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Updated: Feb 22, 2026

Primary Culture of Rat Adrenocortical Cells and Assays of Steroidogenic Functions
Published on: March 12, 2019
Peripheral sensitivity to steroids revisited
Abstract:
Resistance to steroid hormones presents a serious problem with respect to their mass use in therapy. It may be caused genetically by mutation of genes involved in hormonal signaling, not only steroid receptors, but also other players in the signaling cascade as co-regulators and other nuclear factors, mediating the hormone-born signal. Another possibility is acquired resistance which may develop under long-term steroid treatment, of which a particular case is down regulation of the receptors. In the review recent knowledge is summarized on the mechanism of main steroid hormone action, pointing to already proven or potential sites causing steroid resistance. We have attempted to address following questions: 1) What does stay behind differences among patients as to their response to the (anti)steroid treatment? 2) Why do various tissues/cells respond differently to the same steroid hormone though they contain the same receptors? 3) Are such differences genetically dependent? The main attention was devoted to glucocorticoids as the most frequently used steroid therapeutics. Further, androgen insensitivity is discussed with a particular attention to acquired resistance to androgen deprivation therapy of prostate cancer. Finally the potential causes are outlined of breast and related cancer(s) resistance to antiestrogen therapy.
Insights
Steroid hormone resistance, often genetic or acquired, impacts therapy effectiveness. Understanding mechanisms of steroid action and resistance is crucial for improving patient treatment outcomes.
Area of Science:
- Endocrinology
- Molecular Biology
- Pharmacology
Background:
- Steroid hormone therapies are widely used but frequently encounter resistance.
- Resistance can stem from genetic mutations or acquired changes in signaling pathways.
- Understanding resistance mechanisms is vital for optimizing therapeutic efficacy.
Purpose of the Study:
- To review current knowledge on steroid hormone action mechanisms.
- To identify key sites contributing to steroid resistance.
- To address patient variability, tissue-specific responses, and genetic influences on steroid resistance.
Main Methods:
- Comprehensive literature review of steroid hormone signaling.
- Analysis of genetic and acquired mechanisms of resistance.
- Focus on glucocorticoids, androgens, and antiestrogens.
Main Results:
- Steroid resistance arises from alterations in receptors, co-regulators, and nuclear factors.
- Glucocorticoid resistance mechanisms are detailed, alongside androgen insensitivity in prostate cancer.
- Potential causes of resistance to antiestrogen therapy in breast cancer are outlined.
Conclusions:
- Varied patient responses to steroid therapy are linked to genetic and acquired resistance factors.
- Tissue-specific responses and genetic dependencies influence therapeutic outcomes.
- Targeting identified resistance mechanisms may improve steroid-based treatments.
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