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Estrogen Receptor (ESR1) mRNA Expression and Benefit From Tamoxifen in the Treatment and Prevention of Estrogen Receptor–Positive Breast Cancer
Author(s) -
Chungyeul Kim,
Gong Tang,
Katherine L. PogueGeile,
Joseph P. Costantino,
Frederick L. Baehner,
Joffre Baker,
Maureen Cronin,
Drew Watson,
Steven Shak,
Olga L. Bohn,
Debora Fumagalli,
Yusuke Taniyama,
Ahwon Lee,
Megan Reilly,
Victor G. Vogel,
Worta McCaskillStevens,
Leslie G. Ford,
Charles E. Geyer,
D. Lawrence Wickerham,
Norman Wolmark,
Soonmyung Paik
Publication year - 2011
Publication title -
journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.482
H-Index - 548
eISSN - 1527-7755
pISSN - 0732-183X
DOI - 10.1200/jco.2010.32.9615
Subject(s) - tamoxifen , breast cancer , estrogen receptor , medicine , estrogen receptor alpha , oncology , estrogen , cancer research , predictive marker , cancer
Several mechanisms have been proposed to explain tamoxifen resistance of estrogen receptor (ER) -positive tumors, but a clinically useful explanation for such resistance has not been described. Because the ER is the treatment target for tamoxifen, a linear association between ER expression levels and the degree of benefit from tamoxifen might be expected. However, such an association has never been demonstrated with conventional clinical ER assays, and the ER is currently used clinically as a dichotomous marker. We used gene expression profiling and ER protein assays to help elucidate molecular mechanism(s) responsible for tamoxifen resistance in breast tumors.

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