Estrogen receptor alpha in human breast cancer: Occurrence and significance

被引:249
作者
Ali, S [1 ]
Coombes, RC [1 ]
机构
[1] Hammersmith Hosp, Imperial Coll, Sch Med, Dept Canc Med,CRC Labs, MRC Cyclotron Bldg,Du Cane Rd, London W12 0NN, England
关键词
breast cancer; estrogen receptor; endocrine therapies; resistance;
D O I
10.1023/A:1009594727358
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Estrogens have long been recognized as being important for stimulating the growth of a large proportion of breast cancers. Now it is recognized that estrogen action is mediated by two receptors, and the presence of estrogen receptor alpha (ER alpha)(3) correlates with better prognosis and the likelihood of response to hormonal therapy. Over half of all breast cancers overexpress ER alpha and around 70% of these respond to anti-estrogen (for example tamoxifen) therapy. In addition, the presence of elevated levels of ER alpha in benign breast epithelium appears to indicate an increased risk of breast cancer, suggesting a role for ER alpha in breast cancer initiation, as well as progression. However, a proportion of ER alpha -positive tumors does not respond to endocrine therapy and the majority of those that do respond eventually become resistant. Most resistant tumors remain ER alpha -positive and frequently respond to alternative endocrine treatment, indicative of a continued role for ER alpha in breast cancer cell proliferation. The problem of resistance has resulted in the search for and the development of diverse hormonal therapies designed to inhibit ER alpha action, while research on the mechanisms which underlie resistance has shed light on the cellular mechanisms, other than ligand binding, which control ER alpha function.
引用
收藏
页码:271 / 281
页数:11
相关论文
共 86 条
[61]  
RICKETTS D, 1991, CANCER RES, V51, P1817
[62]   Oestrogen receptor: A stable phenotype in breast cancer [J].
Robertson, JFR .
BRITISH JOURNAL OF CANCER, 1996, 73 (01) :5-12
[63]   Potentiation of human estrogen receptor α transcriptional activation through phosphorylation of serines 104 and 106 by the cyclin A-CDK2 complex [J].
Rogatsky, I ;
Trowbridge, JM ;
Garabedian, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (32) :22296-22302
[64]   Role of hormones in mammary cancer initiation and progression [J].
Russo, IH ;
Russo, J .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 1998, 3 (01) :49-61
[65]  
SADOVSKY Y, 1995, MOL CELL BIOL, V15, P1554
[66]  
SAJI S, 2000, MED SCI, V97, P337
[67]   THE CRYSTAL-STRUCTURE OF THE ESTROGEN-RECEPTOR DNA-BINDING DOMAIN BOUND TO DNA - HOW RECEPTORS DISCRIMINATE BETWEEN THEIR RESPONSE ELEMENTS [J].
SCHWABE, JWR ;
CHAPMAN, L ;
FINCH, JT ;
RHODES, D .
CELL, 1993, 75 (03) :567-578
[68]   Modulating nuclear receptor function: may the phos be with you [J].
Shao, DL ;
Lazar, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (12) :1617-1618
[69]   The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen [J].
Shiau, AK ;
Barstad, D ;
Loria, PM ;
Cheng, L ;
Kushner, PJ ;
Agard, DA ;
Greene, GL .
CELL, 1998, 95 (07) :927-937
[70]   Hyperexpression of mitogen-activated protein kinase in human breast cancer [J].
Sivaraman, VS ;
Wang, HY ;
Nuovo, GJ ;
Malbon, CC .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1478-1483