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Updated: Mar 22, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Role of the androgen receptor in triple-negative breast cancer
Murtuza Rampurwala1, Kari B Wisinski1, Ruth O'Regan1
1University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Abstract:
Triple-negative breast cancer (TNBC) is an aggressive disease with outcomes inferior to those of other breast cancer subtypes. No targeted therapies are currently approved for TNBC, and newer treatment approaches are critically needed. It is increasingly recognized that TNBC is a heterogeneous disease, and the role of androgen signaling in a subset of TNBC is emerging. Although the degree of androgen receptor (AR) expression in TNBC varies widely depending on the assay methodology, cutoff for positivity, and patient population, existing evidence suggests an association between a higher level of AR expression and improved outcomes. Despite lower pathologic complete response (pCR) rates with neoadjuvant therapy, patients with AR-dependent TNBCs have a better prognosis than those with TNBCs that are not AR-dependent. Furthermore, gene expression profiling has been used to identify a luminal androgen receptor subtype of TNBC that is dependent on AR signaling. Early clinical studies investigating agents targeting AR in advanced TNBC have produced promising results. We review herein the literature on the biology of AR in breast cancer and its prognostic and predictive role in TNBC, and we describe the results of early clinical trials with antiandrogens in this population. We also present our vision of the future development of newer therapeutic strategies in AR-dependent TNBC.
Insights
Androgen receptor (AR) signaling plays a key role in a subset of triple-negative breast cancer (TNBC). Targeting AR in AR-dependent TNBC shows promise for improved outcomes in this aggressive disease.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype with poor prognosis.
- Limited targeted therapies exist for TNBC, necessitating novel treatment strategies.
- Androgen receptor (AR) signaling is increasingly recognized in a subset of TNBC.
Purpose of the Study:
- To review the biology of AR in breast cancer.
- To examine the prognostic and predictive role of AR in TNBC.
- To summarize early clinical trial results of antiandrogen therapies in advanced TNBC.
Main Methods:
- Literature review of AR biology and its role in TNBC.
- Analysis of gene expression profiling data identifying AR-dependent subtypes.
- Summary of outcomes from early-phase clinical trials of antiandrogen agents.
Main Results:
- AR expression levels vary in TNBC, but higher expression correlates with improved outcomes.
- AR-dependent TNBCs show a better prognosis than non-AR-dependent TNBCs.
- Early clinical trials of antiandrogen therapies in advanced TNBC have yielded promising results.
Conclusions:
- AR signaling is a viable therapeutic target in a subset of TNBC.
- Targeting AR may offer a new treatment avenue for patients with AR-dependent TNBC.
- Further research and clinical development of antiandrogen strategies are warranted for AR-dependent TNBC.
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