Abstract
Steroid receptors are ligand-induced transcription factors that have broad functions among all living animal species, ranging from control of sex differences, body weight, stress responses, and many others. Their binding to coregulator proteins is regulated by corepressors and coactivators that interchange upon stimulation with a ligand. Coregulator proteins are an imperative and understudied aspect of steroid receptor signaling. Here, we discuss steroid receptor basics from protein domain structures that allow them to interact with coregulators and other proteins, their essential functions as transcription factors, and other elemental protein–protein interactions. We deliberate about the mechanisms that coregulators control in steroid receptor signaling, sex hormone signaling differences, sex hormone treatment in the opposite sex, and how these affect the coregulator and sex steroid receptor complexes. The steroid receptor-coregulator signaling mechanisms are essential built-in components of the mammalian DNA that mediate physiological and everyday functions. Targeting their crosstalk might be useful when imbalances lead to disease. We introduce novel technologies, such as the PamGene PamStation, which make investigating the heterogeneity of the steroid receptor–coregulator complexes and targeting their binding more feasible. This review provides an extensive understanding of steroid receptor-coregulator signaling and how these interactions are intrinsic to many physiological functions that may offer therapeutic advantages.
| Original language | English |
|---|---|
| Article number | 108363 |
| Journal | Journal of Biological Chemistry |
| Volume | 301 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Authors
Funding
Financial support and sponsorship: This work was supported by the National Institutes of Health (NIH) grants R01DK121797 (T.D.H.J.), R01DA058933 (C.G. & T.D.H.J.), F31HL170972 (Z.A.K.), and F31HL175979 (E.A.B.) and a fellowship award from the America Heart Association (AHA) for 25PRE1374495 (G.J.M.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or AHA.
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | R01DA058933, R01DK121797, F31HL175979, F31HL170972 |
| National Institutes of Health (NIH) | |
| American the American Heart Association | 25PRE1374495 |
| American the American Heart Association |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- PamGene
- addiction
- androgen receptor
- cancer
- estrogen receptor
- glucocorticoid receptor
- metabolism
- mineralocorticoid receptor
- nuclear receptors
- progesterone receptor
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology
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Dive into the research topics of 'Steroid receptors and coregulators: Dissemination of sex differences and emerging technologies'. Together they form a unique fingerprint.Projects
- 1 Finished
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Glucocorticoid Receptor beta and Prostate Cancer in African Americans
Hinds, T. (PI)
University of Kentucky UNITE Research Priority Area
2/1/23 → 1/31/24
Project: Research project
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