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Toward improving androgen receptor-targeted therapies in male-dominant hepatocellular carcinoma

Journal

DRUG DISCOVERY TODAY
Volume 26, Issue 6, Pages 1539-1546

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2021.02.001

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Funding

  1. NIH [R01 DK124897, R01 GM133198, P30 CA072720]

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Hepatocellular carcinoma (HCC) is the main type of liver cancer and a significant global cause of cancer-related mortality. The androgen receptor (AR) is a key male hormone receptor that plays a role in HCC development and treatment responses, but current clinical trials with AR-targeted agents have not shown survival benefits as expected.
Hepatocellular carcinoma (HCC) is the predominant form of liver cancer and a leading cause of cancer deaths worldwide. HCC is a male-dominant cancer with a male:female ratio of up to 7:1. The androgen receptor (AR) is the male hormone receptor known as a major oncogenic driver of prostate cancer. Although AR has been linked to the sexual dimorphism of HCC, clinical trials with AR-targeted agents failed to generate survival benefits. Recent studies provide new insights into the role of AR in liver tumorigenesis and therapeutic responses. Herein, we review current understanding of AR signaling in HCC and feedback mechanisms that limit response to AR blockade. New AR-targeting strategies that might improve outcomes in HCC therapies are also discussed.

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