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Updated: May 18, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Androgen receptor in triple negative breast cancer
K M McNamara1, T Yoda, K Takagi
1Department of Anatomical Pathology, Tohoku University School of Graduate Medicine, Japan. kmcnamara@patholo2.med.tohoku.ac.jp
Triple negative breast cancer (TNBC) management is difficult. Androgen receptor (AR) presence in TNBC cells offers potential therapeutic targets, but its role remains unclear, necessitating further research.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) presents significant clinical challenges due to its aggressive nature and limited targeted therapies.
- A subset of TNBC cases expresses the androgen receptor (AR), suggesting potential therapeutic avenues through androgen signaling manipulation or AR-targeted treatments.
Purpose of the Study:
- To review and summarize existing studies on AR positivity rates in TNBC patients.
- To consolidate findings on the effects of androgens in TNBC cell lines.
- To investigate the biological significance of AR in TNBC.
Main Methods:
- Systematic review of literature assessing AR positivity in TNBC patient cohorts.
- Analysis of in vitro studies examining androgenic effects on TNBC cell lines.
- Examination of clinical data and survival analyses related to AR expression in TNBC.
Main Results:
- Reported rates of AR positivity in TNBC vary widely (0-53%), likely due to methodological differences in AR analysis.
- Most cell line studies indicate androgens promote TNBC proliferation.
- Preliminary clinical data suggest AR antagonists may improve outcomes for AR-positive TNBC patients.
Conclusions:
- Conflicting evidence exists regarding AR's role in TNBC: cell line studies suggest proliferation promotion, while some clinical and transfection studies indicate a benign or favorable prognostic role.
- Discrepancies between in vitro and clinical findings highlight the need for further translational research into androgen action mechanisms in TNBC.
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