The expression and function of estrogen receptor α and β in human breast cancer and its clinical application

被引:146
作者
Hayashi, SI [1 ]
Eguchi, H [1 ]
Tanimoto, K [1 ]
Yoshida, T [1 ]
Omoto, Y [1 ]
Inoue, A [1 ]
Yosida, N [1 ]
Yamaguchi, Y [1 ]
机构
[1] Saitama Canc Ctr, Res Inst, Div Endocrinol, Ina, Saitama 362, Japan
关键词
D O I
10.1677/erc.0.0100193
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The overexpression of estrogen receptor alpha (ERalpha) is frequently observed in the early stage of breast cancer. We previously reported that the specific promoter of the ERalpha gene is responsible for this enhanced transcription of the gene, and identified the cis-acting elements which play an important role in its transcription. Furthermore, methylation of the ERalpha gene promoters also contribute to the regulation of gene transcription. Elucidation of these mechanisms of ERalpha gene expression may provide useful information for the early detection and chemoprevention of breast cancer. On the other hand, the expression of ERbeta has been reported in breast cancer. We have also assessed the significance and function of ERbeta and its variant types in breast cancer, and suggest that ERbeta and ERbetacx specifically suppress the function of ERalpha through different mechanisms. ERbeta isoforms may be important functional modulators of the estrogen-signaling pathway in breast cancer cells, and might affect the clinical outcome of patients. Moreover, to address the role of these ERs on the estrogen-dependent growth of breast cancer cells and to develop a diagnostic tool, we have analyzed the gene expression profiles of estrogen-responsive genes using cDNA microarray. Based on these results, the expression of several candidate genes in breast cancer tissues were analyzed by real-time RT-PCR and by immunohistochemical techniques, in order to discover new predictive factors for the endocrine therapy of patients with breast cancer. These studies could provide new clues for the elucidation of the estrogen-dependent mechanisms of cancer and the clinical benefits for patients.
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页码:193 / 202
页数:10
相关论文
共 22 条
[1]   CHARACTERIZATION OF THE PROXIMAL ESTROGEN-RESPONSIVE ELEMENT OF HUMAN CATHEPSIN-D GENE [J].
AUGEREAU, P ;
MIRALLES, F ;
CAVAILLES, V ;
GAUDELET, C ;
PARKER, M ;
ROCHEFORT, H .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (06) :693-703
[2]   ACTIVATION OF PS2 GENE-TRANSCRIPTION IS A PRIMARY RESPONSE TO ESTROGEN IN THE HUMAN-BREAST CANCER CELL-LINE MCF-7 [J].
BROWN, AMC ;
JELTSCH, JM ;
ROBERTS, M ;
CHAMBON, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (20) :6344-6348
[3]   RERG is a novel ras-related, estrogen-regulated and growth-inhibitory gene in breast cancer [J].
Finlin, BS ;
Gau, CL ;
Murphy, GA ;
Shao, HP ;
Kimel, T ;
Seitz, RS ;
Chiu, YF ;
Botstein, D ;
Brown, PO ;
Tamanoi, F ;
Andres, DA ;
Perou, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) :42259-42267
[4]  
Ghosh MG, 2000, CANCER RES, V60, P6367
[5]   Two promoters in expression of estrogen receptor messenger RNA in human breast cancer [J].
Hayashi, S ;
Imai, K ;
Suga, K ;
Kurihara, T ;
Higashi, Y ;
Nakachi, K .
CARCINOGENESIS, 1997, 18 (03) :459-464
[6]   Functional modulation of estrogen receptor by redox state with reference to thioredoxin as a mediator [J].
Hayashi, S ;
HajiroNakanishi, K ;
Makino, Y ;
Eguchi, H ;
Yodoi, J ;
Tanaka, H .
NUCLEIC ACIDS RESEARCH, 1997, 25 (20) :4035-4040
[7]  
Huynh H, 1996, CELL GROWTH DIFFER, V7, P1501
[8]   Development of cDNA microarray for expression profiling of estrogen-responsive genes [J].
Inoue, A ;
Yoshida, N ;
Omoto, Y ;
Oguchi, S ;
Yamori, T ;
Kiyama, R ;
Hayashi, S .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 29 (02) :175-192
[9]   Cloning of a novel estrogen receptor expressed in rat prostate and ovary [J].
Kuiper, GGJM ;
Enmark, E ;
PeltoHuikko, M ;
Nilsson, S ;
Gustafsson, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5925-5930
[10]  
Leygue E, 1999, CANCER RES, V59, P1175