Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors

Author:

Viehweger Florian1,Hoop Jennifer1,Tinger Lisa-Marie1,Bernreuther Christian1,Büscheck Franziska1,Clauditz Till S.1ORCID,Hinsch Andrea1,Jacobsen Frank12,Luebke Andreas M.1ORCID,Steurer Stefan1,Hube-Magg Claudia1ORCID,Kluth Martina1,Marx Andreas H.3,Krech Till14,Lebok Patrick14ORCID,Fraune Christoph14,Burandt Eike1,Sauter Guido1,Simon Ronald1ORCID,Minner Sarah1

Affiliation:

1. Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

2. Pathologie-Hamburg, Labor Lademannbogen Medizinisches Versorgungszentrum (MVZ) GmbH, 22339 Hamburg, Germany

3. Department of Pathology, Academic Hospital Fuerth, 90766 Fuerth, Germany

4. Institute of Pathology, Clinical Center Osnabrueck, 49076 Osnabrueck, Germany

Abstract

Androgen receptor (AR) is a transcription factor expressed in various normal tissues and is a therapeutic target for prostate and possibly other cancers. A TMA containing 18,234 samples from 141 different tumor types/subtypes and 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. AR positivity was found in 116 tumor types including 66 tumor types (46.8%) with ≥1 strongly positive tumor. Moderate/strong AR positivity was detected in testicular sex cord-stromal tumors (93.3–100%) and neoplasms of the prostate (79.3–98.7%), breast (25.0–75.5%), other gynecological tumors (0.9–100%), kidney (5.0–44.1%), and urinary bladder (5.4–24.2%). Low AR staining was associated with advanced tumor stage (pTa versus pT2-4; p < 0.0001) in urothelial carcinoma; advanced pT (p < 0.0001), high tumor grade (p < 0.0001), nodal metastasis (p < 0.0001), and reduced survival (p = 0.0024) in invasive breast carcinoma; high pT (p < 0.0001) and grade (p < 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (p = 0.0055) as well as high grade (p < 0.05) in papillary RCC. AR staining was unrelated to histopathological/clinical features in 157 endometrial carcinomas and in 221 ovarian carcinomas. Our data suggest a limited role of AR immunohistochemistry for tumor distinction and a prognostic role in breast and clear cell RCC and highlight tumor entities that might benefit from AR-targeted therapy.

Publisher

MDPI AG

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