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Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
Gene expression profiles in breast cancer to identify estrogen receptor target genes
1Disciplina de Oncologia, Departamento de Radiologia da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo, 455, 40 andar, CEP 01246-903, São Paulo, Brazil. nagai@usp.br
Abstract:
The estrogens play important role in the homeostatic maintenance of several target tissues including those in the mammary gland, uterus, bone, cardiovascular system, and brain. Most of estrogen's action is thought to be mediated through its nuclear estrogen receptors, ERalpha and ERbeta, which are members of the nuclear receptor superfamily that act as ligand-induced transcription factors. Acting via its receptors, estrogen also plays an essential role in the development and progression of human breast cancer. The ER and progesterone receptor (PR), which are regulated by estrogen via ER, have been used as prognostic markers in the clinical management of breast cancer patients. However, the prognosis of a patient with ER+/PR+ breast cancer can be highly variable and a significant proportion of hormone receptor positive breast cancers does not respond to endocrine therapy. The identification of estrogen receptor target genes may improve our understanding of the role played by estrogens in breast cancer making it possible to better tailor hormone treatments and improve a patient's response to hormonal therapy. In this review, we explore the literature for data regarding the identification of estrogen receptor-regulated genes in breast cancer cell lines and breast tumor biopsies using high throughput technologies such as serial analysis of gene expression (SAGE) and cDNA microarrays.
Insights
Estrogen receptors (ERs) are crucial in breast cancer development and hormone therapy response. Identifying ER-regulated genes can improve treatment strategies for hormone-dependent breast cancers.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Estrogens are vital for maintaining homeostasis in various tissues, including the mammary gland.
- Estrogen receptors (ERalpha and ERbeta) mediate most estrogen actions as ligand-induced transcription factors.
- Estrogen signaling is integral to human breast cancer development and progression.
Purpose of the Study:
- To review the identification of estrogen receptor-regulated genes in breast cancer.
- To enhance understanding of estrogen's role in breast cancer.
- To improve tailored hormone treatments and patient response.
Main Methods:
- Literature review of studies identifying estrogen receptor-regulated genes.
- Analysis of high-throughput technologies like serial analysis of gene expression (SAGE) and cDNA microarrays.
- Examination of data from breast cancer cell lines and tumor biopsies.
Main Results:
- Estrogen receptors (ERalpha and ERbeta) are key mediators of estrogen's effects.
- ER and progesterone receptor (PR) status are used as prognostic markers in breast cancer.
- A significant portion of ER+/PR+ breast cancers show variable prognosis and resistance to endocrine therapy.
Conclusions:
- Identifying estrogen receptor target genes is crucial for understanding breast cancer.
- This knowledge can lead to better-tailored hormone therapies.
- Improved understanding may enhance patient response to hormonal treatments for breast cancer.
