Published 2004 | Version v1
Journal article

Advances in estrogen receptor biology: prospects for improvements in targeted breast cancer therapy

  • 1. Division of Molecular and Cellular Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, and Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (United States)

Description

Estrogen receptor (ER) has a crucial role in normal breast development and is expressed in the most common breast cancer subtypes. Importantly, its expression is very highly predictive for response to endocrine therapy. Current endocrine therapies for ER-positive breast cancers target ER function at multiple levels. These include targeting the level of estrogen, blocking estrogen action at the ER, and decreasing ER levels. However, the ultimate effectiveness of therapy is limited by either intrinsic or acquired resistance. Identifying the factors and pathways responsible for sensitivity and resistance remains a challenge in improving the treatment of breast cancer. With a better understanding of coordinated action of ER, its coregulatory factors, and the influence of other intracellular signaling cascades, improvements in breast cancer therapy are emerging

Availability note (English)

Available from http://dx.doi.org/10.1186/bcr742; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC314456

Additional details

Publishing Information

Journal Title
Breast Cancer Research (Print)
Journal Volume
6
Journal Issue
1
Journal Page Range
p. 39-52
ISSN
1465-5411

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47028823
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
BIOLOGY; ESTROGENS; GROWTH FACTORS; MAMMARY GLANDS; NEOPLASMS; RECEPTORS; THERAPY
Descriptors DEC
BODY; DISEASES; GLANDS; HORMONES; MEDICINE; MEMBRANE PROTEINS; MITOGENS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; STEROID HORMONES

Optional Information

Copyright
Copyright (c) 2004 BioMed Central Ltd
Notes
PMCID: PMC314456; PUBLISHER-ID: bcr742; PMID: 14680484; OAI: oai:pubmedcentral.nih.gov:314456