Regulation of estrogen receptor α function in breast cancer

被引:36
作者
Ferguson, AT [1 ]
Davidson, NE [1 ]
机构
[1] Johns Hopkins Oncol Ctr, Baltimore, MD 21231 USA
来源
CRITICAL REVIEWS IN ONCOGENESIS | 1997年 / 8卷 / 01期
关键词
mutation; transcription; methylation; alternative splicing; phosphorylation; coactivators;
D O I
10.1615/CritRevOncog.v8.i1.20
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
Estrogen receptor a (ER) plays a key role in the development and progression of breast cancer as well as the treatment and outcome of breast cancer patients. In normal mammary epithelial cells, the level of ER fluctuates during the menstrual cycle in response to cyclical changes in estrogen. However, in breast cancer normal control of ER gene expression and/or function is lost. Of particular interest, the absence of ER in mammary carcinomas is associated with a less-differentiated phenotype and resistance to endocrine therapies. This review focuses on our current understanding of the mechanisms that regulate ER a gene expression and function in breast cancer. These include alteration of the ER gene, loss of gene expression, alternative splicing of ER RNA, posttranslational modification of the protein, and interaction of ER with other proteins that can modify its function.
引用
收藏
页码:29 / 46
页数:18
相关论文
共 111 条
[1]   STEROID-RECEPTOR MEDIATED INHIBITION OF RAT PROLACTIN GENE-EXPRESSION DOES NOT REQUIRE THE RECEPTOR DNA-BINDING DOMAIN [J].
ADLER, S ;
WATERMAN, ML ;
XI, H ;
ROSENFELD, MG .
CELL, 1988, 52 (05) :685-695
[2]   MODULATION OF TRANSCRIPTIONAL ACTIVATION BY LIGAND-DEPENDENT PHOSPHORYLATION OF THE HUMAN ESTROGEN RECEPTOR-A/B REGION [J].
ALI, S ;
METZGER, D ;
BORNERT, JM ;
CHAMBON, P .
EMBO JOURNAL, 1993, 12 (03) :1153-1160
[3]  
Altucci L, 1996, ONCOGENE, V12, P2315
[4]  
ALVAREZ E, 1988, CANCER RES, V40, P277
[5]   HIGH-LEVELS OF DENOVO METHYLATION AND ALTERED CHROMATIN STRUCTURE AT CPG ISLANDS IN CELL-LINES [J].
ANTEQUERA, F ;
BOYES, J ;
BIRD, A .
CELL, 1990, 62 (03) :503-514
[6]   AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer [J].
Anzick, SL ;
Kononen, J ;
Walker, RL ;
Azorsa, DO ;
Tanner, MM ;
Guan, XY ;
Sauter, G ;
Kallioniemi, OP ;
Trent, JM ;
Meltzer, PS .
SCIENCE, 1997, 277 (5328) :965-968
[7]   Estradiol-binding mechanism and binding capacity of the human estrogen receptor is regulated by tyrosine phosphorylation [J].
Arnold, SF ;
Melamed, M ;
Vorojeikina, DP ;
Notides, AC ;
Sasson, S .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (01) :48-53
[8]   AN ANTIESTROGEN - A PHOSPHOTYROSYL PEPTIDE THAT BLOCKS DIMERIZATION OF THE HUMAN ESTROGEN-RECEPTOR [J].
ARNOLD, SF ;
NOTIDES, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7475-7479
[9]   ENHANCEMENT OF HUMAN ESTROGEN-RECEPTOR ACTIVITY BY SPT6 - A POTENTIAL COACTIVATOR [J].
BANIAHMAD, C ;
NAWAZ, Z ;
BANIAHMAD, A ;
GLEESON, MAG ;
TSAI, MJ ;
OMALLEY, BW .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (01) :34-43
[10]   EXPRESSION OF TRANSFORMING GROWTH FACTOR-ALPHA AND ITS MESSENGER RIBONUCLEIC-ACID IN HUMAN-BREAST CANCER - ITS REGULATION BY ESTROGEN AND ITS POSSIBLE FUNCTIONAL-SIGNIFICANCE [J].
BATES, SE ;
DAVIDSON, NE ;
VALVERIUS, EM ;
FRETER, CE ;
DICKSON, RB ;
TAM, JP ;
KUDLOW, JE ;
LIPPMAN, ME ;
SALOMON, DS .
MOLECULAR ENDOCRINOLOGY, 1988, 2 (06) :543-555