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Constitutively Active Androgen Receptor in Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is the predominant type of liver cancer and a leading cause of cancer-related death globally. It is also a sexually dimorphic disease with a male predominance both in HCC and in its precursors, non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NA...

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Autores principales: Montgomery, Emma J., Xing, Enming, Campbell, Moray J., Li, Pui-Kai, Blachly, James S., Tsung, Allan, Coss, Christopher C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699340/
https://www.ncbi.nlm.nih.gov/pubmed/36430245
http://dx.doi.org/10.3390/ijms232213768
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author Montgomery, Emma J.
Xing, Enming
Campbell, Moray J.
Li, Pui-Kai
Blachly, James S.
Tsung, Allan
Coss, Christopher C.
author_facet Montgomery, Emma J.
Xing, Enming
Campbell, Moray J.
Li, Pui-Kai
Blachly, James S.
Tsung, Allan
Coss, Christopher C.
author_sort Montgomery, Emma J.
collection PubMed
description Hepatocellular carcinoma (HCC) is the predominant type of liver cancer and a leading cause of cancer-related death globally. It is also a sexually dimorphic disease with a male predominance both in HCC and in its precursors, non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH). The role of the androgen receptor (AR) in HCC has been well documented; however, AR-targeted therapies have failed to demonstrate efficacy in HCC. Building upon understandings of AR in prostate cancer (PCa), this review examines the role of AR in HCC, non-androgen-mediated mechanisms of induced AR expression, the existence of AR splice variants (AR-SV) in HCC and concludes by surveying current AR-targeted therapeutic approaches in PCa that show potential for efficacy in HCC in light of AR-SV expression.
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spelling pubmed-96993402022-11-26 Constitutively Active Androgen Receptor in Hepatocellular Carcinoma Montgomery, Emma J. Xing, Enming Campbell, Moray J. Li, Pui-Kai Blachly, James S. Tsung, Allan Coss, Christopher C. Int J Mol Sci Review Hepatocellular carcinoma (HCC) is the predominant type of liver cancer and a leading cause of cancer-related death globally. It is also a sexually dimorphic disease with a male predominance both in HCC and in its precursors, non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH). The role of the androgen receptor (AR) in HCC has been well documented; however, AR-targeted therapies have failed to demonstrate efficacy in HCC. Building upon understandings of AR in prostate cancer (PCa), this review examines the role of AR in HCC, non-androgen-mediated mechanisms of induced AR expression, the existence of AR splice variants (AR-SV) in HCC and concludes by surveying current AR-targeted therapeutic approaches in PCa that show potential for efficacy in HCC in light of AR-SV expression. MDPI 2022-11-09 /pmc/articles/PMC9699340/ /pubmed/36430245 http://dx.doi.org/10.3390/ijms232213768 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Montgomery, Emma J.
Xing, Enming
Campbell, Moray J.
Li, Pui-Kai
Blachly, James S.
Tsung, Allan
Coss, Christopher C.
Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title_full Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title_fullStr Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title_full_unstemmed Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title_short Constitutively Active Androgen Receptor in Hepatocellular Carcinoma
title_sort constitutively active androgen receptor in hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699340/
https://www.ncbi.nlm.nih.gov/pubmed/36430245
http://dx.doi.org/10.3390/ijms232213768
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