Androgen receptor in bladder cancer: A promising therapeutic target

There has been a significant progress in the treatment of metastatic urothelial carcinoma in the last few years with the advent of immunotherapy after a long gap of no drug approvals for over 4 decades. While immunotherapy with checkpoint inhibitors has revolutionized the treatment of urothelial car...

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Main Authors: Abhishek Tripathi, Shilpa Gupta
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:Asian Journal of Urology
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Online Access:http://www.sciencedirect.com/science/article/pii/S2214388220300370
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author Abhishek Tripathi
Shilpa Gupta
author_facet Abhishek Tripathi
Shilpa Gupta
author_sort Abhishek Tripathi
collection DOAJ
description There has been a significant progress in the treatment of metastatic urothelial carcinoma in the last few years with the advent of immunotherapy after a long gap of no drug approvals for over 4 decades. While immunotherapy with checkpoint inhibitors has revolutionized the treatment of urothelial carcinoma, unfortunately, only a minority of patients respond to immunotherapy. Treatment options for patients who do not respond and/or progress on immunotherapy are very limited and overall prognosis remains dismal in metastatic urothelial carcinoma. The first targeted therapy targeting the fibroblast growth factor receptor (FGFR) was recently approved for bladder cancer, but it is effective only in select patients harboring the FGFR2 and FGFR 3 mutations. Antibody drug conjugates like enfortumab vedotin have shown promising activity in clinical trials. Development of novel targeted therapies remains an area of investigation and an unmet need in bladder cancer. Exploitation of androgen receptor (AR) is a potential strategy for targeted drug development in bladder cancer. A significant proportion of urothelial carcinoma patients express AR irrespective of gender. AR signaling in urothelial carcinoma has been linked to progression through multiple mechanisms, including activation of human epidermal growth factor receptor-2 (EGFR or HER-2) signaling and epithelial to mesenchymal transition (EMT). Furthermore, AR is enriched in the luminal papillary mRNA subtype of urothelial carcinoma and also mediates resistance to cisplatin-based chemotherapy. Preclinical evidence suggests that AR inhibition can successfully inhibit urothelial carcinoma growth as monotherapy and is synergistic with cisplatin-based chemotherapy. We review the preclinical and clinical evidence supporting the putative role of AR signaling in urothelial carcinoma pathogenesis, progression and its role as a novel therapeutic target and future directions.
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spelling doaj-art-e9cf4a04d79a43a8a6d6c20d41cfbbc72025-08-20T03:24:53ZengElsevierAsian Journal of Urology2214-38822020-07-017328429010.1016/j.ajur.2020.05.011Androgen receptor in bladder cancer: A promising therapeutic targetAbhishek Tripathi0Shilpa Gupta1Section of Hematology Oncology, University of Oklahoma Stephenson Cancer Center, Oklahoma City, OK, USADepartment of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH, USA; Corresponding author.There has been a significant progress in the treatment of metastatic urothelial carcinoma in the last few years with the advent of immunotherapy after a long gap of no drug approvals for over 4 decades. While immunotherapy with checkpoint inhibitors has revolutionized the treatment of urothelial carcinoma, unfortunately, only a minority of patients respond to immunotherapy. Treatment options for patients who do not respond and/or progress on immunotherapy are very limited and overall prognosis remains dismal in metastatic urothelial carcinoma. The first targeted therapy targeting the fibroblast growth factor receptor (FGFR) was recently approved for bladder cancer, but it is effective only in select patients harboring the FGFR2 and FGFR 3 mutations. Antibody drug conjugates like enfortumab vedotin have shown promising activity in clinical trials. Development of novel targeted therapies remains an area of investigation and an unmet need in bladder cancer. Exploitation of androgen receptor (AR) is a potential strategy for targeted drug development in bladder cancer. A significant proportion of urothelial carcinoma patients express AR irrespective of gender. AR signaling in urothelial carcinoma has been linked to progression through multiple mechanisms, including activation of human epidermal growth factor receptor-2 (EGFR or HER-2) signaling and epithelial to mesenchymal transition (EMT). Furthermore, AR is enriched in the luminal papillary mRNA subtype of urothelial carcinoma and also mediates resistance to cisplatin-based chemotherapy. Preclinical evidence suggests that AR inhibition can successfully inhibit urothelial carcinoma growth as monotherapy and is synergistic with cisplatin-based chemotherapy. We review the preclinical and clinical evidence supporting the putative role of AR signaling in urothelial carcinoma pathogenesis, progression and its role as a novel therapeutic target and future directions.http://www.sciencedirect.com/science/article/pii/S2214388220300370Androgen receptorUrothelial carcinomaBladder cancerTargeted therapyEnzalutamideCisplatin
spellingShingle Abhishek Tripathi
Shilpa Gupta
Androgen receptor in bladder cancer: A promising therapeutic target
Asian Journal of Urology
Androgen receptor
Urothelial carcinoma
Bladder cancer
Targeted therapy
Enzalutamide
Cisplatin
title Androgen receptor in bladder cancer: A promising therapeutic target
title_full Androgen receptor in bladder cancer: A promising therapeutic target
title_fullStr Androgen receptor in bladder cancer: A promising therapeutic target
title_full_unstemmed Androgen receptor in bladder cancer: A promising therapeutic target
title_short Androgen receptor in bladder cancer: A promising therapeutic target
title_sort androgen receptor in bladder cancer a promising therapeutic target
topic Androgen receptor
Urothelial carcinoma
Bladder cancer
Targeted therapy
Enzalutamide
Cisplatin
url http://www.sciencedirect.com/science/article/pii/S2214388220300370
work_keys_str_mv AT abhishektripathi androgenreceptorinbladdercancerapromisingtherapeutictarget
AT shilpagupta androgenreceptorinbladdercancerapromisingtherapeutictarget