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Updated: May 4, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Androgen receptor signaling in prostate cancer
Zoran Culig1, Frédéric R Santer
1Division of Experimental Urology, Department of Urology, Innsbruck Medical University, Anichstrasse 35, 6020, Innsbruck, Austria, zoran.culig@i-med.ac.at.
Abstract:
The androgen receptor (AR), ligand-induced transcription factor, is expressed in primary prostate cancer and in metastases. AR regulates multiple cellular events, proliferation, apoptosis, migration, invasion, and differentiation. Its expression in prostate cancer cells is regulated by steroid and peptide hormones. AR downregulation by various compounds which are contained in fruits and vegetables is considered a chemopreventive strategy for prostate cancer. There is a bidirectional interaction between the AR and micro-RNA (miRNA) in prostate cancer; androgens may upregulate or downregulate the selected miRNA, whereas the AR itself is a target of miRNA. AR mutations have been discovered in prostate cancer, and their incidence may increase with tumor progression. AR mutations and increased expression of selected coactivators contribute to the acquisition of agonistic properties of anti-androgens. Expression of some of the coactivators is enhanced during androgen ablation. AR activity is regulated by peptides such as cytokines or growth factors which reduce the concentration of androgen required for maximal stimulation of the receptor. In prostate cancer, variant ARs which exhibit constitutive activity were detected. Novel therapies which interfere with intracrine synthesis of androgens or inhibit nuclear translocation of the AR have been introduced in the clinic.
Insights
The androgen receptor (AR) plays a key role in prostate cancer progression and is a target for novel therapies. Understanding AR regulation and mutations is crucial for developing effective chemopreventive and therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Endocrinology
Background:
- The androgen receptor (AR) is a ligand-induced transcription factor crucial for prostate cancer development and progression.
- AR regulates key cellular processes including proliferation, apoptosis, migration, invasion, and differentiation.
- AR expression is influenced by hormones and interacts bidirectionally with microRNAs (miRNAs).
Purpose of the Study:
- To review the multifaceted roles of the androgen receptor (AR) in prostate cancer.
- To explore AR regulation, mutations, and interactions with miRNAs and coactivators.
- To discuss current and emerging therapeutic strategies targeting the AR pathway.
Main Methods:
- Literature review of studies on androgen receptor function, regulation, and therapeutic targeting in prostate cancer.
- Analysis of AR interactions with hormones, miRNAs, and coactivators.
- Examination of AR mutations and their clinical implications.
Main Results:
- AR is central to prostate cancer, with its expression and activity modulated by hormones, peptides, and miRNAs.
- AR mutations and coactivator expression influence treatment response and disease progression.
- Novel therapies targeting AR signaling, including intracrine androgen synthesis and nuclear translocation, are emerging.
Conclusions:
- The androgen receptor (AR) is a critical therapeutic target in prostate cancer.
- Understanding the complex regulatory network of AR, including its interactions with miRNAs and coactivators, is vital for advancing treatment strategies.
- Emerging therapies offer new hope for managing advanced prostate cancer by directly interfering with AR signaling pathways.
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