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Updated: Oct 17, 2025

Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer
Published on: March 17, 2016
Steroid Receptors in Breast Cancer: Understanding of Molecular Function as a Basis for Effective Therapy Development
Wojciech Kowalczyk1, Grzegorz Waliszczak1, Robert Jach2
1Chair of Medical Biochemistry, Jagiellonian University Medical College, 7 Kopernika St., 31-034 Kraków, Poland.
Abstract:
Breast cancer remains one of the most important health problems worldwide. The family of steroid receptors (SRs), which comprise estrogen (ER), progesterone (PR), androgen (AR), glucocorticoid (GR) and mineralocorticoid (MR) receptors, along with a receptor for a secosteroid-vitamin D, play a crucial role in the pathogenesis of the disease. They function predominantly as nuclear receptors to regulate gene expression, however, their full spectrum of action reaches far beyond this basic mechanism. SRs are involved in a vast variety of interactions with other proteins, including extensive crosstalk with each other. How they affect the biology of a breast cell depends on such factors as post-translational modifications, expression of coregulators, or which SR isoform is predominantly synthesized in a given cellular context. Although ER has been successfully utilized as a breast cancer therapy target for years, research on therapeutic application of other SRs is still ongoing. Designing effective hormone therapies requires thorough understanding of the molecular function of the SRs. Over the past decades, huge amount of data was obtained in multiple studies exploring this field, therefore in this review we attempt to summarize the current knowledge in a comprehensive way.
Insights
Steroid receptors (SRs) are crucial in breast cancer pathogenesis. Understanding their complex interactions and functions is key to developing new hormone therapies beyond estrogen receptor targeting.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Breast cancer is a major global health issue.
- Steroid receptors (SRs), including estrogen (ER), progesterone (PR), and androgen (AR) receptors, are implicated in breast cancer development.
- Their functions extend beyond gene regulation, involving protein interactions and crosstalk.
Purpose of the Study:
- To comprehensively review current knowledge on the role of SRs in breast cancer.
- To summarize the molecular functions of SRs for improved therapeutic strategies.
- To highlight ongoing research into the therapeutic applications of various SRs.
Main Methods:
- Literature review of studies on steroid receptors and breast cancer.
- Analysis of data on SRs' interactions, post-translational modifications, and coregulator expression.
- Synthesis of information on SR isoforms and their cellular context.
Main Results:
- SRs play a critical role in breast cancer pathogenesis through complex mechanisms.
- ER is a validated therapeutic target, but research on other SRs is expanding.
- Factors like post-translational modifications and coregulator expression influence SR function.
Conclusions:
- A thorough understanding of SR molecular functions is essential for designing effective hormone therapies.
- Further research into non-ER SRs holds promise for novel breast cancer treatments.
- This review consolidates existing knowledge to guide future therapeutic development.
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