Relationship Between Plasma Estradiol Levels and Estrogen-Responsive Gene Expression in Estrogen Receptor-Positive Breast Cancer in Postmenopausal Women

被引:98
作者
Dunbier, Anita K. [1 ]
Anderson, Helen
Ghazoui, Zara
Folkerd, Elizabeth J.
A'Hern, Roger
Crowder, Robert J.
Hoog, Jeremy
Smith, Ian E.
Osin, Peter
Nerurkar, Ashutosh
Parker, Joel S.
Perou, Charles M.
Ellis, Matthew J.
Dowsett, Mitch
机构
[1] Royal Marsden Hosp, Acad Dept Biochem, Breakthrough Breast Canc Res Ctr, Inst Canc Res, London SW3 6JJ, England
基金
美国国家卫生研究院;
关键词
AROMATASE INHIBITOR; NEOADJUVANT ANASTROZOLE; PROGESTERONE-RECEPTOR; TAMOXIFEN; ALPHA; BETA; LETROZOLE; PROFILES; THERAPY; RISK;
D O I
10.1200/JCO.2009.23.9616
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine whether plasma estradiol (E2) levels are related to gene expression in estrogen receptor (ER)-positive breast cancers in postmenopausal women. Materials and Methods Genome-wide RNA profiles were obtained from pretreatment core-cut tumor biopsies from 104 postmenopausal patients with primary ER-positive breast cancer treated with neoadjuvant anastrozole. Pretreatment plasma E2 levels were determined by highly sensitive radioimmunoassay. Genes were identified for which expression was correlated with pretreatment plasma E2 levels. Validation was performed in an independent set of 73 ER-positive breast cancers. Results The expression of many known estrogen-responsive genes and gene sets was highly significantly associated with plasma E2 levels (eg, TFF1/pS2, GREB1, PDZK1 and PGR; P < .005). Plasma E2 explained 27% of the average expression of these four average estrogen-responsive genes (ie, AvERG; r = 0.51; P < .0001), and a standardized mean of plasma E2 levels and ER transcript levels explained 37% (r, 0.61). These observations were validated in an independent set of 73 ER-positive tumors. Exploratory analysis suggested that addition of the nuclear coregulators in a multivariable analysis with ER and E2 levels might additionally improve the relationship with the AvERG. Plasma E2 and the standardized mean of E2 and ER were both significantly correlated with 2-week Ki67, a surrogate marker of clinical outcome (r = -0.179; P = .05; and r = -0.389; P = .0005, respectively). Conclusion Plasma E2 levels are significantly associated with gene expression of ER-positive breast cancers and should be considered in future genomic studies of ER-positive breast cancer. The AvERG is a new experimental tool for the study of putative estrogenic stimuli of breast cancer. J Clin Oncol 28: 1161-1167. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:1161 / 1167
页数:7
相关论文
共 38 条
[1]   Predictors of response to aromatase inhibitors [J].
Anderson, Helen ;
Bulun, Serdar ;
Smith, Ian ;
Dowsett, Mitch .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2007, 106 (1-5) :49-54
[2]   Intratumoral aromatase model: The effects of letrozole (CGS 20267) [J].
Brodie, A ;
Lu, Q ;
Yue, W ;
Wang, JP ;
Liu, Y .
BREAST CANCER RESEARCH AND TREATMENT, 1998, 49 (Suppl 1) :S23-S26
[3]   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
[4]   Estrogen receptor alpha and beta expression in upper gastrointestinal tract with regulation of trefoil factor family 2 mRNA levels in ovariectomized rats [J].
CampbellThompson, ML .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (02) :478-483
[5]   Influence of estrogen plus progestin on breast, cancer and mammography in healthy postmenopausal women - The Women's Health Initiative Randomized trial [J].
Chlebowski, RT ;
Hendrix, SL ;
Langer, RD ;
Stefanick, ML ;
Gass, M ;
Lane, D ;
Rodabough, RJ ;
Gilligan, MA ;
Cyr, MG ;
Thomson, CA ;
Khandekar, J ;
Petrovitch, H ;
McTiernan, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 289 (24) :3243-3253
[6]   PIK3CA and PIK3CB Inhibition Produce Synthetic Lethality when Combined with Estrogen Deprivation in Estrogen Receptor-Positive Breast Cancer [J].
Crowder, Robert J. ;
Phommaly, Chanpheng ;
Tao, Yu ;
Hoog, Jeremy ;
Luo, Jingqin ;
Perou, Charles M. ;
Parker, Joel S. ;
Miller, Melinda A. ;
Huntsman, David G. ;
Lin, Li ;
Snider, Jacqueline ;
Davies, Sherri R. ;
Olson, John A., Jr. ;
Watson, Mark A. ;
Saporita, Anthony ;
Weber, Jason D. ;
Ellis, Matthew J. .
CANCER RESEARCH, 2009, 69 (09) :3955-3962
[7]  
Dorgan JF, 1997, CANCER EPIDEM BIOMAR, V6, P177
[8]  
Dorgan JF, 2002, JNCI-J NATL CANCER I, V94, P606
[9]  
DOWSETT M, 1987, CANCER RES, V47, P1957
[10]   Biomarker changes during neoadjuvant anastrozole, tamoxifen, or the combination: Influence of hormonal status and HER-2 in breast cancer - A study from the IMPACT trialists [J].
Dowsett, M ;
Ebbs, SR ;
Dixon, JM ;
Skene, A ;
Griffith, C ;
Boeddinghaus, I ;
Salter, J ;
Detre, S ;
Hills, M ;
Ashley, S ;
Francis, S ;
Walsh, G ;
Smith, IE .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2477-2492