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Updated: May 23, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Androgen action and metabolism in prostate cancer
Sean M Green1, Elahe A Mostaghel, Peter S Nelson
1Divisions of Human Biology, Fred Hutchinson Cancer Research Center, Seattle WA, United States.
Abstract:
The transcriptional programs regulated through the activity of the androgen receptor (AR) modulate normal prostate development and the maintenance of prostatic functions at maturity. AR signaling also controls key survival and growth functions operative in prostate cancer. Inhibiting the AR program remains the key target in the treatment of advanced prostate cancer, and suppressing AR also holds great potential for preventing the development or progression of early stage prostate cancer. In this review, we detail molecular mechanisms of AR activity, cellular components contributing to the maintenance of AR signaling despite AR-ligand suppression, and discuss treatment strategies designed to target components of resistance to AR-directed therapeutics.
Insights
Androgen receptor (AR) signaling is crucial for prostate function and cancer growth. Targeting AR resistance mechanisms offers new therapeutic strategies for advanced prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Urology
Background:
- Androgen receptor (AR) signaling regulates prostate development and function.
- AR activity is critical for prostate cancer survival and growth.
- AR inhibition is a primary treatment strategy for advanced prostate cancer.
Purpose of the Study:
- To review the molecular mechanisms of AR activity.
- To identify cellular components maintaining AR signaling despite suppression.
- To discuss therapeutic strategies targeting AR resistance.
Main Methods:
- Literature review of AR signaling pathways.
- Analysis of molecular mechanisms in prostate cancer.
- Discussion of current and emerging treatment strategies.
Main Results:
- AR regulates critical prostate functions and cancer progression.
- Specific cellular components sustain AR signaling even with AR-ligand suppression.
- Resistance to AR-directed therapies is a significant clinical challenge.
Conclusions:
- Understanding AR molecular mechanisms is key to prostate cancer treatment.
- Targeting AR signaling and resistance pathways is essential for therapeutic success.
- Further research into AR resistance is needed to improve patient outcomes.
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