Literature DB >> 19059610

GATA-3 as a marker of hormone response in breast cancer.

Sandy H Fang1, Yizhen Chen, Ronald J Weigel.   

Abstract

GATA-3 is a transcription factor that orchestrates gene expression profiles during embryogenesis of a variety of human tissues, including hematopoietic cells, skin, kidney, mammary gland, and the central nervous system. Among several other roles, GATA-3 has recently been identified as a key player of luminal cell differentiation in the mammary gland. The majority of breast cancers arise from luminal epithelial cells and hence GATA-3 appears to control a set of genes involved in the differentiation and proliferation of breast cancer. The expression of GATA-3 has a strong association with the expression of estrogen receptor-alpha (ER) in breast cancer, and there is mounting evidence that GATA-3 can be used as a clinical marker to determine response to hormonal therapy and to refine the prognosis of breast cancer patients. Here, we review the literature from the past 10 y on GATA-3 in normal and pathological states of the mammary gland. Conclusions from the literature are confirmed using meta-analyses performed by the Oncomine Research Platform.

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Year:  2008        PMID: 19059610     DOI: 10.1016/j.jss.2008.07.015

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  22 in total

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5.  Indole-3-carbinol triggers aryl hydrocarbon receptor-dependent estrogen receptor (ER)alpha protein degradation in breast cancer cells disrupting an ERalpha-GATA3 transcriptional cross-regulatory loop.

Authors:  Crystal N Marconett; Shyam N Sundar; Kevin M Poindexter; Theresa R Stueve; Leonard F Bjeldanes; Gary L Firestone
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Authors:  Ashley Cimino-Mathews; Andrea P Subhawong; Peter B Illei; Rajni Sharma; Marc K Halushka; Russell Vang; John H Fetting; Ben Ho Park; Pedram Argani
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7.  S100A8/A9 is associated with estrogen receptor loss in breast cancer.

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Review 10.  ER and PR signaling nodes during mammary gland development.

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Journal:  Breast Cancer Res       Date:  2012-07-19       Impact factor: 6.466

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