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Updated: Sep 10, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Current Status and Advances in Anti-Androgen Therapy for Triple-Negative Breast Cancer
1The Second Clinical Medical School of Shandong University, Jinan, 250033, China.
Abstract:
The heterogeneity of triple-negative breast cancer (TNBC) has spurred the exploration of precision therapies based on molecular subtypes, with the androgen receptor (AR)-positive subtype emerging as a potential therapeutic target. The treatment of AR-positive TNBC relies primarily on androgen receptor antagonists, such as enobosarm, bicalutamide, and enzalutamide. To enhance efficacy, researchers are investigating combination therapies that integrate anti-androgen agents with chemotherapy, immunotherapy, or PARP inhibitors. Additionally, studies have revealed that the AR signaling pathway regulates the tumor microenvironment, and AR inhibition may potentiate the efficacy of immune checkpoint inhibitors. However, anti-AR therapies face significant limitations and challenges due to multifaceted factors, necessitating further resolution. With continued advancements, AR-targeted therapy holds promise as a critical component of personalized treatment strategies for TNBC.
Insights
Androgen receptor (AR)-positive triple-negative breast cancer (TNBC) shows promise for targeted therapy using AR antagonists. Combination treatments and understanding AR
Area of Science:
- Oncology
- Molecular Biology
- Precision Medicine
Background:
- Triple-negative breast cancer (TNBC) is heterogeneous, necessitating subtype-specific treatments.
- Androgen receptor (AR)-positive TNBC is a recognized molecular subtype with therapeutic potential.
- Current treatments for AR-positive TNBC primarily involve AR antagonists like enobosarm, bicalutamide, and enzalutamide.
Purpose of the Study:
- To explore the therapeutic potential of AR-targeted therapies in AR-positive TNBC.
- To investigate combination strategies to enhance the efficacy of anti-AR agents.
- To elucidate the role of AR signaling in the tumor microenvironment and its interaction with immunotherapy.
Main Methods:
- Review of existing literature on AR-targeted therapies in TNBC.
- Analysis of preclinical and clinical studies investigating AR antagonists.
- Exploration of combination therapy approaches including chemotherapy, immunotherapy, and PARP inhibitors.
Main Results:
- AR antagonists are primary agents for AR-positive TNBC.
- Combination therapies integrating anti-AR agents with chemotherapy, immunotherapy, or PARP inhibitors are under investigation.
- AR signaling influences the tumor microenvironment, suggesting AR inhibition can enhance immune checkpoint inhibitor efficacy.
Conclusions:
- AR-targeted therapy is a promising strategy for personalized treatment of AR-positive TNBC.
- Further research is needed to overcome limitations and challenges associated with anti-AR therapies.
- Combination approaches hold potential for improving treatment outcomes in TNBC.
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