradiol [J].
Gould, JC ;
Leonard, LS ;
Maness, SC ;
Wagner, BL ;
Conner, K ;
Zacharewski, T ;
Safe, S ;
McDonnell, DP ;
Gaido, KW .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1998, 142 (1-2) :203-214
[5]  
Harris CA, 1997, ENVIRON HEALTH PERSP, V105, P802, DOI 10.2307/3433697
[6]   Differential interactions of bisphenol A and 17β-estradiol with estrogen receptor α (ERα) and ERβ [J].
Hiroi, H ;
Tsutsumi, O ;
Momoeda, M ;
Tatai, Y ;
Osuga, Y ;
Taketani, Y .
ENDOCRINE JOURNAL, 1999, 46 (06) :773-778
[7]  
Kim H S, 2001, J Toxicol Sci, V26, P111, DOI 10.2131/jts.26.111
[8]   BISPHENOL-A - AN ESTROGENIC SUBSTANCE IS RELEASED FROM POLYCARBONATE FLASKS DURING AUTOCLAVING [J].
KRISHNAN, AV ;
STATHIS, P ;
PERMUTH, SF ;
TOKES, L ;
FELDMAN, D .
ENDOCRINOLOGY, 1993, 132 (06) :2279-2286
[9]   The activity of bisphenol A depends on both the estrogen receptor subtype and the cell type [J].
Kurosawa, T ;
Hiroi, H ;
Tsutsumi, O ;
Ishikawa, T ;
Osuga, Y ;
Fujiwara, T ;
Inoue, S ;
Muramatsu, M ;
Momoeda, M ;
Taketani, Y .
ENDOCRINE JOURNAL, 2002, 49 (04) :465-471
[10]  
Matthews Jason, 2003, Mol Interv, V3, P281, DOI 10.1124/mi.3.5.281