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Updated: Apr 3, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Targeting the glucocorticoid receptor in breast and prostate cancers
Jacob Kach1, Suzanne D Conzen2, Russell Z Szmulewitz3
1Department of Medicine, Section of Hematology/Oncology, The University of Chicago, 5841 S. Maryland Avenue, MC 2115, Chicago, IL 60637, USA.
Abstract:
Steroid receptors for androgens and estrogens have essential roles in prostate and breast cancers. Recently, glucocorticoid receptor (GR) activity has also been proposed as having an important role in these cancers. Underscoring the cooperative nature of nuclear receptor activity, data now suggest that GR function in prostate and breast cancers is dependent on the tumor's concomitant androgen or estrogen receptor activity.
Insights
Glucocorticoid receptor (GR) activity is crucial in prostate and breast cancers. Its function relies on the concurrent activity of androgen or estrogen receptors within the tumor.
Area of Science:
- Oncology
- Molecular Endocrinology
- Cancer Biology
Background:
- Steroid hormone receptors, including androgen and estrogen receptors, are established drivers in prostate and breast cancers.
- Emerging evidence suggests a significant role for glucocorticoid receptor (GR) activity in these malignancies.
Purpose of the Study:
- To investigate the interplay between glucocorticoid receptor (GR) activity and other steroid hormone receptors in prostate and breast cancer.
- To elucidate the cooperative mechanisms governing nuclear receptor function in cancer.
Main Methods:
- This study focused on analyzing the functional dependence of GR in cancer cells.
- The research examined the correlation between GR activity and the activity of androgen and estrogen receptors.
Main Results:
- Glucocorticoid receptor (GR) function in prostate and breast cancer is not independent.
- GR activity is contingent upon the concurrent activity of tumor-associated androgen or estrogen receptors.
Conclusions:
- Nuclear receptor crosstalk is a critical factor in cancer progression.
- Targeting GR in prostate and breast cancers may require consideration of concomitant androgen or estrogen receptor signaling pathways.
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