Expression of the Androgen Receptor and its Correlation with Molecular Subtypes in 980 Chinese Breast Cancer Patients

Author:

Qi Ji-ping1,Yang You-lin2,Zhu Hong1,Wang Jianmin3,Jia Ying1,Liu Na1,Song Yue-jia1,Zan Li-kun1,Zhang Xu1,Zhou Min1,Gu Yun-he1,Liu Tao1,Hicks David G.4,Tang Ping4

Affiliation:

1. Department of Pathology, First Clinical Hospital, Harbin Medical University, Harbin 150001, PR China.

2. Department of Digestive Systems, First Clinical Hospital, Harbin Medical University, Harbin 150001, PR China.

3. RTI Health Solution, Research Triangle Park, NC.

4. Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York 14642, USA.

Abstract

Background Recent studies have shown that androgen displays an inhibitory effect on breast cancer cell lines that express androgen receptor (AR) but not estrogen receptor (ER) and progesterone receptor (PR). We have previously reported that approximately 1/3 of ER negative high grade invasive ductal carcinomas express AR. Thus, AR can serve as a potential therapeutic target for this group of patients. Aim Here we investigated AR expression patterns in 980 consecutive breast carcinomas. Results We found that (1) AR was expressed more frequently (77%) than ER (61%) and PR (60%) in breast carcinomas; (2) AR expression was associated with ER and PR expression ( P < 0.0001), small tumor size ( P = 0.0324) and lower Ki-67 expression ( P = 0.0013); (3) AR expression was found in 65% of ER negative tumors; (4) AR expression was associated with PR and Ki-67 in ER negative tumors, but not in ER positive tumors; (5) AR expression was higher in ER positive subtypes (Luminal A, Luminal B and Luminal HER2 subtypes, 80%-86%) and lower in ER negative subtypes [HER2, triple negative (TN), and TN EFGR positive subtypes; 52%-66%], with over 50% of TN tumors expressing AR. Conclusion More breast carcinomas express AR than ER and PR, including significant numbers of ER negative and TN tumors, for which AR could serve as a potential therapeutic target.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology

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