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Series GSE6577 Query DataSets for GSE6577
Status Public on Apr 01, 2007
Title Estrogen receptor beta expression is associated with tamoxifen response in ER alpha-negative breast carcinoma
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Purpose: Endocrine therapies, such as tamoxifen are commonly given to most patients with estrogen receptor (ER) alpha-positive breast carcinoma but are not indicated for persons with ERalpha-negative cancer. The factors responsible for response to tamoxifen in 5-10% of patients with ERalpha-negative tumors are not clear. The aim of the present study was to elucidate the biology and role of the second ER, ERbeta, in patients treated with adjuvant tamoxifen.
Experimental Design: We investigated ERbeta by immunohistochemistry in 353 stage II primary breast tumors from patients treated with two years adjuvant tamoxifen, and generated gene expression profiles for a representative subset of 88 tumors.
Results: ERbeta was associated with increased survival (distant disease-free survival, P=0.01; overall survival, P=0.22), and in particular within ERalpha-negative patients (P=0.003; P=0.04), but not in the
ERalpha-positive subgroup (P=0.49; P=0.88). Lack of ERbeta conferred early relapse (hazard ratio, 14; 95% CI, 1.8-106; P=0.01) within the ERalpha-negative subgroup even after adjustment for other markers. ERalpha was an independent marker only within the ERbeta-negative tumors (hazard ratio, 0.44; 95% CI, 0.21-0.89; P=0.02). An ERbeta gene expression profile was identified and was markedly different from the ERalpha signature.
Conclusion: Expression of ERbeta is an independent marker for favorable prognosis after adjuvant tamoxifen treatment in ERalpha-negative breast cancer patients, and involves a gene expression program
distinct from ERalpha. These results may be highly clinically significant, because in the U.S. alone, approximately 10,000 women are diagnosed annually with ERalpha-negative/ERbeta-positive breast carcinoma and may benefit from adjuvant tamoxifen.
Keywords: Disease state analysis
 
Overall design 88 breast cancer tumor samples were analyzed on 2-color cDNA microarrays containing ~27K reporters with Stratagene Universal Human Reference RNA as the common reference sample.
 
Contributor(s) Gruvberger-Saal SK, Bendahl P, Saal LH, Laakso M, Hegardt C, Eden P, Peterson C, Malmstrom P, Isola J, Borg A, Ferno M
Citation(s) 17404078, 18559090
Submission date Dec 20, 2006
Last update date Jun 07, 2019
Contact name Sofia K Gruvberger-Saal
E-mail(s) sg2414@columbia.edu
Phone 212-851-5263
Organization name Columbia University
Department Institute for Cancer Genetics
Street address 1130 St. Nicholas Ave., ICRC 406
City New York
State/province NY
ZIP/Postal code 10032
Country USA
 
Platforms (1)
GPL3883 Swegene Human 27K RAP UniGene188 array
Samples (88)
GSM152028 C10109
GSM152029 C10289
GSM152030 C10335
Relations
BioProject PRJNA98759

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Supplementary file Size Download File type/resource
GSE6577_RAW.tar 218.6 Mb (http)(custom) TAR (of GPR)

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