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Updated: Jun 27, 2026

09:29
Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Androgen Receptor Expression and T-Lymphocyte Infiltration as Prognostic Indicators in Triple-Negative Breast Cancer:
Olga Milbrandt1, Mateusz Wichtowski2, Justyna Marcinkowska3
1Department of Chemotherapy, Institute of Oncology, Poznan University of Medical Sciences, 60-569 Poznan, Poland.
Biomedicines
|June 26, 2026
Summary
Androgen receptor (AR) expression in triple-negative breast cancer (TNBC) is linked to immune responses, specifically reduced CD8+ T-cell infiltration in AR-high tumors. Further research is needed to confirm survival associations.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Triple-negative breast cancer (TNBC) is a heterogeneous subtype with limited predictive biomarkers.
- Understanding immune microenvironment and potential markers like androgen receptor (AR) is crucial for TNBC.
Purpose of the Study:
- To investigate the clinicopathological associations of AR expression and immune markers (sTILs, CD4+, CD8+, CD4/CD8 ratio) in TNBC.
- To explore the relationship between these markers and 3-year overall survival (OS) in TNBC patients.
Main Methods:
- Retrospective analysis of 86 treatment-naïve TNBC patients.
- Immunohistochemical assessment of AR and CD4/CD8 ratio; H&E scoring of stromal tumor-infiltrating lymphocytes (sTILs).
- Survival analysis using multivariable Cox regression for 3-year OS in stages I-III.
Main Results:
- High AR expression (≥10%) was observed in 23% of TNBC tumors.
- High AR expression correlated with lower CD8+ T-cell infiltration and lower tumor grade.
- No statistically significant independent associations were found between AR, immune markers, and 3-year OS, limited by low event counts.
Conclusions:
- AR status is associated with the tumor immune microenvironment, particularly reduced CD8+ infiltration in AR-high TNBC.
- Distinct AR-immune phenotypes may exist in TNBC.
- Larger prospective studies are required to validate prognostic implications and therapeutic potential due to limited survival data.