Literature DB >> 23954741

Estrogen receptor beta in breast cancer.

Lars-Arne Haldosén1, Chunyan Zhao2, Karin Dahlman-Wright3.   

Abstract

Estrogen is essential for growth and development of the mammary glands and has been associated with the promotion and growth of breast cancer and in line with this, most human breast cancers are initially estrogen-dependent and undergo regression when deprived of their supporting hormone. Estrogen exerts many of its effects via two nuclear estrogen receptors (ERs), ERα and ERβ. The discovery of a second ER, ERβ, demanded a full re-evaluation of estrogen action in all target tissues and different estrogen associated diseases, including human breast cancer. However, despite over 15 years of research, the exact role, if any, of ERβ in human breast cancer remains elusive. The main challenges now are to develop highly selective anti-ERβ antibodies that are applied to large well characterized human breast cancer samples to validate their diagnostic potential and to explore ERβ-selective agonists in animal models of breast cancer to validate their therapeutic potential.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Breast cancer; Breast cancer marker; ERbeta isoforms; Estrogen receptor beta

Mesh:

Substances:

Year:  2013        PMID: 23954741     DOI: 10.1016/j.mce.2013.08.005

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  61 in total

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Authors:  John R Hawse; Jodi M Carter; Kirsten G M Aspros; Elizabeth S Bruinsma; Justin W Koepplin; Vivian Negron; Malayannan Subramaniam; James N Ingle; Karen L Rech; Matthew P Goetz
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Review 6.  The molecular, cellular and clinical consequences of targeting the estrogen receptor following estrogen deprivation therapy.

Authors:  Ping Fan; Philipp Y Maximov; Ramona F Curpan; Balkees Abderrahman; V Craig Jordan
Journal:  Mol Cell Endocrinol       Date:  2015-06-05       Impact factor: 4.102

7.  Membrane-initiated estradiol signaling of epithelial-mesenchymal transition-associated mechanisms through regulation of tight junctions in human breast cancer cells.

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9.  AP-1 Is a Key Regulator of Proinflammatory Cytokine TNFα-mediated Triple-negative Breast Cancer Progression.

Authors:  Yichun Qiao; Huan He; Philip Jonsson; Indranil Sinha; Chunyan Zhao; Karin Dahlman-Wright
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Journal:  Breast Cancer Res Treat       Date:  2014-07-10       Impact factor: 4.872

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