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Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors
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 immuno...
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Published in: | Biomedicines 2024-05, Vol.12 (5), p.957 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | 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;
< 0.0001) in urothelial carcinoma; advanced pT (
< 0.0001), high tumor grade (
< 0.0001), nodal metastasis (
< 0.0001), and reduced survival (
= 0.0024) in invasive breast carcinoma; high pT (
< 0.0001) and grade (
< 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (
= 0.0055) as well as high grade (
< 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. |
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ISSN: | 2227-9059 2227-9059 |
DOI: | 10.3390/biomedicines12050957 |