Estrogen regulation of c-fos gene expression through phosphatidylinositol-3-kinase-dependent activation of serum response factor in MCF-7 breast cancer cells

被引:69
作者
Duan, RQ [1 ]
Xie, W [1 ]
Li, XR [1 ]
McDougal, A [1 ]
Safe, S [1 ]
机构
[1] Texas A&M Univ, Dept Vet Physiol & Pharmacol, College Stn, TX 77843 USA
关键词
P13-K estrogen; ER alpha; c-fos; SRF;
D O I
10.1016/S0006-291X(02)00499-0
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
17beta-Estradiol (E2) induces proliferation and c-fos gene expression in MCF-7 cells and both responses are partially blocked by wortmannin and LY294002 which are inhibitors of phosphatidylinositol-3-kinase (M-K). Analysis of the c-os gene promoter shows that the effects of wortmannin and LY294002 are associated with inhibition of E2-induced activation through the serum response factor (SRF) motif within the proximal serum response element at -325 and -296. E2 activates constructs containing multiple copies of the SRF (pSRF) and a GAL4-SRF fusion proteins these responses are accompanied by PI3-K-dependent phosphorylation of Akt and inhibited by wortmannin/LY294002, the antiestrogen ICI 182780, but not by the mitogen-activated protein kinase kinase (,MAPKK) inhibitor PD98059. Using a series of kinase inhibitors and dominant negative kinase expression plasmids, it was shown that the non-genomic activation of SRF by E2 was associated with src-ras-PI3-K pathway, thus, demonstrating hormonal activation of the SRE through src-ras activation of both PI3-K- and MAPK-dependent signaling pathways. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:384 / 394
页数:11
相关论文
共 50 条
[1]   Calmodulin is essential for estrogen receptor interaction with its motif and activation of responsive promoter [J].
Biswas, DK ;
Reddy, PV ;
Pickard, M ;
Makkad, B ;
Pettit, N ;
Pardee, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (50) :33817-33824
[2]  
Bonapace IM, 1996, ONCOGENE, V12, P753
[3]   Phosphatidylinositol 3-kinase/AKT-mediated activation of estrogen receptor α -: A new model for anti-estrogen resistance [J].
Campbell, RA ;
Bhat-Nakshatri, P ;
Patel, NM ;
Constantinidou, D ;
Ali, S ;
Nakshatri, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9817-9824
[4]   PI3-kinase in concert with Src promotes the S-phase entry of oestradiol-stimulated MCF-7 cells [J].
Castoria, G ;
Migliaccio, A ;
Bilancio, A ;
Di Domenico, M ;
de Falco, A ;
Lombardi, M ;
Fiorentino, R ;
Varricchio, L ;
Barone, MV ;
Auricchio, F .
EMBO JOURNAL, 2001, 20 (21) :6050-6059
[5]   Non-transcriptional action of oestradiol and progestin triggers DNA synthesis [J].
Castoria, G ;
Barone, MV ;
Di Domenico, M ;
Bilancio, A ;
Ametrano, D ;
Migliaccio, A ;
Auricchio, F .
EMBO JOURNAL, 1999, 18 (09) :2500-2510
[6]  
Curran T, 1988, ONCOGENE HDB, P307
[7]  
Darnell JE, 1996, RECENT PROG HORM RES, V51, P391
[8]   GROWTH-FACTORS IN BREAST-CANCER [J].
DICKSON, RB ;
LIPPMAN, ME .
ENDOCRINE REVIEWS, 1995, 16 (05) :559-589
[9]  
DICKSON RB, 1988, BREAST CANCER CELLUL, P119
[10]   UNREGULATED EXPRESSION OF C-JUN OR C-FOS PROTEINS BUT NOT JUN-D INHIBITS ESTROGEN-RECEPTOR ACTIVITY IN HUMAN BREAST-CANCER DERIVED CELLS [J].
DOUCAS, V ;
SPYROU, G ;
YANIV, M .
EMBO JOURNAL, 1991, 10 (08) :2237-2245